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Question 1
Correct
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You are evaluating a different patient's visual acuity (VA) using a Snellen chart. This patient's uncorrected visual acuity (UCVA) is superior to 'normal vision' in the right eye (OD) and only half as good as 'normal vision' in the left eye (OS).
Please provide the appropriate visual acuity format for this patient using the following format:
OD x/y a/b OSYour Answer: OD 6/4 6/12 OS
Explanation:Evaluating visual acuity is a crucial aspect of an eye exam, with a VA of 6/4 indicating superior vision compared to the norm. To determine the best corrected visual acuity, a pinhole test can be utilized.
Typically, a VA of 6/6 is considered standard vision. The numerator denotes the distance (in meters) between the individual and the test chart in optimal lighting conditions. The denominator signifies the distance required for someone with 6/6 vision to view the same line.
By minimizing optic aberrations and temporarily eliminating refractive errors, the pinhole test can provide the most optimal visual acuity achievable with glasses when viewed in good lighting.
A gradual decline in vision is a prevalent issue among the elderly population, leading them to seek guidance from healthcare providers. This condition can be attributed to various causes, including cataracts and age-related macular degeneration. Both of these conditions can cause a gradual loss of vision over time, making it difficult for individuals to perform daily activities such as reading, driving, and recognizing faces. As a result, it is essential for individuals experiencing a decline in vision to seek medical attention promptly to receive appropriate treatment and prevent further deterioration.
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This question is part of the following fields:
- Neurological System
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Question 2
Incorrect
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A 33-year-old female comes to see you with a complaint of right wrist pain that has been bothering her for the past two months. She mentions having difficulty buttoning up her clothes with her right hand. During your examination, you observe that she struggles to pick up a pen with her index finger and thumb, indicating impairment of her pincer grip. Based on these findings, you suspect that she may have sustained damage to her anterior interosseous nerve.
What muscle is innervated by this nerve?Your Answer: Abductor pollicis longus
Correct Answer: Flexor pollicis longus
Explanation:The flexor pollicis longus muscle is innervated by the anterior interosseous nerve, which is a branch of the median nerve. This nerve also innervates the pronator quadratus and the radial half of the flexor digitorum profundus muscles. If this nerve is damaged, it can result in weakness of the pincer grip, as observed in the patient. The ulnar nerve innervates the adductor pollicis muscle, while the radial nerve innervates the abductor pollicis longus muscle. The tibial nerve innervates the flexor digitorum brevis muscle.
The anterior interosseous nerve is a branch of the median nerve that supplies the deep muscles on the front of the forearm, excluding the ulnar half of the flexor digitorum profundus. It runs alongside the anterior interosseous artery along the anterior of the interosseous membrane of the forearm, between the flexor pollicis longus and flexor digitorum profundus. The nerve supplies the whole of the flexor pollicis longus and the radial half of the flexor digitorum profundus, and ends below in the pronator quadratus and wrist joint. The anterior interosseous nerve innervates 2.5 muscles, namely the flexor pollicis longus, pronator quadratus, and the radial half of the flexor digitorum profundus. These muscles are located in the deep level of the anterior compartment of the forearm.
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This question is part of the following fields:
- Neurological System
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Question 3
Incorrect
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A 25 year old male arrives at the Emergency Department after being struck in the back of the head with a baseball bat. He reports a headache and has a laceration on his occiput. He is alert and oriented, following commands and able to provide a detailed description of the incident.
What is his Glasgow coma scale (GCS)?Your Answer: 10
Correct Answer: 15
Explanation:The GCS score for this patient is 654, which stands for Motor (6 points), Verbal (5 points), and Eye opening (4 points). This scoring system is used to evaluate a patient’s level of consciousness by assessing their response to voice, eye movements, and motor function.
GCS is frequently used in patients with head injuries to monitor changes in their neurological status, which may indicate swelling or bleeding.
In this case, the patient’s eyes are open (4 out of 4), she is fully oriented in time, place, and person (5 out of 5), and she is able to follow commands (6 out of 6).
Understanding the Glasgow Coma Scale for Adults
The Glasgow Coma Scale (GCS) is a tool used to assess the level of consciousness in adults who have suffered a brain injury or other neurological condition. It is based on three components: motor response, verbal response, and eye opening. Each component is scored on a scale from 1 to 6, with a higher score indicating a better level of consciousness.
The motor response component assesses the patient’s ability to move in response to stimuli. A score of 6 indicates that the patient is able to obey commands, while a score of 1 indicates no movement at all.
The verbal response component assesses the patient’s ability to communicate. A score of 5 indicates that the patient is fully oriented, while a score of 1 indicates no verbal response at all.
The eye opening component assesses the patient’s ability to open their eyes. A score of 4 indicates that the patient is able to open their eyes spontaneously, while a score of 1 indicates no eye opening at all.
The GCS score is expressed as a combination of the scores from each component, with the motor response score listed first, followed by the verbal response score, and then the eye opening score. For example, a GCS score of 13, M5 V4 E4 at 21:30 would indicate that the patient had a motor response score of 5, a verbal response score of 4, and an eye opening score of 4 at 9:30 pm.
Overall, the Glasgow Coma Scale is a useful tool for healthcare professionals to assess the level of consciousness in adults with neurological conditions.
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This question is part of the following fields:
- Neurological System
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Question 4
Incorrect
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A 46-year-old man comes to the clinic complaining of bilateral sciatica and partial urinary incontinence. Upon conducting a comprehensive examination and lumbosacral magnetic resonance imaging, the diagnosis of cauda equina syndrome is confirmed at the L2 level.
What is the most probable finding to be observed during the examination?Your Answer: Hyperreflexic knee jerk reflex
Correct Answer: S2-S4 anaesthesia
Explanation:Lesions in the lower lumbar region cannot result in upper motor neuron signs because the spinal cord terminates at L1.
The spinal cord is a central structure located within the vertebral column that provides it with structural support. It extends rostrally to the medulla oblongata of the brain and tapers caudally at the L1-2 level, where it is anchored to the first coccygeal vertebrae by the filum terminale. The cord is characterised by cervico-lumbar enlargements that correspond to the brachial and lumbar plexuses. It is incompletely divided into two symmetrical halves by a dorsal median sulcus and ventral median fissure, with grey matter surrounding a central canal that is continuous with the ventricular system of the CNS. Afferent fibres entering through the dorsal roots usually terminate near their point of entry but may travel for varying distances in Lissauer’s tract. The key point to remember is that the anatomy of the cord will dictate the clinical presentation in cases of injury, which can be caused by trauma, neoplasia, inflammatory diseases, vascular issues, or infection.
One important condition to remember is Brown-Sequard syndrome, which is caused by hemisection of the cord and produces ipsilateral loss of proprioception and upper motor neuron signs, as well as contralateral loss of pain and temperature sensation. Lesions below L1 tend to present with lower motor neuron signs. It is important to keep a clinical perspective in mind when revising CNS anatomy and to understand the ways in which the spinal cord can become injured, as this will help in diagnosing and treating patients with spinal cord injuries.
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This question is part of the following fields:
- Neurological System
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Question 5
Incorrect
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A 38-year-old man visits his doctor with worries of having spinal muscular atrophy, as his father has been diagnosed with the condition. He asks for a physical examination.
What physical exam finding is indicative of the characteristic pattern observed in this disorder?Your Answer: Increased reflexes
Correct Answer: Reduced reflexes
Explanation:Lower motor neuron lesions, such as spinal muscular atrophy, result in reduced reflexes and tone. Babinski’s sign is negative in these cases. Increased reflexes and tone are indicative of an upper motor neuron cause of symptoms, which may be seen in conditions such as stroke or Parkinson’s disease. Therefore, normal reflexes and tone are also incorrect findings in lower motor neuron lesions.
The spinal cord is a central structure located within the vertebral column that provides it with structural support. It extends rostrally to the medulla oblongata of the brain and tapers caudally at the L1-2 level, where it is anchored to the first coccygeal vertebrae by the filum terminale. The cord is characterised by cervico-lumbar enlargements that correspond to the brachial and lumbar plexuses. It is incompletely divided into two symmetrical halves by a dorsal median sulcus and ventral median fissure, with grey matter surrounding a central canal that is continuous with the ventricular system of the CNS. Afferent fibres entering through the dorsal roots usually terminate near their point of entry but may travel for varying distances in Lissauer’s tract. The key point to remember is that the anatomy of the cord will dictate the clinical presentation in cases of injury, which can be caused by trauma, neoplasia, inflammatory diseases, vascular issues, or infection.
One important condition to remember is Brown-Sequard syndrome, which is caused by hemisection of the cord and produces ipsilateral loss of proprioception and upper motor neuron signs, as well as contralateral loss of pain and temperature sensation. Lesions below L1 tend to present with lower motor neuron signs. It is important to keep a clinical perspective in mind when revising CNS anatomy and to understand the ways in which the spinal cord can become injured, as this will help in diagnosing and treating patients with spinal cord injuries.
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This question is part of the following fields:
- Neurological System
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Question 6
Incorrect
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After spending 8 weeks in a plaster cast on his left leg, John, a 25-year-old male, visits the clinic to have it removed. During the examination, it is observed that his left foot is in a plantar flexed position, indicating foot drop. Which nerve is typically impacted, resulting in foot drop?
Your Answer: Obturator nerve
Correct Answer: Common peroneal nerve
Explanation:Footdrop, which is impaired dorsiflexion of the ankle, can be caused by a lesion of the common peroneal nerve. This nerve is a branch of the sciatic nerve and divides into the deep and superficial peroneal nerves after wrapping around the neck of the fibula. The deep peroneal nerve is responsible for innervating muscles that control dorsiflexion of the foot, such as the tibialis anterior, extensor hallucis longus, and extensor digitorum longus. Damage to the common or deep peroneal nerve can result in weakness or paralysis of these muscles, leading to unopposed plantar flexion of the foot. The superficial peroneal nerve, on the other hand, innervates muscles that evert the foot. Other nerves that innervate muscles in the lower limb include the femoral nerve, which controls hip flexion and knee extension, the tibial nerve, which mainly controls plantar flexion and inversion of the foot, and the obturator nerve, which mainly controls thigh adduction.
The common peroneal nerve originates from the dorsal divisions of the sacral plexus, specifically from L4, L5, S1, and S2. This nerve provides sensation to the skin and fascia of the anterolateral surface of the leg and dorsum of the foot, as well as innervating the muscles of the anterior and peroneal compartments of the leg, extensor digitorum brevis, and the knee, ankle, and foot joints. It is located laterally within the sciatic nerve and passes through the lateral and proximal part of the popliteal fossa, under the cover of biceps femoris and its tendon, to reach the posterior aspect of the fibular head. The common peroneal nerve divides into the deep and superficial peroneal nerves at the point where it winds around the lateral surface of the neck of the fibula in the body of peroneus longus, approximately 2 cm distal to the apex of the head of the fibula. It is palpable posterior to the head of the fibula. The nerve has several branches, including the nerve to the short head of biceps, articular branch (knee), lateral cutaneous nerve of the calf, and superficial and deep peroneal nerves at the neck of the fibula.
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This question is part of the following fields:
- Neurological System
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Question 7
Incorrect
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A 23-year-old man is in a physical altercation resulting in a skull fracture and damage to the middle meningeal artery. After undergoing a craniotomy, the bleeding from the artery is successfully stopped through ligation near its origin. What sensory impairment is the patient most likely to experience after the operation?
Your Answer: Loss of sensation from the ipsilateral side of the tongue
Correct Answer: Parasthesia of the ipsilateral external ear
Explanation:The middle meningeal artery is in close proximity to the auriculotemporal nerve, which could potentially be harmed in this situation. This nerve is responsible for providing sensation to the outer ear and the outer layer of the tympanic membrane. The C2,3 roots innervate the jaw angle and would not be impacted. The glossopharyngeal nerve is responsible for supplying the tongue.
The Middle Meningeal Artery: Anatomy and Clinical Significance
The middle meningeal artery is a branch of the maxillary artery, which is one of the two terminal branches of the external carotid artery. It is the largest of the three arteries that supply the meninges, the outermost layer of the brain. The artery runs through the foramen spinosum and supplies the dura mater. It is located beneath the pterion, where the skull is thin, making it vulnerable to injury. Rupture of the artery can lead to an Extradural hematoma.
In the dry cranium, the middle meningeal artery creates a deep indentation in the calvarium. It is intimately associated with the auriculotemporal nerve, which wraps around the artery. This makes the two structures easily identifiable in the dissection of human cadavers and also easily damaged in surgery.
Overall, understanding the anatomy and clinical significance of the middle meningeal artery is important for medical professionals, particularly those involved in neurosurgery.
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This question is part of the following fields:
- Neurological System
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Question 8
Correct
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A 49-year-old man with a diagnosis of glioblastoma multiforme and resistance to chemotherapy is referred for a craniotomy to remove the mass-occupying lesion. What is the correct sequence of layers the surgeon must pass through, from most superficial to deepest, during the craniotomy which involves creating an opening through the scalp and meninges?
Your Answer: Loose Connective Tissue, Periosteum, Dura Mater, Arachnoid Mater, Pia Mater
Explanation:The outermost layer of the meninges is the dura mater.
To remember the layers of the scalp from superficial to deep, use the acronym SCALP: Skin, Connective tissue, Aponeurosis, Loose connective tissue, Periosteum.
To remember the layers of the meninges from superficial to deep, use the acronym DAP: Dura mater, Arachnoid mater, Pia mater.
The Three Layers of Meninges
The meninges are a group of membranes that cover the brain and spinal cord, providing support to the central nervous system and the blood vessels that supply it. These membranes can be divided into three distinct layers: the dura mater, arachnoid mater, and pia mater.
The outermost layer, the dura mater, is a thick fibrous double layer that is fused with the inner layer of the periosteum of the skull. It has four areas of infolding and is pierced by small areas of the underlying arachnoid to form structures called arachnoid granulations. The arachnoid mater forms a meshwork layer over the surface of the brain and spinal cord, containing both cerebrospinal fluid and vessels supplying the nervous system. The final layer, the pia mater, is a thin layer attached directly to the surface of the brain and spinal cord.
The meninges play a crucial role in protecting the brain and spinal cord from injury and disease. However, they can also be the site of serious medical conditions such as subdural and subarachnoid haemorrhages. Understanding the structure and function of the meninges is essential for diagnosing and treating these conditions.
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This question is part of the following fields:
- Neurological System
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Question 9
Incorrect
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A 16-year-old male comes to the clinic after experiencing a seizure. During the history-taking, he reports that he first noticed shaking in his hand about an hour ago. The shaking continued for a few seconds before he lost consciousness and bit his tongue. He also experienced urinary incontinence. How would you describe this presentation?
Your Answer: Complex seizure
Correct Answer: Partial seizure with secondary generalisation
Explanation:Epilepsy is a neurological condition that causes recurrent seizures. In the UK, around 500,000 people have epilepsy, and two-thirds of them can control their seizures with antiepileptic medication. While epilepsy usually occurs in isolation, certain conditions like cerebral palsy, tuberous sclerosis, and mitochondrial diseases have an association with epilepsy. It’s important to note that seizures can also occur due to other reasons like infection, trauma, or metabolic disturbance.
Seizures can be classified into focal seizures, which start in a specific area of the brain, and generalised seizures, which involve networks on both sides of the brain. Patients who have had generalised seizures may experience biting their tongue or incontinence of urine. Following a seizure, patients typically have a postictal phase where they feel drowsy and tired for around 15 minutes.
Patients who have had their first seizure generally undergo an electroencephalogram (EEG) and neuroimaging (usually a MRI). Most neurologists start antiepileptics following a second epileptic seizure. Antiepileptics are one of the few drugs where it is recommended that we prescribe by brand, rather than generically, due to the risk of slightly different bioavailability resulting in a lowered seizure threshold.
Patients who drive, take other medications, wish to get pregnant, or take contraception need to consider the possible interactions of the antiepileptic medication. Some commonly used antiepileptics include sodium valproate, carbamazepine, lamotrigine, and phenytoin. In case of a seizure that doesn’t terminate after 5-10 minutes, medication like benzodiazepines may be administered to terminate the seizure. If a patient continues to fit despite such measures, they are said to have status epilepticus, which is a medical emergency requiring hospital treatment.
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This question is part of the following fields:
- Neurological System
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Question 10
Incorrect
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A 26-year-old female patient is being evaluated by her GP a couple of weeks after recuperating from an incident. Although most of her injuries have healed, she still cannot utilize the muscles of mastication on the left side of her face. Which cranial nerve is likely to be accountable for this?
Your Answer: Left facial motor nerve (CN VII)
Correct Answer: Left trigeminal motor nerve (CN V)
Explanation:Cranial nerves are a set of 12 nerves that emerge from the brain and control various functions of the head and neck. Each nerve has a specific function, such as smell, sight, eye movement, facial sensation, and tongue movement. Some nerves are sensory, some are motor, and some are both. A useful mnemonic to remember the order of the nerves is Some Say Marry Money But My Brother Says Big Brains Matter Most, with S representing sensory, M representing motor, and B representing both.
In addition to their specific functions, cranial nerves also play a role in various reflexes. These reflexes involve an afferent limb, which carries sensory information to the brain, and an efferent limb, which carries motor information from the brain to the muscles. Examples of cranial nerve reflexes include the corneal reflex, jaw jerk, gag reflex, carotid sinus reflex, pupillary light reflex, and lacrimation reflex. Understanding the functions and reflexes of the cranial nerves is important in diagnosing and treating neurological disorders.
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This question is part of the following fields:
- Neurological System
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Question 11
Incorrect
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A 19-year-old male is brought to the emergency room following ingestion of a significant quantity of cocaine. He is experiencing excessive sweating and heart palpitations. During the examination, his pupils are found to be dilated and he is exhibiting tachycardia and tachypnea.
From which spinal level do the preganglionic neurons of the system responsible for his symptoms originate?Your Answer: Cranial nerves 3,7,9 and 10 and S2-4
Correct Answer: T1-L2/3
Explanation:The lateral horns of grey matter give rise to the preganglionic neurons of the sympathetic nervous system.
Understanding the Autonomic Nervous System
The autonomic nervous system is responsible for regulating involuntary functions in the body, such as heart rate, digestion, and sexual arousal. It is composed of two main components, the sympathetic and parasympathetic nervous systems, as well as a sensory division. The sympathetic division arises from the T1-L2/3 region of the spinal cord and synapses onto postganglionic neurons at paravertebral or prevertebral ganglia. The parasympathetic division arises from cranial nerves and the sacral spinal cord and synapses with postganglionic neurons at parasympathetic ganglia. The sensory division includes baroreceptors and chemoreceptors that monitor blood levels of oxygen, carbon dioxide, and glucose, as well as arterial pressure and the contents of the stomach and intestines.
The autonomic nervous system releases neurotransmitters such as noradrenaline and acetylcholine to achieve necessary functions and regulate homeostasis. The sympathetic nervous system causes fight or flight responses, while the parasympathetic nervous system causes rest and digest responses. Autonomic dysfunction refers to the abnormal functioning of any part of the autonomic nervous system, which can present in many forms and affect any of the autonomic systems. To assess a patient for autonomic dysfunction, a detailed history should be taken, and the patient should undergo a full neurological examination and further testing if necessary. Understanding the autonomic nervous system is crucial in diagnosing and treating autonomic dysfunction.
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This question is part of the following fields:
- Neurological System
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Question 12
Correct
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A 10-month-old girl arrives at the emergency department with cough and nasal congestion. The triage nurse records a temperature of 38.2ºC. Which area of the brain is accountable for the observed physiological anomaly in this infant?
Your Answer: Hypothalamus
Explanation:The hypothalamus is responsible for regulating body temperature, as it controls thermoregulation. It responds to pyrogens produced during infections, which induce the synthesis of prostaglandins that bind to receptors in the hypothalamus and raise body temperature. The cerebellum, limbic system, and pineal gland are not involved in temperature control.
The hypothalamus is a part of the brain that plays a crucial role in maintaining the body’s internal balance, or homeostasis. It is located in the diencephalon and is responsible for regulating various bodily functions. The hypothalamus is composed of several nuclei, each with its own specific function. The anterior nucleus, for example, is involved in cooling the body by stimulating the parasympathetic nervous system. The lateral nucleus, on the other hand, is responsible for stimulating appetite, while lesions in this area can lead to anorexia. The posterior nucleus is involved in heating the body and stimulating the sympathetic nervous system, and damage to this area can result in poikilothermia. Other nuclei include the septal nucleus, which regulates sexual desire, the suprachiasmatic nucleus, which regulates circadian rhythm, and the ventromedial nucleus, which is responsible for satiety. Lesions in the paraventricular nucleus can lead to diabetes insipidus, while lesions in the dorsomedial nucleus can result in savage behavior.
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This question is part of the following fields:
- Neurological System
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Question 13
Incorrect
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Following the discovery of a pituitary tumour in a 32-year-old woman who presented with amenorrhoea, a brain MRI is conducted to fully evaluate the tumour before surgical removal. The results reveal that the tumour is starting to compress the lateral geniculate nucleus of the thalamus.
What kind of symptom would arise from this compression?Your Answer: Expressive aphasia
Correct Answer: Visual impairment
Explanation:Visual impairment can occur as a result of damage to the lateral geniculate nucleus (LGN), which is a part of the thalamus involved in the visual pathway. The LGN receives information from the retina and sends it to the cortex via optic radiations. Although rare, the LGN can be damaged by compression from pituitary tumors or lesions affecting the choroidal arteries. However, damage to the LGN or other parts of the thalamus will not cause auditory impairment, aphasia, or reduced facial sensation. These conditions are typically caused by damage to other regions of the brain.
The Thalamus: Relay Station for Motor and Sensory Signals
The thalamus is a structure located between the midbrain and cerebral cortex that serves as a relay station for motor and sensory signals. Its main function is to transmit these signals to the cerebral cortex, which is responsible for processing and interpreting them. The thalamus is composed of different nuclei, each with a specific function. The lateral geniculate nucleus relays visual signals, while the medial geniculate nucleus transmits auditory signals. The medial portion of the ventral posterior nucleus (VML) is responsible for facial sensation, while the ventral anterior/lateral nuclei relay motor signals. Finally, the lateral portion of the ventral posterior nucleus is responsible for body sensation, including touch, pain, proprioception, pressure, and vibration. Overall, the thalamus plays a crucial role in the transmission of sensory and motor information to the brain, allowing us to perceive and interact with the world around us.
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This question is part of the following fields:
- Neurological System
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Question 14
Incorrect
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A 19-year-old man is trimming some bushes when a tiny piece of foliage gets into his eye, causing it to water. Which component is accountable for transmitting parasympathetic nerve signals to the lacrimal apparatus?
Your Answer: Otic ganglion
Correct Answer: Pterygopalatine ganglion
Explanation:The pterygopalatine ganglion serves as a pathway for the parasympathetic fibers that reach the lacrimal apparatus.
The Lacrimation Reflex
The lacrimation reflex is a response to conjunctival irritation or emotional events. When the conjunctiva is irritated, it sends signals via the ophthalmic nerve to the superior salivary center. From there, efferent signals pass via the greater petrosal nerve (parasympathetic preganglionic fibers) and the deep petrosal nerve (postganglionic sympathetic fibers) to the lacrimal apparatus. The parasympathetic fibers relay in the pterygopalatine ganglion, while the sympathetic fibers do not synapse.
This reflex is important for maintaining the health of the eye by keeping it moist and protecting it from foreign particles. It is also responsible for the tears that are shed during emotional events, such as crying. The lacrimal gland, which produces tears, is innervated by the secretomotor parasympathetic fibers from the pterygopalatine ganglion. The nasolacrimal duct, which carries tears from the eye to the nose, opens anteriorly in the inferior meatus of the nose. Overall, the lacrimal system plays a crucial role in maintaining the health and function of the eye.
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This question is part of the following fields:
- Neurological System
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Question 15
Incorrect
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An 87-year-old man has been admitted to the geriatrics ward due to repeated falls at home. He has been experiencing memory problems for the past 5-10 years and has become increasingly aggressive towards his family. Additionally, he has difficulty with self-care and often becomes disoriented.
During examination, there are no noticeable tremors or walking difficulties. The patient does not exhibit any signs of chorea, hallucinations, or vivid dreams. There are no features of disinhibition, and the patient is able to communicate normally.
What type of abnormality would you expect to see on an MRI scan?Your Answer:
Correct Answer: Atrophy of the cortex and hippocampus
Explanation:Alzheimer’s disease is characterized by widespread cerebral atrophy, primarily affecting the cortex and hippocampus. This results in symptoms such as memory loss, behavioral changes, poor self-care, and getting lost frequently. The cortex is responsible for motor planning and behavioral issues, while the hippocampus is responsible for memory features. Atrophy of the caudate head and putamen is not consistent with Alzheimer’s disease, but rather with Huntington’s disease, which is a genetic disorder characterized by chorea. Atrophy of the frontal and temporal lobes is more consistent with frontotemporal dementia, which presents with greater language and behavioral issues. Hyper-intensity of the substantia nigra and red nuclei is not a feature of Alzheimer’s disease, but rather of Parkinson’s disease, which is characterized by movement issues such as tremors and shuffling gait, as well as hallucinations and sleep disturbances.
Alzheimer’s disease is a type of dementia that gradually worsens over time and is caused by the degeneration of the brain. There are several risk factors associated with Alzheimer’s disease, including increasing age, family history, and certain genetic mutations. The disease is also more common in individuals of Caucasian ethnicity and those with Down’s syndrome.
The pathological changes associated with Alzheimer’s disease include widespread cerebral atrophy, particularly in the cortex and hippocampus. Microscopically, there are cortical plaques caused by the deposition of type A-Beta-amyloid protein and intraneuronal neurofibrillary tangles caused by abnormal aggregation of the tau protein. The hyperphosphorylation of the tau protein has been linked to Alzheimer’s disease. Additionally, there is a deficit of acetylcholine due to damage to an ascending forebrain projection.
Neurofibrillary tangles are a hallmark of Alzheimer’s disease and are partly made from a protein called tau. Tau is a protein that interacts with tubulin to stabilize microtubules and promote tubulin assembly into microtubules. In Alzheimer’s disease, tau proteins are excessively phosphorylated, impairing their function.
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This question is part of the following fields:
- Neurological System
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Question 16
Incorrect
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An 80-year-old female presents to the emergency department after falling two days ago. She is now experiencing double vision and haziness in her right eye. She tripped on a carpet in her living room and hit her head, but did not lose consciousness. She has a medical history of polymyalgia rheumatica, stable angina, bilateral cataract surgeries, and one previous transient ischaemic attack. There is no family history of genetic conditions.
During the examination, she is alert and oriented to time, place, and person. No peripheral focal neurology is found, and Romberg's test is negative. Her right eye has reduced visual acuity, but her pupils are equal and reactive to light, and her eye movements are unimpaired. The conjunctiva is not injected, and ophthalmoscopy shows normal visualization of the retina on the left and difficulty on the right due to light reflecting from behind the iris.
Blood tests reveal an ESR of 34mm/h (1-40mm/h) and CRP of 3 mg/L (<5 mg/L). What is the most likely cause of her visual symptoms?Your Answer:
Correct Answer: Dislocated intraocular lens (IOL)
Explanation:Inherited connective tissue disorders can lead to natural lens dislocation, while replacement lenses may become dislodged after cataract surgery. Temporal arteritis is a rare condition that affects small to medium arteries and is typically accompanied by a headache, blurred vision, and jaw claudication. Transient ischaemic attacks cause focal neurology and resolve within 24 hours. Although rare, complications of cataract surgery can include infection, damage to the capsule, posterior cataract formation, and glaucoma. Lens dislocation can occur due to trauma, uveitis, previous vitreoretinal surgery, or congenital connective tissue disorders such as Marfan’s syndrome. Acute angle-closure crisis, also known as acute glaucoma, presents with a red, painful eye with mid-dilated and poorly reactive pupils.
Causes of Lens Dislocation
Lens dislocation can occur due to various reasons. One of the most common causes is Marfan’s syndrome, which causes the lens to dislocate upwards. Another cause is homocystinuria, which leads to the lens dislocating downwards. Ehlers-Danlos syndrome is also a contributing factor to lens dislocation. Trauma, uveal tumors, and autosomal recessive ectopia lentis are other causes of lens dislocation. It is important to identify the underlying cause of lens dislocation to determine the appropriate treatment plan. Proper diagnosis and management can prevent further complications and improve the patient’s quality of life.
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This question is part of the following fields:
- Neurological System
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Question 17
Incorrect
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A 78-year-old woman with a history of neurosarcoidosis treated with steroids visits her GP complaining of intense facial pain. The pain lasts only a few seconds but is unbearable and worsens with exposure to cold air and touch.
Upon examination, there are no focal neurological signs. However, a few minutes after the examination, she experiences severe pain on her right cheek, which she describes as always being over her right zygoma.
Through which opening in the skull does the affected cranial nerve pass?Your Answer:
Correct Answer: Foramen rotundum
Explanation:The correct answer is Foramen rotundum, as the maxillary nerve passes through this foramen to exit the skull. This nerve is responsible for the sensory innervation of the upper teeth, gums, and palate. The patient’s trigeminal neuralgia is caused by irritation of the right-sided maxillary nerve.
Cribriform plate is not the correct answer, as this area of the skull is where the olfactory nerve passes through to enable the sense of smell.
Foramen ovale is also not the correct answer, as this foramen is where the mandibular nerve exits the skull to provide sensation to the lower face.
Jugular foramen is not the correct answer, as this foramen is where the accessory nerve passes through to innervate the sternocleidomastoid and trapezius muscles.
Cranial nerves are a set of 12 nerves that emerge from the brain and control various functions of the head and neck. Each nerve has a specific function, such as smell, sight, eye movement, facial sensation, and tongue movement. Some nerves are sensory, some are motor, and some are both. A useful mnemonic to remember the order of the nerves is Some Say Marry Money But My Brother Says Big Brains Matter Most, with S representing sensory, M representing motor, and B representing both.
In addition to their specific functions, cranial nerves also play a role in various reflexes. These reflexes involve an afferent limb, which carries sensory information to the brain, and an efferent limb, which carries motor information from the brain to the muscles. Examples of cranial nerve reflexes include the corneal reflex, jaw jerk, gag reflex, carotid sinus reflex, pupillary light reflex, and lacrimation reflex. Understanding the functions and reflexes of the cranial nerves is important in diagnosing and treating neurological disorders.
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This question is part of the following fields:
- Neurological System
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Question 18
Incorrect
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A 32-year-old overweight woman comes to you complaining of a severe headache that is affecting both sides of her head. She also reports blurred vision in her left eye. Upon examination, you notice papilloedema and a CNVI palsy in her left eye. Her blood pressure is 160/100 mmHg, and she is currently taking the combined oral contraceptive pill (COCP). What is the probable diagnosis?
Your Answer:
Correct Answer: Idiopathic intracranial hypertension
Explanation:The correct answer is: Headache, blurred vision, papilloedema, and CNVI palsy in a young, obese female on COCP are highly indicative of idiopathic intracranial hypertension. PKD may lead to hypertension and rupture of a berry aneurysm, but it would present with stroke-like symptoms. The presence of a berry aneurysm on its own would not cause any symptoms. Acute-angle closure glaucoma would present with a painful acute red eye and vomiting.
Understanding Idiopathic Intracranial Hypertension
Idiopathic intracranial hypertension, also known as pseudotumour cerebri, is a medical condition that is commonly observed in young, overweight females. The condition is characterized by a range of symptoms, including headache, blurred vision, and papilloedema, which is usually present. Other symptoms may include an enlarged blind spot and sixth nerve palsy.
There are several risk factors associated with idiopathic intracranial hypertension, including obesity, female sex, pregnancy, and certain drugs such as the combined oral contraceptive pill, steroids, tetracyclines, vitamin A, and lithium.
Management of idiopathic intracranial hypertension may involve weight loss, diuretics such as acetazolamide, and topiramate, which can also cause weight loss in most patients. Repeated lumbar puncture may also be necessary, and surgery may be required to prevent damage to the optic nerve. This may involve optic nerve sheath decompression and fenestration, or a lumboperitoneal or ventriculoperitoneal shunt to reduce intracranial pressure.
It is important to note that if intracranial hypertension is thought to occur secondary to a known cause, such as medication, it is not considered idiopathic. Understanding the risk factors and symptoms associated with idiopathic intracranial hypertension can help individuals seek appropriate medical attention and management.
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This question is part of the following fields:
- Neurological System
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Question 19
Incorrect
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A mother brings her 6-year-old daughter into hospital worried that she is slower than the other girls when standing up. Upon further inquiry, the mother discloses that her daughter walks in an unusual manner and that her grandmother passed away when she was very young. What is the probable cause of the young girl's condition?
Your Answer:
Correct Answer: Mutation in the gene coding for dystrophin
Explanation:Duchenne muscular dystrophy (DMD) is characterised by a waddling gait and Gower’s sign, and follows an X-linked recessive pattern of inheritance. Cystic fibrosis is caused by improper chloride ion channel formation, myasthenia gravis by an autoimmune process against acetylcholine receptors, phenylketonuria by a lack of phenylalanine breakdown, and sickle cell anaemia by a mutation in the gene coding for haemoglobin.
Dystrophinopathies are a group of genetic disorders that are inherited in an X-linked recessive manner. These disorders are caused by mutations in the dystrophin gene located on the X chromosome at position Xp21. Dystrophin is a protein that is part of a larger membrane-associated complex in muscle cells. It connects the muscle membrane to actin, which is a component of the muscle cytoskeleton.
Duchenne muscular dystrophy is a severe form of dystrophinopathy that is caused by a frameshift mutation in the dystrophin gene. This mutation results in the loss of one or both binding sites, leading to progressive proximal muscle weakness that typically begins around the age of 5 years. Children with Duchenne muscular dystrophy may also exhibit calf pseudohypertrophy and Gower’s sign, which is when they use their arms to stand up from a squatted position. Approximately 30% of patients with Duchenne muscular dystrophy also have intellectual impairment.
In contrast, Becker muscular dystrophy is a milder form of dystrophinopathy that typically develops after the age of 10 years. It is caused by a non-frameshift insertion in the dystrophin gene, which preserves both binding sites. Intellectual impairment is much less common in individuals with Becker muscular dystrophy.
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This question is part of the following fields:
- Neurological System
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Question 20
Incorrect
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A 75-year-old man with a long-standing history of type 2 diabetes mellitus presents to his physician with an inability to walk. The patient has a history of chronic kidney disease, diabetic retinopathy and a prior myocardial infarction treated via a stent. The patient admits to a recent loss of sensation in the lower limbs and is found to also have associated motor neuropathy. Complications of his chronic disease are found to be the cause of his gait problems.
What findings would be expected during examination of the lower limbs?Your Answer:
Correct Answer: Decreased reflexes, fasciculations, decreased tone
Explanation:When there is a lower motor neuron lesion, there is a reduction in everything, including reflexes, tone, and power. Fasciculations are also a common feature. Motor neuropathy caused by diabetes is a form of peripheral neuropathy, which typically presents with lower motor neuron symptoms. On the other hand, an upper motor neuron lesion is characterized by increased tone, reflexes, and weakness. A mixed picture may occur when there are both upper and lower motor neuron signs present. For example, Babinski positive, increased reflexes, and decreased tone indicate a combination of upper and lower motor neuron lesions. Similarly, decreased tone, decreased reflexes, and clonus suggest a mixed picture, with the clonus being an upper motor neuron sign. Conversely, increased tone, decreased reflexes, and clonus also indicate a mixed picture, with the increased tone and clonus being upper motor neuron signs and the decreased reflexes being a lower motor neuron sign.
The spinal cord is a central structure located within the vertebral column that provides it with structural support. It extends rostrally to the medulla oblongata of the brain and tapers caudally at the L1-2 level, where it is anchored to the first coccygeal vertebrae by the filum terminale. The cord is characterised by cervico-lumbar enlargements that correspond to the brachial and lumbar plexuses. It is incompletely divided into two symmetrical halves by a dorsal median sulcus and ventral median fissure, with grey matter surrounding a central canal that is continuous with the ventricular system of the CNS. Afferent fibres entering through the dorsal roots usually terminate near their point of entry but may travel for varying distances in Lissauer’s tract. The key point to remember is that the anatomy of the cord will dictate the clinical presentation in cases of injury, which can be caused by trauma, neoplasia, inflammatory diseases, vascular issues, or infection.
One important condition to remember is Brown-Sequard syndrome, which is caused by hemisection of the cord and produces ipsilateral loss of proprioception and upper motor neuron signs, as well as contralateral loss of pain and temperature sensation. Lesions below L1 tend to present with lower motor neuron signs. It is important to keep a clinical perspective in mind when revising CNS anatomy and to understand the ways in which the spinal cord can become injured, as this will help in diagnosing and treating patients with spinal cord injuries.
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This question is part of the following fields:
- Neurological System
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Question 21
Incorrect
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A 62-year-old man comes to the emergency department with recent involuntary movements. During the examination, it is observed that he has unmanageable thrashing movements of his left arm and leg, which cannot be diverted. A CT scan reveals a fresh acute infarct.
What part of the brain has been impacted by this infarct, causing these symptoms?Your Answer:
Correct Answer: Subthalamic nucleus
Explanation:Lesions of the subthalamic nucleus (STN) within the basal ganglia can result in a hemiballismus, characterized by uncontrollable thrashing movements. The STN plays a role in unconscious motor control by providing excitatory input to the globus pallidus internus (GPi), which then acts in an inhibitory way on motor outflow from the cortex. When the STN is damaged, there is less activity within the GPi and relative hyperactivity of the motor cortex, leading to excessive movements.
In contrast, lesions of the caudate nucleus within the basal ganglia can cause behavioral changes and agitation. The caudate processes motor information from the cortex and provides an excitatory input to the globus pallidus externus (GPe), which then has an excitatory input to the STN. Lesions of the caudate result in motor hyperactivity, but this manifests as a restless state rather than uncontrolled movements. The caudate also plays a role in the neural circuits underlying goal-directed behaviors, and lesions can result in personality and behavioral changes.
Lesions of the medial pons can cause hemiplegia and hemisensory loss or locked-in syndrome, depending on the level of disruption to the motor and sensory pathways. Lesions above the level of the trigeminal and facial motor nuclei can result in a full locked-in syndrome, while lesions below these nuclei result in hemiplegia and hemisensory loss but with preservation of facial sensation and movement.
Lesions of the substantia nigra result in Parkinsonism, as the dopaminergic neurons of the substantia nigra have an inhibitory effect on the outflow of the striatum. This prevents motor information from leaving the cortex, resulting in the bradykinesia characteristic of Parkinsonism.
Thalamic lesions most commonly cause hemisensory loss, as the thalamus acts as a sensory gateway that allows processing of sensory information before relaying it to the relevant primary cortex. Lesions disrupt this pathway and prevent information from reaching the cortex.
Brain lesions can be localized based on the neurological disorders or features that are present. The gross anatomy of the brain can provide clues to the location of the lesion. For example, lesions in the parietal lobe can result in sensory inattention, apraxias, astereognosis, inferior homonymous quadrantanopia, and Gerstmann’s syndrome. Lesions in the occipital lobe can cause homonymous hemianopia, cortical blindness, and visual agnosia. Temporal lobe lesions can result in Wernicke’s aphasia, superior homonymous quadrantanopia, auditory agnosia, and prosopagnosia. Lesions in the frontal lobes can cause expressive aphasia, disinhibition, perseveration, anosmia, and an inability to generate a list. Lesions in the cerebellum can result in gait and truncal ataxia, intention tremor, past pointing, dysdiadokinesis, and nystagmus.
In addition to the gross anatomy, specific areas of the brain can also provide clues to the location of a lesion. For example, lesions in the medial thalamus and mammillary bodies of the hypothalamus can result in Wernicke and Korsakoff syndrome. Lesions in the subthalamic nucleus of the basal ganglia can cause hemiballism, while lesions in the striatum (caudate nucleus) can result in Huntington chorea. Parkinson’s disease is associated with lesions in the substantia nigra of the basal ganglia, while lesions in the amygdala can cause Kluver-Bucy syndrome, which is characterized by hypersexuality, hyperorality, hyperphagia, and visual agnosia. By identifying these specific conditions, doctors can better localize brain lesions and provide appropriate treatment.
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This question is part of the following fields:
- Neurological System
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Question 22
Incorrect
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A 60-year-old man visits an after-hours medical facility in the late evening with a complaint of a severe headache that is focused around his left eye. He mentions experiencing haloes in his vision and difficulty seeing clearly. The patient has a medical history of hypertension and diabetes. During the examination, the sclera appears red, and the cornea is hazy with a dilated pupil.
What condition is the most probable diagnosis?Your Answer:
Correct Answer: Acute closed-angle glaucoma
Explanation:The patient’s symptoms are consistent with acute closed-angle glaucoma, which is an urgent ophthalmological emergency. They are experiencing a headache with unilateral eye pain, reduced vision, visual haloes, a red and congested eye with a cloudy cornea, and a dilated, unresponsive pupil. These symptoms may be triggered by darkness or dilating eye drops. Treatment should involve laying the patient flat to relieve angle pressure, administering pilocarpine eye drops to constrict the pupil, acetazolamide orally to reduce aqueous humour production, and providing analgesia. Referral to secondary care is necessary.
It is important to differentiate this condition from other potential causes of the patient’s symptoms. Central retinal vein occlusion, for example, would cause sudden painless loss of vision and severe retinal haemorrhages on fundoscopy. Migraines typically involve a visual or somatosensory aura followed by a unilateral throbbing headache, nausea, vomiting, and photophobia. Subarachnoid haemorrhages present with a sudden, severe headache, rather than a gradually worsening one accompanied by eye signs. Temporal arteritis may cause pain when chewing, difficulty brushing hair, and thickened temporal arteries visible on examination. However, the presence of a dilated, fixed pupil with conjunctival injection should steer the clinician away from a diagnosis of migraine.
Acute angle closure glaucoma (AACG) is a type of glaucoma where there is a rise in intraocular pressure (IOP) due to a blockage in the outflow of aqueous humor. This condition is more likely to occur in individuals with hypermetropia, pupillary dilation, and lens growth associated with aging. Symptoms of AACG include severe pain, decreased visual acuity, a hard and red eye, haloes around lights, and a semi-dilated non-reacting pupil. AACG is an emergency and requires urgent referral to an ophthalmologist. The initial medical treatment involves a combination of eye drops, such as a direct parasympathomimetic, a beta-blocker, and an alpha-2 agonist, as well as intravenous acetazolamide to reduce aqueous secretions. Definitive management involves laser peripheral iridotomy, which creates a tiny hole in the peripheral iris to allow aqueous humor to flow to the angle.
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This question is part of the following fields:
- Neurological System
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Question 23
Incorrect
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A 67-year-old man visits the clinic with a concern about a lump he has noticed at the corner of his jaw. Apart from this, he reports feeling well. During the examination, there is no visible swelling, but on palpation, you detect a hard, immovable mass located about 2 cm above the angle of the mandible. Based on your assessment, you suspect that the patient may have a parotid gland tumor. If this is the case, the tumor may cause additional symptoms if it affects the cranial nerve that passes through the parotid gland. Which cranial nerve has a path that runs through the substance of the parotid gland?
Your Answer:
Correct Answer: Facial nerve
Explanation:The parotid gland contains the facial nerve, which divides into five branches: the temporal, zygomatic, buccal, marginal mandibular, and cervical branches. The mandibular nerve, a division of the trigeminal nerve, carries both sensory and motor fibers, providing sensation to the lower lip, lower teeth and gums, chin, and jaw, and motor innervation to muscles involved in chewing and other functions. The glossopharyngeal nerve, the ninth cranial nerve, has various functions, including carrying taste and sensation from the back of the tongue, pharyngeal wall, tonsils, middle ear, external auditory canal, and auricle, as well as supplying the parotid gland with parasympathetic fibers. The maxillary nerve, another division of the trigeminal nerve, carries only sensory fibers, providing sensation to the lower eyelid and cheeks, upper teeth and gums, palate, nasal cavity, and certain paranasal sinuses. The hypoglossal nerve, the twelfth cranial nerve, supplies the intrinsic muscles of the tongue and most of the extrinsic muscles, except for the palatoglossus. A parotid tumor, which is usually benign, can cause symptoms such as a mass, tenderness of the gland, facial nerve palsy, or lymphatic infiltration.
The facial nerve is responsible for supplying the muscles of facial expression, the digastric muscle, and various glandular structures. It also contains a few afferent fibers that originate in the genicular ganglion and are involved in taste. Bilateral facial nerve palsy can be caused by conditions such as sarcoidosis, Guillain-Barre syndrome, Lyme disease, and bilateral acoustic neuromas. Unilateral facial nerve palsy can be caused by these conditions as well as lower motor neuron issues like Bell’s palsy and upper motor neuron issues like stroke.
The upper motor neuron lesion typically spares the upper face, specifically the forehead, while a lower motor neuron lesion affects all facial muscles. The facial nerve’s path includes the subarachnoid path, where it originates in the pons and passes through the petrous temporal bone into the internal auditory meatus with the vestibulocochlear nerve. The facial canal path passes superior to the vestibule of the inner ear and contains the geniculate ganglion at the medial aspect of the middle ear. The stylomastoid foramen is where the nerve passes through the tympanic cavity anteriorly and the mastoid antrum posteriorly, and it also includes the posterior auricular nerve and branch to the posterior belly of the digastric and stylohyoid muscle.
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This question is part of the following fields:
- Neurological System
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Question 24
Incorrect
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A 9-month-old baby is presented to the emergency department by their mother with recurrent seizures and an increasing head circumference. The infant has been experiencing excessive sleeping, vomiting, and irritability. An MRI scan of the brain reveals an enlarged posterior fossa and an absent cerebellar vermis. Which structure is anticipated to be in a raised position in this infant?
Your Answer:
Correct Answer: Tentorium cerebelli
Explanation:The Dandy-Walker malformation causes an enlargement of the posterior fossa, resulting in an accumulation of cerebrospinal fluid that pushes the tentorium cerebelli upwards. This can lead to symptoms due to the mass effect. The falx cerebri, pituitary gland, sphenoid sinus, and superior cerebellar peduncle are unlikely to be significantly affected by this condition.
The Three Layers of Meninges
The meninges are a group of membranes that cover the brain and spinal cord, providing support to the central nervous system and the blood vessels that supply it. These membranes can be divided into three distinct layers: the dura mater, arachnoid mater, and pia mater.
The outermost layer, the dura mater, is a thick fibrous double layer that is fused with the inner layer of the periosteum of the skull. It has four areas of infolding and is pierced by small areas of the underlying arachnoid to form structures called arachnoid granulations. The arachnoid mater forms a meshwork layer over the surface of the brain and spinal cord, containing both cerebrospinal fluid and vessels supplying the nervous system. The final layer, the pia mater, is a thin layer attached directly to the surface of the brain and spinal cord.
The meninges play a crucial role in protecting the brain and spinal cord from injury and disease. However, they can also be the site of serious medical conditions such as subdural and subarachnoid haemorrhages. Understanding the structure and function of the meninges is essential for diagnosing and treating these conditions.
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This question is part of the following fields:
- Neurological System
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Question 25
Incorrect
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A 21-year-old female is admitted with suspected meningitis. The House Officer is about to perform a lumbar puncture. What is the initial structure that the needle is likely to encounter upon insertion?
Your Answer:
Correct Answer: Supraspinous ligament
Explanation:Lumbar Puncture Procedure
Lumbar puncture is a medical procedure that involves obtaining cerebrospinal fluid. In adults, the procedure is typically performed at the L3/L4 or L4/5 interspace, which is located below the spinal cord’s termination at L1.
During the procedure, the needle passes through several layers. First, it penetrates the supraspinous ligament, which connects the tips of spinous processes. Then, it passes through the interspinous ligaments between adjacent borders of spinous processes. Next, the needle penetrates the ligamentum flavum, which may cause a give. Finally, the needle passes through the dura mater into the subarachnoid space, which is marked by a second give. At this point, clear cerebrospinal fluid should be obtained.
Overall, the lumbar puncture procedure is a complex process that requires careful attention to detail. By following the proper steps and guidelines, medical professionals can obtain cerebrospinal fluid safely and effectively.
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This question is part of the following fields:
- Neurological System
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Question 26
Incorrect
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A 42-year-old woman visits her doctor complaining of increased fatigue, especially towards the end of the day. Her husband notices visible signs of tiredness, with her eyes almost closed.
During the examination, the doctor observes a mass on the front of the neck and mild ptosis on both sides. To further investigate, the doctor instructs the patient to look down for a brief period and then return to primary gaze. Bilateral eyelid twitching is present upon returning to primary gaze.
What is the most commonly associated antibody with the probable diagnosis?Your Answer:
Correct Answer: Antibodies against acetylcholine receptors
Explanation:The patient’s symptoms and physical exam findings suggest a diagnosis of myasthenia gravis (MG). This autoimmune disorder affects the neuromuscular junction and can cause weakness and fatigue in the muscles. The presence of ptosis and diplopia, particularly worsening with prolonged use, is a common presentation in MG. Additionally, the presence of Cogan’s sign, twitching of the eyelids after a period of down-gazing, is a useful bedside test to assess for MG.
It is important to note that anti-smooth muscle antibodies, antibodies against voltage-gated calcium channels, and antimitochondrial antibodies are not associated with MG. These antibodies are instead associated with autoimmune hepatitis, Lambert Eaton myasthenic syndrome, and primary biliary cholangitis, respectively.
Myasthenia gravis is an autoimmune disorder that results in muscle weakness and fatigue, particularly in the eyes, face, neck, and limbs. It is more common in women and is associated with thymomas and other autoimmune disorders. Diagnosis is made through electromyography and testing for antibodies to acetylcholine receptors. Treatment includes acetylcholinesterase inhibitors and immunosuppression, and in severe cases, plasmapheresis or intravenous immunoglobulins may be necessary.
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This question is part of the following fields:
- Neurological System
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Question 27
Incorrect
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A 25-year-old man arrives at the emergency department after experiencing a 3-minute tonic-clonic seizure observed by his friend. He has had 2 similar episodes before. The neurology team evaluates him and starts him on carbamazepine.
What is the mechanism of action of carbamazepine in suppressing seizure activity?Your Answer:
Correct Answer: Inhibition of voltage-gated sodium channels
Explanation:The inhibition of Na channels and suppression of excitation are caused by sodium valproate and carbamazepine.
Treatment Options for Epilepsy
Epilepsy is a neurological disorder that affects millions of people worldwide. Treatment for epilepsy typically involves the use of antiepileptic drugs (AEDs) to control seizures. The decision to start AEDs is usually made after a second seizure, but there are certain circumstances where treatment may be initiated after the first seizure. These include the presence of a neurological deficit, structural abnormalities on brain imaging, unequivocal epileptic activity on EEG, or if the patient or their family considers the risk of having another seizure to be unacceptable.
It is important to note that there are specific drug treatments for different types of seizures. For generalized tonic-clonic seizures, males are typically prescribed sodium valproate, while females may be given lamotrigine or levetiracetam. For focal seizures, first-line treatment options include lamotrigine or levetiracetam, with carbamazepine, oxcarbazepine, or zonisamide used as second-line options. Ethosuximide is the first-line treatment for absence seizures, with sodium valproate or lamotrigine/levetiracetam used as second-line options. For myoclonic seizures, males are usually given sodium valproate, while females may be prescribed levetiracetam. Finally, for tonic or atonic seizures, males are typically given sodium valproate, while females may be prescribed lamotrigine.
It is important to work closely with a healthcare provider to determine the best treatment plan for each individual with epilepsy. Additionally, it is important to be aware of potential risks associated with certain AEDs, such as the use of sodium valproate during pregnancy, which has been linked to neurodevelopmental delays in children.
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This question is part of the following fields:
- Neurological System
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Question 28
Incorrect
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A 65-year-old man with amyotrophic lateral sclerosis visits his primary care physician complaining of difficulty swallowing and regurgitation. During the examination, the patient's uvula is observed to deviate to the left side of the mouth. The tongue remains unaffected, and taste perception is normal. No other abnormalities are detected upon examination of the oral cavity. Based on these findings, where is the lesion most likely located?
Your Answer:
Correct Answer: Left vagus nerve
Explanation:The uvula deviating away from the side of the lesion indicates a problem with the left vagus nerve, as this nerve controls the muscles of the soft palate and can cause uvula deviation when damaged. In cases of vagus nerve lesions, the uvula deviates in the opposite direction of the lesion. As the patient’s uvula deviates towards the right, the underlying issue must be with the left vagus nerve.
The left hypoglossal nerve cannot be the cause of the uvula deviation, as this nerve only provides motor innervation to the tongue muscles and cannot affect the uvula.
Similarly, the right hypoglossal nerve and right trigeminal nerve cannot cause uvula deviation, as they do not have any control over the uvula. Trigeminal nerve lesions may cause different clinical signs depending on the location of the lesion, such as masseteric wasting in the case of mandibular nerve damage.
Cranial nerves are a set of 12 nerves that emerge from the brain and control various functions of the head and neck. Each nerve has a specific function, such as smell, sight, eye movement, facial sensation, and tongue movement. Some nerves are sensory, some are motor, and some are both. A useful mnemonic to remember the order of the nerves is Some Say Marry Money But My Brother Says Big Brains Matter Most, with S representing sensory, M representing motor, and B representing both.
In addition to their specific functions, cranial nerves also play a role in various reflexes. These reflexes involve an afferent limb, which carries sensory information to the brain, and an efferent limb, which carries motor information from the brain to the muscles. Examples of cranial nerve reflexes include the corneal reflex, jaw jerk, gag reflex, carotid sinus reflex, pupillary light reflex, and lacrimation reflex. Understanding the functions and reflexes of the cranial nerves is important in diagnosing and treating neurological disorders.
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This question is part of the following fields:
- Neurological System
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Question 29
Incorrect
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A 23-year-old man is in a physical altercation and suffers a cut on the back of his wrist. Upon examination in the ER, it is discovered that the laceration runs horizontally over the area of the extensor retinaculum, which remains undamaged. Which of the following structures is the least probable to have been harmed in this situation?
Your Answer:
Correct Answer: Tendon of extensor indicis
Explanation:The extensor retinaculum starts its attachment to the radius near the styloid and then moves diagonally and downwards to wrap around the ulnar styloid without attaching to it. As a result, the extensor tendons are situated beneath the extensor retinaculum and are less prone to injury compared to the superficial structures.
The Extensor Retinaculum and its Related Structures
The extensor retinaculum is a thick layer of deep fascia that runs across the back of the wrist, holding the long extensor tendons in place. It attaches to the pisiform and triquetral bones medially and the end of the radius laterally. The retinaculum has six compartments that contain the extensor muscle tendons, each with its own synovial sheath.
Several structures are related to the extensor retinaculum. Superficial to the retinaculum are the basilic and cephalic veins, the dorsal cutaneous branch of the ulnar nerve, and the superficial branch of the radial nerve. Deep to the retinaculum are the tendons of the extensor carpi ulnaris, extensor digiti minimi, extensor digitorum, extensor indicis, extensor pollicis longus, extensor carpi radialis longus, extensor carpi radialis brevis, abductor pollicis longus, and extensor pollicis brevis.
The radial artery also passes between the lateral collateral ligament of the wrist joint and the tendons of the abductor pollicis longus and extensor pollicis brevis. Understanding the topography of these structures is important for diagnosing and treating wrist injuries and conditions.
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This question is part of the following fields:
- Neurological System
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Question 30
Incorrect
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A 16-year-old girl presents with a gradual weakness and muscle wasting of her left hand over the last 4 years. She has been a competitive long-distance runner for the past 5 years.
Upon neurological examination, there is significant atrophy and weakness of all intrinsic muscles, particularly the thenar muscles in the left hand. Sensation is reduced along the ulnar aspect of the hand and forearm. There are no tender areas or swelling over the shoulder joint, and shoulder movement is unimpeded.
A chest x-ray reveals the presence of cervical ribs on both sides.
What is the most probable diagnosis?Your Answer:
Correct Answer: Neurogenic thoracic outlet syndrome
Explanation:Thoracic outlet syndrome (TOS) is a condition where the brachial plexus, subclavian artery or vein is compressed at the thoracic outlet. One possible cause of TOS is the presence of a cervical rib, an extra rib that grows from the cervical spine. This can increase the risk of nerve or blood vessel compression, especially in individuals who engage in repetitive swimming activities.
Erb’s palsy, also known as Erb-Duchenne palsy, is a type of obstetric brachial plexus palsy that occurs when the upper brachial plexus is injured during birth. This can result in the loss of shoulder lateral rotators, arm flexors, and hand extensor muscles, leading to the characteristic Waiter’s tip deformity.
Klumpke paralysis is a neuropathy of the lower brachial plexus that can occur during a difficult delivery. It is typically caused by hyper-abduction traction and can result in a claw hand presentation, where the wrist and fingers are flexed and the forearm is supinated.
Carpal tunnel syndrome is a condition where the median nerve is compressed as it passes through the wrist, leading to numbness, tingling, burning, and pain in the thumb and fingers. However, this patient’s symptoms of reduced sensation along the ulnar aspect of the hand and forearm are not consistent with carpal tunnel syndrome.
Understanding Thoracic Outlet Syndrome
Thoracic outlet syndrome (TOS) is a condition that occurs when there is compression of the brachial plexus, subclavian artery, or vein at the thoracic outlet. This disorder can be either neurogenic or vascular, with the former accounting for 90% of cases. TOS is more common in young, thin women with long necks and drooping shoulders, and peak onset typically occurs in the fourth decade of life. The lack of widely agreed diagnostic criteria makes it difficult to determine the exact epidemiology of TOS.
TOS can develop due to neck trauma in individuals with anatomical predispositions. Anatomical anomalies can be in the form of soft tissue or osseous structures, with cervical rib being a well-known osseous anomaly. Soft tissue causes include scalene muscle hypertrophy and anomalous bands. Patients with TOS typically have a history of neck trauma preceding the onset of symptoms.
The clinical presentation of neurogenic TOS includes painless muscle wasting of hand muscles, hand weakness, and sensory symptoms such as numbness and tingling. If autonomic nerves are involved, patients may experience cold hands, blanching, or swelling. Vascular TOS, on the other hand, can lead to painful diffuse arm swelling with distended veins or painful arm claudication and, in severe cases, ulceration and gangrene.
To diagnose TOS, a neurological and musculoskeletal examination is necessary, and stress maneuvers such as Adson’s maneuvers may be attempted. Imaging modalities such as chest and cervical spine plain radiographs, CT or MRI, venography, or angiography may also be helpful. Treatment options for TOS include conservative management with education, rehabilitation, physiotherapy, or taping as the first-line management for neurogenic TOS. Surgical decompression may be warranted where conservative management has failed, especially if there is a physical anomaly. In vascular TOS, surgical treatment may be preferred, and other therapies such as botox injection are being investigated.
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This question is part of the following fields:
- Neurological System
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