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Question 1
Correct
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A 45-year-old female presents to the emergency department with severe back pain and no medical history except for a penicillin allergy. Following an MRI, she is diagnosed with osteomyelitis and prescribed a 6-week course of two antibiotics. However, a few days into treatment, she reports abdominal pain and diarrhea. Stool samples reveal the presence of Clostridium difficile toxins, leading to a diagnosis of pseudomembranous colitis. Which antibiotic is the most likely culprit for causing the C. difficile colitis?
Your Answer: Clindamycin
Explanation:The use of clindamycin as a treatment is linked to a significant risk of developing C. difficile infection. This antibiotic is commonly associated with Clostridium difficile colitis. Doxycycline has the potential to cause sensitivity to sunlight and birth defects, while trimethoprim can lead to high levels of potassium in the blood and is also harmful to developing fetuses. Vancomycin, on the other hand, can cause red man syndrome and is among the medications used to treat Clostridium difficile colitis.
Clostridium difficile is a type of bacteria that is commonly found in hospitals. It produces a toxin that can damage the intestines and cause a condition called pseudomembranous colitis. This bacteria usually develops when the normal gut flora is disrupted by broad-spectrum antibiotics, with second and third generation cephalosporins being the leading cause. Other risk factors include the use of proton pump inhibitors. Symptoms of C. difficile infection include diarrhea, abdominal pain, and a raised white blood cell count. The severity of the infection can be determined using the Public Health England severity scale.
To diagnose C. difficile infection, a stool sample is tested for the presence of the C. difficile toxin. Treatment involves reviewing current antibiotic therapy and stopping antibiotics if possible. For a first episode of infection, oral vancomycin is the first-line therapy for 10 days, followed by oral fidaxomicin as second-line therapy and oral vancomycin with or without IV metronidazole as third-line therapy. Recurrent infections may require different treatment options, such as oral fidaxomicin within 12 weeks of symptom resolution or oral vancomycin or fidaxomicin after 12 weeks of symptom resolution. In life-threatening cases, oral vancomycin and IV metronidazole may be used, and surgery may be considered with specialist advice. Other therapies, such as bezlotoxumab and fecal microbiota transplant, may also be considered for preventing recurrences in certain cases.
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This question is part of the following fields:
- Gastrointestinal System
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Question 2
Correct
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A 27-year-old man is involved in a car crash resulting in a fracture of his right tibia. He undergoes fasciotomies and an external fixator is applied. Within 48 hours, his serum creatinine levels increase and his urine is analyzed, revealing the presence of muddy brown casts. What is the probable underlying diagnosis?
Your Answer: Acute tubular necrosis
Explanation:It is probable that the patient suffered from compartment syndrome due to a tibial fracture and subsequent fasciotomies, which can result in myoglobinuria. The combination of deteriorating kidney function and the presence of muddy brown casts in the urine strongly indicate acute tubular necrosis. Acute interstitial nephritis is typically caused by drug toxicity and does not typically lead to the presence of muddy brown casts in the urine.
Understanding the Difference between Acute Tubular Necrosis and Prerenal Uraemia
Acute kidney injury can be caused by various factors, including prerenal uraemia and acute tubular necrosis. It is important to differentiate between the two to determine the appropriate treatment. Prerenal uraemia occurs when the kidneys hold on to sodium to preserve volume, leading to decreased blood flow to the kidneys. On the other hand, acute tubular necrosis is caused by damage to the kidney tubules, which can be due to various factors such as toxins, infections, or ischemia.
To differentiate between the two, several factors can be considered. In prerenal uraemia, the urine sodium level is typically less than 20 mmol/L, while in acute tubular necrosis, it is usually greater than 40 mmol/L. The urine osmolality is also higher in prerenal uraemia, typically above 500 mOsm/kg, while in acute tubular necrosis, it is usually below 350 mOsm/kg. The fractional sodium excretion is less than 1% in prerenal uraemia, while it is greater than 1% in acute tubular necrosis. Additionally, the response to fluid challenge is typically good in prerenal uraemia, while it is poor in acute tubular necrosis.
Other factors that can help differentiate between the two include the serum urea:creatinine ratio, fractional urea excretion, urine:plasma osmolality, urine:plasma urea, specific gravity, and urine sediment. By considering these factors, healthcare professionals can accurately diagnose and treat acute kidney injury.
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This question is part of the following fields:
- Renal System
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Question 3
Incorrect
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A 23-year-old male visits his GP complaining of polyuria, chronic thirst and pale-coloured urine that have persisted for 3 months. He had a concussion from a car accident a month before the onset of his urinary symptoms. The patient is diagnosed with cranial diabetes insipidus after undergoing several tests.
What would the water deprivation test likely reveal in this case?Your Answer: High urine osmolality after fluid deprivation, but normal after desmopressin
Correct Answer: Low urine osmolality after fluid deprivation, but high after desmopressin
Explanation:The correct answer is low urine osmolality after fluid deprivation, but high after desmopressin, for a patient with cranial diabetes insipidus (DI). This condition is characterized by polyuria, chronic thirst, and pale-coloured urine, and is caused by insufficient antidiuretic hormone (ADH) secretion. As a result, the kidneys are unable to concentrate urine, leading to a low urine osmolality even during water deprivation. However, the kidneys will respond to desmopressin (synthetic ADH) to produce concentrated urine.
High urine osmolality after both fluid deprivation and desmopressin is incorrect, as it would be seen in a healthy individual or a patient with primary polydipsia, a psychogenic disorder characterized by excessive drinking despite being properly hydrated.
Low urine osmolality after both fluid deprivation and desmopressin is incorrect, as this is typical of nephrogenic DI, a condition in which the kidneys are insensitive to ADH.
High urine osmolality after fluid deprivation, but normal after desmopressin is incorrect, as this would not be commonly seen with any pathological state.
Low urine osmolality after desmopressin, but high after fluid deprivation is incorrect, as this would not be commonly seen with any pathological state.
The water deprivation test is a diagnostic tool used to assess patients with polydipsia, or excessive thirst. During the test, the patient is instructed to refrain from drinking water, and their bladder is emptied. Hourly measurements of urine and plasma osmolalities are taken to monitor changes in the body’s fluid balance. The results of the test can help identify the underlying cause of the patient’s polydipsia. Normal results show a high urine osmolality after the administration of DDAVP, while psychogenic polydipsia is characterized by a low urine osmolality. Cranial DI and nephrogenic DI are both associated with high plasma osmolalities and low urine osmolalities.
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This question is part of the following fields:
- Endocrine System
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Question 4
Correct
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You have been asked to review a 63-year-old man on the medical ward who was recently treated for an exacerbation of pulmonary oedema. His past medical history includes heart failure. He is currently on a course of antibiotics for prostatitis.
His blood results from yesterday are shown below:
Na+ 141 mmol/l
K+ 4.3 mmol/l
Urea 6 mmol/l
Creatinine 60 µmol/l
His blood results from today are shown below:
Na+ 140 mmol/l
K+ 4.6 mmol/l
Urea 15 mmol/l
Creatinine 180 µmol/l
What is the most probable reason for the change in kidney function?Your Answer: Concomitant use of furosemide and gentamicin resulting in renal failure
Explanation:The risk of renal failure increases when furosemide and gentamicin are used together. Furosemide is the primary diuretic for treating acute pulmonary edema, but its concurrent use with gentamicin can lead to kidney failure. The patient’s blood test results indicate acute kidney injury, which is likely caused by gentamicin toxicity.
Acute kidney injury can result from pre-renal causes such as sepsis and dehydration, and in such cases, the blood test would show a significant increase in urea levels disproportionate to the rise in creatinine.
Bendroflumethiazide is not a commonly used medication for managing acute pulmonary edema.
Metronidazole is not significantly associated with nephrotoxicity.
Gentamicin is a type of antibiotic known as an aminoglycoside. It is not easily dissolved in lipids, so it is typically administered through injection or topical application. It is commonly used to treat infections such as infective endocarditis and otitis externa. However, gentamicin can have adverse effects on the body, such as ototoxicity, which can cause damage to the auditory or vestibular nerves. This damage is irreversible. Gentamicin can also cause nephrotoxicity, which can lead to acute tubular necrosis. The risk of toxicity increases when gentamicin is used in conjunction with furosemide. Lower doses and more frequent monitoring are necessary to prevent these adverse effects. Gentamicin is contraindicated in patients with myasthenia gravis. To ensure safe dosing, plasma concentrations of gentamicin are monitored. Peak levels are measured one hour after administration, and trough levels are measured just before the next dose. If the trough level is high, the interval between doses should be increased. If the peak level is high, the dose should be decreased.
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This question is part of the following fields:
- General Principles
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Question 5
Correct
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A 6-year-old girl arrives at the Emergency Department complaining of a headache, neck stiffness and sensitivity to light. She is diagnosed with meningitis and given IV cefuroxime. What is the mechanism of action of this antibiotic?
Your Answer: Inhibits cell wall formation
Explanation:Cefuroxime belongs to the cephalosporin group of antibiotics that hinder the formation of cell walls.
Metronidazole acts by causing direct damage to DNA.
Quinolones, like ciprofloxacin, function by preventing DNA synthesis.
Rifampicin works by inhibiting RNA synthesis.
Trimethoprim and sulphonamides work by blocking the formation of folic acid.
Antibiotics work in different ways to kill or inhibit the growth of bacteria. The commonly used antibiotics can be classified based on their gross mechanism of action. The first group inhibits cell wall formation by either preventing peptidoglycan cross-linking (penicillins, cephalosporins, carbapenems) or peptidoglycan synthesis (glycopeptides like vancomycin). The second group inhibits protein synthesis by acting on either the 50S subunit (macrolides, chloramphenicol, clindamycin, linezolid, streptogrammins) or the 30S subunit (aminoglycosides, tetracyclines) of the bacterial ribosome. The third group inhibits DNA synthesis (quinolones like ciprofloxacin) or damages DNA (metronidazole). The fourth group inhibits folic acid formation (sulphonamides and trimethoprim), while the fifth group inhibits RNA synthesis (rifampicin). Understanding the mechanism of action of antibiotics is important in selecting the appropriate drug for a particular bacterial infection.
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This question is part of the following fields:
- General Principles
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Question 6
Incorrect
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A 35-year-old patient with consistent PR bleeding is diagnosed with Crohn's disease. What is the primary medication used to induce remission of this condition?
Your Answer: Azathioprine
Correct Answer: Prednisolone
Explanation:To induce remission of Crohn’s disease, glucocorticoids (whether oral, topical or intravenous) are typically the first line of treatment. 5-ASA drugs are considered a second option for inducing remission of IBD. Azathioprine is more commonly used for maintaining remission. Steroids are specifically used to induce remission of Crohn’s disease. Infliximab is particularly effective for treating refractory disease and fistulating Crohn’s.
Crohn’s disease is a type of inflammatory bowel disease that can affect any part of the digestive tract. The National Institute for Health and Care Excellence (NICE) has published guidelines for managing this condition. Patients are advised to quit smoking, as it can worsen Crohn’s disease. While some studies suggest that NSAIDs and the combined oral contraceptive pill may increase the risk of relapse, the evidence is not conclusive.
To induce remission, glucocorticoids are typically used, but budesonide may be an alternative for some patients. Enteral feeding with an elemental diet may also be used, especially in young children or when there are concerns about steroid side effects. Second-line options include 5-ASA drugs, such as mesalazine, and add-on medications like azathioprine or mercaptopurine. Infliximab is useful for refractory disease and fistulating Crohn’s, and metronidazole is often used for isolated peri-anal disease.
Maintaining remission involves stopping smoking and using azathioprine or mercaptopurine as first-line options. Methotrexate is a second-line option. Surgery is eventually required for around 80% of patients with Crohn’s disease, depending on the location and severity of the disease. Complications of Crohn’s disease include small bowel cancer, colorectal cancer, and osteoporosis. Before offering azathioprine or mercaptopurine, it is important to assess thiopurine methyltransferase (TPMT) activity.
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This question is part of the following fields:
- Gastrointestinal System
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Question 7
Correct
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A 48-year-old woman presents to the clinic with complaints of abdominal pain and constipation. During the examination, you observe blue lines on the gum margin. She also reports experiencing weakness in her legs over the past few days. What is the probable diagnosis?
Your Answer: Lead poisoning
Explanation:Lead poisoning is a condition that should be considered when a patient presents with abdominal pain and neurological symptoms, along with acute intermittent porphyria. This condition is caused by defective ferrochelatase and ALA dehydratase function. Symptoms of lead poisoning include abdominal pain, peripheral neuropathy (mainly motor), neuropsychiatric features, fatigue, constipation, and blue lines on the gum margin (which is rare in children and only present in 20% of adult patients).
To diagnose lead poisoning, doctors typically measure the patient’s blood lead level, with levels greater than 10 mcg/dl considered significant. A full blood count may also be performed, which can reveal microcytic anemia and red cell abnormalities such as basophilic stippling and clover-leaf morphology. Additionally, raised serum and urine levels of delta aminolaevulinic acid may be seen, which can sometimes make it difficult to differentiate from acute intermittent porphyria. Urinary coproporphyrin is also increased, while urinary porphobilinogen and uroporphyrin levels are normal to slightly increased. In children, lead can accumulate in the metaphysis of the bones, although x-rays are not typically part of the standard work-up.
Various chelating agents are currently used to manage lead poisoning, including dimercaptosuccinic acid (DMSA), D-penicillamine, EDTA, and dimercaprol. These agents work to remove the lead from the body and can help alleviate symptoms.
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This question is part of the following fields:
- Haematology And Oncology
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Question 8
Incorrect
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A couple brings in their adolescent son who has been diagnosed with haemophilia A. The parents are both adoptees and have no knowledge of their biological families. Given this information, what is the most probable mode of inheritance for their son's condition?
Your Answer: Both of his parents are likely carriers for haemophilia A
Correct Answer: His mother is a carrier for haemophilia A
Explanation:It is more probable that the condition is inherited rather than acquired through spontaneous mutations.
X-linked recessive inheritance affects only males, except in cases of Turner’s syndrome where females are affected due to having only one X chromosome. This type of inheritance is transmitted by carrier females, and male-to-male transmission is not observed. Affected males can only have unaffected sons and carrier daughters.
If a female carrier has children, each male child has a 50% chance of being affected, while each female child has a 50% chance of being a carrier. It is rare for an affected father to have children with a heterozygous female carrier, but in some Afro-Caribbean communities, G6PD deficiency is relatively common, and homozygous females with clinical manifestations of the enzyme defect can be seen.
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This question is part of the following fields:
- General Principles
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Question 9
Incorrect
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A 10-year-old girl with a peanut allergy ingests a candy bar containing nuts and experiences difficulty breathing. Her mother quickly administers an IM injection to her lateral thigh, resulting in rapid improvement. What is the mechanism of action of the drug used in the injection?
Your Answer: Via ligand-gated ion channels
Correct Answer: Via G protein-coupled receptors
Explanation:Adrenaline exerts its effects by binding to a G protein-coupled receptor located on the cell membrane. Other types of membrane receptors include ligand-gated ion channels and tyrosine kinase receptors. In contrast, steroid hormones bind to intranuclear receptors and modulate DNA transcription. Second messengers such as inositol triphosphate (IP3) bind to cytoplasmic or intracellular receptors.
Membrane receptors are proteins located on the surface of cells that receive signals from outside the cell and transmit them inside. There are four main types of membrane receptors: ligand-gated ion channel receptors, tyrosine kinase receptors, guanylate cyclase receptors, and G protein-coupled receptors. Ligand-gated ion channel receptors mediate fast responses and include nicotinic acetylcholine, GABA-A & GABA-C, and glutamate receptors. Tyrosine kinase receptors include receptor tyrosine kinase such as insulin, insulin-like growth factor (IGF), and epidermal growth factor (EGF), and non-receptor tyrosine kinase such as PIGG(L)ET, which stands for Prolactin, Immunomodulators (cytokines IL-2, Il-6, IFN), GH, G-CSF, Erythropoietin, and Thrombopoietin.
Guanylate cyclase receptors contain intrinsic enzyme activity and include atrial natriuretic factor and brain natriuretic peptide. G protein-coupled receptors generally mediate slow transmission and affect metabolic processes. They are activated by a wide variety of extracellular signals such as peptide hormones, biogenic amines (e.g. adrenaline), lipophilic hormones, and light. These receptors have 7-helix membrane-spanning domains and consist of 3 main subunits: alpha, beta, and gamma. The alpha subunit is linked to GDP. Ligand binding causes conformational changes to the receptor, GDP is phosphorylated to GTP, and the alpha subunit is activated. G proteins are named according to the alpha subunit (Gs, Gi, Gq).
The mechanism of G protein-coupled receptors varies depending on the type of G protein involved. Gs stimulates adenylate cyclase, which increases cAMP and activates protein kinase A. Gi inhibits adenylate cyclase, which decreases cAMP and inhibits protein kinase A. Gq activates phospholipase C, which splits PIP2 to IP3 and DAG and activates protein kinase C. Examples of G protein-coupled receptors include beta-1 receptors (epinephrine, norepinephrine, dobutamine), beta-2 receptors (epinephrine, salbuterol), H2 receptors (histamine), D1 receptors (dopamine), V2 receptors (vas
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This question is part of the following fields:
- General Principles
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Question 10
Correct
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What is the cause of the symptoms of weakness, dermatitis, diarrhoea and dementia in pellagra?
Your Answer: Deficiency of the vitamin niacin
Explanation:Niacin Deficiency and Other Genetic Diseases
Niacin, a vitamin present in two forms – nicotinamide and nicotinic acid, is found in a variety of plant and animal foodstuffs. However, in some cases, the form of the vitamin is not easily absorbed by the human body, leading to deficiency. This deficiency is common in areas where maize is the primary dietary carbohydrate. Additionally, niacin can be produced by the body from the amino acid tryptophan. Diseases that affect the availability of tryptophan, such as Hartnup disease and carcinoid syndrome, can also result in niacin deficiency.
Pellagra is a condition that arises from niacin deficiency. It initially presents with non-specific symptoms such as nausea, fatigue, and reduced appetite, followed by pigmented dermatitis in sun-exposed areas, gastrointestinal disturbance, mood disturbance, and dementia in severe cases.
Apart from niacin deficiency, genetic diseases affecting collagen synthesis, such as Ehlers Danlos, present with symptoms of fragile stretchy skin and joint hypermobility. Genetic diseases affecting haemoglobin, such as sickle cell anaemia, present with symptoms of pain, hepatosplenomegaly, shortness of breath, and anaemia. Deficiencies in B12 and folate can also lead to macrocytic anaemia, paresthesia, and lethargy.
In conclusion, the causes and symptoms of niacin deficiency and other genetic diseases is crucial for early diagnosis and effective treatment. A balanced diet and regular medical check-ups can help prevent and manage these conditions.
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This question is part of the following fields:
- Basic Sciences
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Question 11
Incorrect
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A 25-year-old male has come to the clinic complaining of a low-grade fever and a small, painless lesion on his penis that is red and raw. He also has inguinal lymphadenopathy. He admits to having unprotected vaginal sex while on vacation four weeks ago. What is the probable diagnosis?
Your Answer: Herpes simplex virus
Correct Answer: Primary syphilis
Explanation:Syphilis and its Symptoms
Syphilis is a sexually transmitted infection caused by Treponema pallidum. The primary stage of syphilis is characterized by a painless chancre that appears three to six weeks after contact. This ulcer is highly infectious and continuously sheds motile spirochetes. After six weeks, the lesion may resolve, leading the patient to believe they are cured. However, without treatment, the spirochaete remains in the body and can lead to secondary syphilis.
It is important to note that painful genital ulcers are typically caused by herpes simplex virus and H. ducreyi, while painless ulcers are caused by T. pallidum and Chlamydia trachomatis. HPV, on the other hand, typically causes genital warts, with strains six and 11 causing warts and strains 16 and 18 being associated with cervical cancer.
Secondary syphilis is a disseminated disease that can cause a maculopapular rash, which may involve the palms and soles. This rash is known as keratoderma blennorrhagicum (KB) and can sometimes present in patients with reactive arthritis. Additionally, patients with secondary syphilis may present with condylomata lata, which are white fleshy lesions on the genitals and signify the most infectious stage.
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This question is part of the following fields:
- Infectious Diseases
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Question 12
Correct
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During a block dissection of the thigh, the sartorius muscle is identified. What is the nerve supply to this muscle?
Your Answer: Anterior division of the femoral nerve
Explanation:The superficial femoral nerve primarily provides cutaneous branches, but it also innervates the sartorius muscle.
The Sartorius Muscle: Anatomy and Function
The sartorius muscle is the longest strap muscle in the human body and is located in the anterior compartment of the thigh. It is the most superficial muscle in this region and has a unique origin and insertion. The muscle originates from the anterior superior iliac spine and inserts on the medial surface of the body of the tibia, anterior to the gracilis and semitendinosus muscles. The sartorius muscle is innervated by the femoral nerve (L2,3).
The primary action of the sartorius muscle is to flex the hip and knee, while also slightly abducting the thigh and rotating it laterally. It also assists with medial rotation of the tibia on the femur, which is important for movements such as crossing one leg over the other. The middle third of the muscle, along with its strong underlying fascia, forms the roof of the adductor canal. This canal contains important structures such as the femoral vessels, the saphenous nerve, and the nerve to vastus medialis.
In summary, the sartorius muscle is a unique muscle in the anterior compartment of the thigh that plays an important role in hip and knee flexion, thigh abduction, and lateral rotation. Its location and relationship to the adductor canal make it an important landmark for surgical procedures in the thigh region.
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This question is part of the following fields:
- Musculoskeletal System And Skin
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Question 13
Correct
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A 78-year-old man visits your clinic with a chief complaint of shoulder weakness. He reports that his left shoulder has been weak for the past 5 months and the weakness has been gradually worsening. Upon examination, you observe atrophy of the trapezius muscle. When you ask him to shrug his shoulders, you notice weakness on his left side. You suspect that the patient's presentation is caused by a lesion affecting the accessory nerve. Which other muscle is innervated by the accessory nerve?
Your Answer: Sternocleidomastoid
Explanation:The sternocleidomastoid muscle is the correct answer. It originates from two points – the upper part of the sternum’s manubrium and the medial clavicle. It runs diagonally across the neck and attaches to the mastoid process of the temporal bone and the lateral area of the superior nuchal line. The accessory nerve and primary rami of C2-3 provide innervation to this muscle.
Both the deltoid and teres minor muscles are innervated by the axillary nerve.
The pectoralis major muscle is innervated by the medial and lateral pectoral nerves, which are both branches of the brachial plexus.
The Accessory Nerve and Its Functions
The accessory nerve is the eleventh cranial nerve that provides motor innervation to the sternocleidomastoid and trapezius muscles. It is important to examine the function of this nerve by checking for any loss of muscle bulk in the shoulders, asking the patient to shrug their shoulders against resistance, and turning their head against resistance.
Iatrogenic injury, which is caused by medical treatment or procedures, is a common cause of isolated accessory nerve lesions. This is especially true for surgeries in the posterior cervical triangle, such as lymph node biopsy. It is important to be aware of the potential for injury to the accessory nerve during these procedures to prevent any long-term complications.
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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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What is the initial event that triggers puberty in girls?
Your Answer: Sudden increase in oestrogen production
Correct Answer: Nocturnal rise in luteinising hormone (LH)
Explanation:Puberty is triggered by endocrine changes that begin years before visible changes occur. The initial event is an increase in nocturnal LH secretion under the stimulation of GnRH. LH patterns of secretion change over time, resembling the adult pattern. In females, increased secretion of GnRH, LH, FSH, and estrogen causes the development of secondary sexual characteristics, adrenarche, gonadarche, thelarche, and menarche. The growth spurt for girls occurs in mid-puberty around the age of 12.
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This question is part of the following fields:
- Paediatrics
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Question 15
Correct
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A 72-year-old man presents to the emergency department following a fall on his outstretched arm. He has a medical history of osteoporosis and takes calcium, vitamin D, and alendronic acid.
During the examination, he experiences tenderness at the proximal humerus and is unable to abduct his shoulder. However, his elbow, wrist, and hand appear normal.
After a plain radiography, it is discovered that he has a fracture of the proximal humerus. Which nerve has been affected by this injury?Your Answer: Axillary nerve
Explanation:The correct nerve associated with loss of shoulder abduction due to denervation of the deltoid muscle in an elderly man with a proximal humerus fracture is the axillary nerve (C5,C6). Injury to the long thoracic, musculocutaneous, radial, and ulnar nerves are less likely based on the mechanism of injury and examination findings.
Upper limb anatomy is a common topic in examinations, and it is important to know certain facts about the nerves and muscles involved. The musculocutaneous nerve is responsible for elbow flexion and supination, and typically only injured as part of a brachial plexus injury. The axillary nerve controls shoulder abduction and can be damaged in cases of humeral neck fracture or dislocation, resulting in a flattened deltoid. The radial nerve is responsible for extension in the forearm, wrist, fingers, and thumb, and can be damaged in cases of humeral midshaft fracture, resulting in wrist drop. The median nerve controls the LOAF muscles and can be damaged in cases of carpal tunnel syndrome or elbow injury. The ulnar nerve controls wrist flexion and can be damaged in cases of medial epicondyle fracture, resulting in a claw hand. The long thoracic nerve controls the serratus anterior and can be damaged during sports or as a complication of mastectomy, resulting in a winged scapula. The brachial plexus can also be damaged, resulting in Erb-Duchenne palsy or Klumpke injury, which can cause the arm to hang by the side and be internally rotated or associated with Horner’s syndrome, respectively.
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This question is part of the following fields:
- Musculoskeletal System And Skin
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Question 16
Correct
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As an investigator, you will be participating in a clinical trial of a new antihypertensive agent. The drug has already been tested on healthy volunteers, but this trial will be the first to involve patients. The aim of the trial is to determine the optimal dosage for therapy, which will be used in future studies. Are you ready to take part in this clinical trial?
Your Answer: Phase 2 study
Explanation:Phases of Clinical Trials
Clinical trials are conducted in several phases to determine the safety and efficacy of a new drug. The first phase, known as phase 1, involves testing the drug on healthy volunteers to determine its safety. In phase 2, the drug is tested on patients across a range of doses to establish the most effective dose with respect to clinical efficacy and adverse events. The third phase, known as phase 3, involves expanding the number of patients to confirm the drug’s efficacy and adverse event profile. This phase is conducted prior to registration. Finally, in phase 4, the drug is tested post-marketing to support clinical endpoints for reimbursement or to support marketing messages. These phases are crucial in determining the safety and efficacy of a new drug before it is made available to the public.
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This question is part of the following fields:
- Pharmacology
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Question 17
Correct
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Which of the following structures is situated between the lateral and medial heads of the triceps muscle?
Your Answer: Radial nerve
Explanation:The correct nerve that runs in its groove between the two heads is the radial nerve. The ulnar nerve is positioned anterior to the medial head, while the axillary nerve passes through the quadrangular space located above the lateral head of the triceps muscle. As a result, the lateral border of the quadrangular space is the humerus.
Anatomy of the Triceps Muscle
The triceps muscle is a large muscle located on the back of the upper arm. It is composed of three heads: the long head, lateral head, and medial head. The long head originates from the infraglenoid tubercle of the scapula, while the lateral head originates from the dorsal surface of the humerus, lateral and proximal to the groove of the radial nerve. The medial head originates from the posterior surface of the humerus on the inferomedial side of the radial groove and both of the intermuscular septae.
All three heads of the triceps muscle insert into the olecranon process of the ulna, with some fibers inserting into the deep fascia of the forearm and the posterior capsule of the elbow. The triceps muscle is innervated by the radial nerve and supplied with blood by the profunda brachii artery.
The primary action of the triceps muscle is elbow extension. The long head can also adduct the humerus and extend it from a flexed position. The radial nerve and profunda brachii vessels lie between the lateral and medial heads of the triceps muscle. Understanding the anatomy of the triceps muscle is important for proper diagnosis and treatment of injuries or conditions affecting this muscle.
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This question is part of the following fields:
- Musculoskeletal System And Skin
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Question 18
Incorrect
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A mother brings in her 8-month old child worried about her development. The baby has been having trouble with feeding and cannot sit without support. The mother is anxious because her first child was able to sit without support at 6 months. The child has a history of recurrent respiratory tract infections.
The doctor orders a series of blood tests to help identify potential causes.
After receiving the lab results, the doctor notes an abnormally high concentration of plasma lysosomal enzymes and positive inclusion bodies and peripheral blood lymphocytes.
What deficiency in enzymes is responsible for the symptoms seen in this child?Your Answer: Lysosomal acid alpha-glucosidase
Correct Answer: N-acetylglucosamine-1-phosphate transferase
Explanation:Inclusion-cell disease, also known as mucolipidosis II (ML II), is caused by a defect in the enzyme N-acetylglucosamine-1-phosphate transferase, which is located in the Golgi apparatus. This disease is classified as a lysosomal storage disease. Other conditions in this family and their associated enzyme defects include Hurler’s disease (alpha-L iduronidase), Pompe disease (lysosomal acid alpha-glucosidase), Tay-Sachs disease (Hexosaminidase A), and Fabry’s disease (alpha-galactosidase).
I-Cell Disease: A Lysosomal Storage Disease
The Golgi apparatus is responsible for modifying, sorting, and packaging molecules that are meant for cell secretion. However, a defect in N-acetylglucosamine-1-phosphate transferase can cause I-cell disease, also known as inclusion cell disease. This disease results in the failure of the Golgi apparatus to transfer phosphate to mannose residues on specific proteins.
I-cell disease is a type of lysosomal storage disease that can cause a range of clinical features. These include coarse facial features, which are similar to those seen in Hurler syndrome. Restricted joint movement, clouding of the cornea, and hepatosplenomegaly are also common symptoms. Despite its rarity, I-cell disease can have a significant impact on affected individuals and their families.
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This question is part of the following fields:
- General Principles
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Question 19
Correct
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A man in his 50s is diagnosed with pernicious anaemia. What is the probable cause for this condition?
Your Answer: Autoimmune antibodies to parietal cells
Explanation:The destruction of gastric parietal cells, often due to autoimmune factors, is a primary cause of pernicious anaemia. In some cases, mixed patterns may be present and further diagnostic assessment may be necessary, particularly in instances of bacterial overgrowth.
Pernicious anaemia is a condition that results in a deficiency of vitamin B12 due to an autoimmune disorder affecting the gastric mucosa. The term pernicious refers to the gradual and subtle harm caused by the condition, which often leads to delayed diagnosis. While pernicious anaemia is the most common cause of vitamin B12 deficiency, other causes include atrophic gastritis, gastrectomy, and malnutrition. The condition is characterized by the presence of antibodies to intrinsic factor and/or gastric parietal cells, which can lead to reduced vitamin B12 absorption and subsequent megaloblastic anaemia and neuropathy.
Pernicious anaemia is more common in middle to old age females and is associated with other autoimmune disorders such as thyroid disease, type 1 diabetes mellitus, Addison’s, rheumatoid, and vitiligo. Symptoms of the condition include anaemia, lethargy, pallor, dyspnoea, peripheral neuropathy, subacute combined degeneration of the spinal cord, neuropsychiatric features, mild jaundice, and glossitis. Diagnosis is made through a full blood count, vitamin B12 and folate levels, and the presence of antibodies.
Management of pernicious anaemia involves vitamin B12 replacement, usually given intramuscularly. Patients with neurological features may require more frequent doses. Folic acid supplementation may also be necessary. Complications of the condition include an increased risk of gastric cancer.
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This question is part of the following fields:
- Gastrointestinal System
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Question 20
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What is the antibiotic that cannot be absorbed orally, but can be effective in treating antibiotic-induced diarrhea?
Your Answer: Vancomycin
Explanation:Antibiotic-Associated Diarrhoea and Clostridium Difficile Infection
The majority of cases of antibiotic-associated diarrhoea are non-infective and are caused by changes in the normal gut flora. However, in certain patients, the use of broad-spectrum antibiotics can lead to the development of Clostridium difficile infection. This Gram-positive bacillus causes a colitis that results in profuse watery diarrhoea. In severe cases, the entire colonic mucosa is affected, leading to the formation of a pseudomembrane and severe dilatation of the colon, which can be life-threatening.
C. difficile is first-line treated with metronidazole, but if this is ineffective, oral vancomycin is used as a second-line treatment. Vancomycin is a glycopeptide antibiotic that has zero oral bioavailability, meaning that if it is given orally, none of it will enter the bloodstream. This makes it an ideal treatment for infections that are limited to the gastrointestinal tract, but it would not be useful for treating a systemic infection.
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This question is part of the following fields:
- Microbiology
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