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  • Question 1 - A 15-year-old student presents with low back pain that radiates to the back...

    Correct

    • A 15-year-old student presents with low back pain that radiates to the back of their legs. They have an elevated ESR and negative serum rheumatoid factor. A spine radiograph reveals anterior squaring of the vertebrae.
      What is the most probable diagnosis?

      Your Answer: Ankylosing spondylitis (AS)

      Explanation:

      Ankylosing spondylitis (AS) is a type of arthritis that is characterized by morning stiffness lasting more than 30 minutes, improvement of back pain with exercise but not rest, awakening due to back pain during the second half of the night, and alternating buttock pain. It is a seronegative spondyloarthropathy, meaning that the rheumatoid factor will be negative. Radiographically, sacroiliitis is often the first abnormality seen. ESR and CRP are usually raised, and HLA-B27 testing may provide supporting evidence. Lumbar disc prolapse with sciatica, rheumatoid arthritis, spinal stenosis, and Paget’s disease of bone are other conditions that may cause similar symptoms but have different characteristics and diagnostic criteria.

    • This question is part of the following fields:

      • Musculoskeletal
      731.5
      Seconds
  • Question 2 - A 35-year-old woman with indigestion has been taking her friend's omeprazole for the...

    Correct

    • A 35-year-old woman with indigestion has been taking her friend's omeprazole for the past week, which has improved her symptoms. You want to check for the presence of Helicobacter pylori by using a stool antigen test (SAT) or a carbon-13-labelled urea breath test (UBT). What is the recommended waiting period after stopping a proton pump inhibitor (PPI) before conducting these tests?

      Your Answer: 2-week washout period for either UBT or SAT

      Explanation:

      H. pylori Testing and Treatment Guidelines

      To ensure accurate diagnosis and appropriate treatment for H. pylori infection, it is recommended that adults with dyspepsia or reflux symptoms undergo a 2-week washout period before testing for H. pylori if they are receiving PPI therapy. This applies to both the carbon-13-labelled urea breath test (UBT) and stool antigen test (SAT). Testing should not be performed within two weeks of PPI use, as this can lead to false negatives.

      Patients with dyspepsia should be offered H. pylori ‘test and treat’ using a UBT, SAT, or laboratory-based serology. Office-based serological tests should not be used due to their inadequate performance. Retesting for eradication should be performed using a UBT, as there is insufficient evidence to recommend the SAT for this purpose.

      First-line treatment for H. pylori eradication involves a 7-day, twice-daily course of a PPI, amoxicillin, and either clarithromycin or metronidazole. Multiple regimens are available, and local protocols should be consulted.

      Guidelines for Accurate H. pylori Testing and Treatment

    • This question is part of the following fields:

      • Gastroenterology/Nutrition
      143.3
      Seconds
  • Question 3 - A 72-year-old man is brought in by ambulance after being found on the...

    Correct

    • A 72-year-old man is brought in by ambulance after being found on the floor early in the morning. He states that he tripped and fell in the evening and could not get up or get help. The following U&Es were taken:

      Na+ 135 mmol/l
      K+ 5.7 mmol/l
      Creatinine 347 mmol/l
      Urea 9.8 mmol/l
      Creatine kinase 14,550 I/U

      What could be the possible reason for this clinical presentation?

      Your Answer: Rhabdomyolysis

      Explanation:

      If someone is stuck on the ground for an extended period after falling, they may develop rhabdomyolysis. This condition occurs when myoglobin, a toxic substance released from muscle tissue, damages the kidneys and causes acute kidney injury. Elevated levels of creatinine kinase and potassium are common indicators of rhabdomyolysis.

      Rhabdomyolysis is a condition that may be presented in an exam scenario where a patient has experienced a fall or prolonged epileptic seizure and is discovered to have an acute kidney injury upon admission. The condition is characterized by a disproportionately elevated creatinine level, elevated creatine kinase (CK), myoglobinuria, hypocalcaemia (as myoglobin binds calcium), elevated phosphate (released from myocytes), hyperkalaemia (which may develop before renal failure), and metabolic acidosis. The causes of rhabdomyolysis include seizure, collapse or coma (such as an elderly patient collapsing at home and being found eight hours later), ecstasy use, crush injury, McArdle’s syndrome, and certain drugs, such as statins (especially if co-prescribed with clarithromycin).

      The management of rhabdomyolysis involves administering intravenous fluids to maintain good urine output, and urinary alkalinization may be used in some cases. It is important to recognize the signs and symptoms of rhabdomyolysis early on to prevent further complications and ensure prompt treatment.

    • This question is part of the following fields:

      • Renal Medicine/Urology
      51.9
      Seconds
  • Question 4 - A 55-year-old man presents to the Emergency Department with a 2-day history of...

    Correct

    • A 55-year-old man presents to the Emergency Department with a 2-day history of malaise, fever and night sweats. He also complains that he has recently developed increased sensitivity in his fingertips and states that every time he touches something his fingers hurt.
      His past medical history includes diabetes and end-stage chronic kidney disease, for which he receives regular haemodialysis. His parameters include a blood pressure of 130/95 mmHg, oxygen saturation of 98%, heart rate 120 bpm and a temperature of 38.2°C.
      Which of the following investigations would be needed to make a diagnosis?
      Select the SINGLE best investigation from the list below.
      Select ONE option only.

      Your Answer: Echocardiogram

      Explanation:

      Diagnostic Tests for a Patient with Suspected Infective Endocarditis

      Suspected infective endocarditis (IE) requires a thorough diagnostic workup to confirm the diagnosis and rule out other potential conditions. One of the major symptoms of IE is the development of Osler nodes, which are tender lumps found on the fingers and toes. Here are some diagnostic tests that may be used to evaluate a patient with suspected IE:

      Echocardiogram

      An echocardiogram is a crucial diagnostic test for IE. It is used to detect any abnormalities in the heart valves or chambers that may indicate the presence of IE. The modified Duke’s criteria, which are used to diagnose IE, include echocardiography as one of the major criteria.

      Nerve Conduction Studies

      Nerve conduction studies are used to detect any damage to the peripheral nerves. While this test may be used to evaluate conditions such as carpal tunnel syndrome or sciatica, it is not typically used to diagnose IE. In this case, the painful sensation in the fingertips is more likely due to Osler nodes than an underlying neurological disorder.

      Chest X-ray

      A chest X-ray is not typically indicated in a patient with suspected IE. While pneumonia may present with symptoms similar to those of IE, such as fever and malaise, other symptoms such as coughing and sputum production are more indicative of pneumonia.

      Mantoux Test

      The Mantoux test is used to detect latent tuberculosis (TB). While TB may present with symptoms similar to those of IE, such as night sweats and fever, a Mantoux test is not typically used to diagnose IE. In this case, the lack of risk factors for TB and the presence of Osler nodes suggest a diagnosis of IE.

      Sputum Culture

      A sputum culture may be used to diagnose respiratory conditions such as pneumonia. However, in a patient without a cough, a sputum culture is less likely to confirm a diagnosis. Other symptoms such as coughing and sputum production are more indicative of pneumonia.

    • This question is part of the following fields:

      • Cardiovascular
      16
      Seconds
  • Question 5 - A 42-year-old patient with ankylosing spondylitis complains of sudden pain in the right...

    Correct

    • A 42-year-old patient with ankylosing spondylitis complains of sudden pain in the right eye and blurry vision. During examination, you observe redness around the cornea and a constricted pupil. Ophthalmoscopy reveals difficulty in visualizing the retina due to the patient's intolerance to bright light, but you do notice a fluid level at the front of the eye. What is the probable diagnosis?

      Your Answer: Anterior uveitis

      Explanation:

      Anterior uveitis, also known as iritis, is a type of inflammation that affects the iris and ciliary body in the front part of the uvea. It is a common cause of red eye and is associated with HLA-B27, which may also be linked to other conditions. Symptoms of anterior uveitis include sudden onset of eye discomfort and pain, small or irregular pupils, intense sensitivity to light, blurred vision, redness, tearing, and the presence of pus and inflammatory cells in the front part of the eye. This condition may be associated with ankylosing spondylitis, reactive arthritis, ulcerative colitis, Crohn’s disease, Behcet’s disease, and sarcoidosis. Urgent review by an ophthalmologist is necessary, and treatment may involve the use of cycloplegics and steroid eye drops.

    • This question is part of the following fields:

      • Ophthalmology
      16.7
      Seconds
  • Question 6 - You are a foundation year 2 doctor on your GP placement. You see...

    Correct

    • You are a foundation year 2 doctor on your GP placement. You see 8-year-old Lily whose mother has brought her to see you as she feels Lily is snoring very loudly and wonders whether this is affecting her quality of sleep. Lily is overweight and has a background of childhood asthma.
      What is a frequent cause of snoring in childhood?

      Your Answer: Obesity

      Explanation:

      Snoring in Children: Possible Causes

      Snoring in children can be caused by various factors. One of the common causes is obesity, which can lead to the narrowing of the airways and difficulty in breathing during sleep. Another possible cause is nasal problems such as polyps, deviated septum, and hypertrophic nasal turbinates, which can also obstruct the airways and cause snoring. Recurrent tonsillitis can also contribute to snoring, as the inflamed tonsils can block the air passages.

      In some cases, snoring in children may be associated with certain medical conditions such as Down’s syndrome and hypothyroidism. These conditions can affect the structure and function of the respiratory system, leading to snoring and other breathing difficulties.

      It is important to identify the underlying cause of snoring in children and seek appropriate treatment to prevent potential health complications. Parents should consult a healthcare professional if their child snores regularly or experiences other symptoms such as daytime sleepiness, difficulty concentrating, or behavioral problems.

    • This question is part of the following fields:

      • Paediatrics
      74.3
      Seconds
  • Question 7 - A 35-year-old woman presents for review at her local general practice surgery. She...

    Correct

    • A 35-year-old woman presents for review at her local general practice surgery. She has noticed a number of patches of pale skin on her hands over the past few weeks. The patient has tried using emollients and topical clotrimazole with no result.
      On examination, a number of depigmented patches on the dorsum of both hands are noted. Her past medical history includes thyrotoxicosis for which she takes carbimazole and thyroxine.
      Given the likely diagnosis, which of the following is most appropriate before starting treatment?
      Select the SINGLE best option from the list below.
      Select ONE option only.

      Your Answer: No further testing required

      Explanation:

      Understanding Vitiligo: Diagnosis and Testing

      Vitiligo is an autoimmune condition that causes depigmentation of the skin due to the loss of melanocytes. It is usually diagnosed based on clinical features, such as well-demarcated patches of depigmented skin. While there are no specific diagnostic tests for vitiligo, a punch biopsy may be used to obtain a skin sample for histological analysis in cases of suspected skin cancer or inflammatory skin disease. However, skin patch testing and skin prick testing are not useful in diagnosing vitiligo.

      It is important to note that vitiligo is commonly associated with other autoimmune conditions, such as type I diabetes mellitus, Addison’s disease, thyroid disorders, pernicious anemia, and alopecia areata. While it can affect individuals of any age, it often arises before the age of 20 years and is equally prevalent in men and women. Itching and other symptoms are rare, and the changes may be more noticeable in individuals with light skin during the summer months.

      In contrast, a radioallergosorbent test (RAST) is unsuitable for diagnosing vitiligo as it is used to determine the amount of immunoglobulin E (IgE) that reacts with suspected or known allergens. RAST is useful for diagnosing food allergies, inhaled allergens, and venom allergies. Blood tests may be used when skin prick tests are not suitable, such as when the patient is taking antihistamines or has extensive eczema.

      In summary, vitiligo is a clinical diagnosis that does not require further testing. While a punch biopsy may be used in certain cases, skin patch testing and skin prick testing are not useful in diagnosing vitiligo. It is important to be aware of the potential association with other autoimmune conditions and to monitor for any changes in skin pigmentation.

    • This question is part of the following fields:

      • Dermatology
      135.5
      Seconds
  • Question 8 - A 35-year-old woman has recently undergone blood monitoring for hypothyroidism. She is currently...

    Correct

    • A 35-year-old woman has recently undergone blood monitoring for hypothyroidism. She is currently on a 100 micrograms dose of levothyroxine and her last blood tests showed normal levels of thyroid-stimulating hormone (TSH) and free thyroxine (ft4). However, her TSH has now risen to 8mU/L with ft4 slightly below the reference range. The patient confirms that she has been taking her levothyroxine as prescribed. You decide to review her recent medications to identify any potential causes for the suboptimal hypothyroidism treatment. What new medication could be responsible for this?

      Your Answer: Ferrous sulphate

      Explanation:

      To avoid reducing the absorption of levothyroxine, it is important to give iron/calcium carbonate tablets at least four hours apart from the medication. Ferrous sulphate is the medication that can affect the absorption of levothyroxine and should also be given four hours apart. Patients should be advised to separate doses of calcium carbonate or antacids containing aluminium and magnesium from levothyroxine by at least four hours. It is recommended to review potential drug interactions before increasing treatment doses and refer to The National Institute for Health and Care Excellence (NICE) clinical knowledge summaries for a detailed list of potential drug interactions. The other medications listed do not have a known effect on the absorption of levothyroxine.

      Managing Hypothyroidism: Dosage, Monitoring, and Side-Effects

      Hypothyroidism is a condition where the thyroid gland does not produce enough thyroid hormone. The main treatment for hypothyroidism is levothyroxine, a synthetic form of thyroid hormone. When managing hypothyroidism, it is important to consider the patient’s age, cardiac history, and initial starting dose. Elderly patients and those with ischaemic heart disease should start with a lower dose of 25mcg od, while other patients can start with 50-100mcg od. After a change in dosage, thyroid function tests should be checked after 8-12 weeks to ensure the therapeutic goal of normalising the thyroid stimulating hormone (TSH) level is achieved. The target TSH range is 0.5-2.5 mU/l.

      Women with hypothyroidism who become pregnant should have their dose increased by at least 25-50 micrograms levothyroxine due to the increased demands of pregnancy. The TSH should be monitored carefully, aiming for a low-normal value. It is important to note that there is no evidence to support combination therapy with levothyroxine and liothyronine.

      While levothyroxine is generally well-tolerated, there are some potential side-effects to be aware of. Over-treatment can lead to hyperthyroidism, while long-term use can reduce bone mineral density. In patients with cardiac disease, levothyroxine can worsen angina and lead to atrial fibrillation. It is also important to be aware of drug interactions, particularly with iron and calcium carbonate, which can reduce the absorption of levothyroxine. These medications should be given at least 4 hours apart.

      In summary, managing hypothyroidism involves careful consideration of dosage, monitoring of TSH levels, and awareness of potential side-effects and drug interactions. With appropriate management, patients with hypothyroidism can achieve normal thyroid function and improve their overall health.

    • This question is part of the following fields:

      • Endocrinology/Metabolic Disease
      358.1
      Seconds
  • Question 9 - Which one of the following regarding the FAST questionnaire for alcohol misuse is...

    Incorrect

    • Which one of the following regarding the FAST questionnaire for alcohol misuse is correct?

      Your Answer: The minimum score is 4

      Correct Answer: May be stopped after first question depending on the answer

      Explanation:

      Alcohol Problem Drinking: Detection and Assessment

      Alcohol problem drinking can have serious consequences on an individual’s health and well-being. Therefore, it is important to detect and assess problem drinking early on. Screening tools such as AUDIT, FAST, and CAGE can be used to identify individuals who may have hazardous or harmful alcohol consumption or alcohol dependence.

      AUDIT is a 10-item questionnaire that takes about 2-3 minutes to complete. It has been shown to be superior to CAGE and biochemical markers for predicting alcohol problems. A score of 8 or more in men, and 7 or more in women, indicates a strong likelihood of hazardous or harmful alcohol consumption. A score of 15 or more in men, and 13 or more in women, is likely to indicate alcohol dependence. AUDIT-C is an abbreviated form consisting of 3 questions.

      FAST is a 4-item questionnaire with a minimum score of 0 and a maximum score of 16. The score for hazardous drinking is 3 or more. Over 50% of people will be classified using just the first question, which asks how often the individual has had eight or more drinks on one occasion (or six or more drinks for women).

      CAGE is a well-known screening test, but recent research has questioned its value. Two or more positive answers are generally considered a ‘positive’ result. The questions ask if the individual has ever felt the need to cut down on their drinking, if people have annoyed them by criticizing their drinking, if they have ever felt guilty about their drinking, and if they have ever had a drink in the morning to get rid of a hangover.

      To diagnose alcohol dependence, the ICD-10 definition requires three or more of the following: compulsion to drink, difficulties controlling alcohol consumption, physiological withdrawal, tolerance to alcohol, neglect of alternative activities to drinking, and persistent use of alcohol despite evidence of harm.

      Overall, using screening tools and diagnostic criteria can help healthcare professionals identify individuals with alcohol problem drinking and provide appropriate interventions and support.

    • This question is part of the following fields:

      • Psychiatry
      59
      Seconds
  • Question 10 - A 32-year-old woman has come in for her 6-week baby check with no...

    Correct

    • A 32-year-old woman has come in for her 6-week baby check with no postnatal issues. She is currently breastfeeding and has a history of frequent migraines. She is seeking treatment for a migraine today. Which of the following medications should be avoided?

      Your Answer: Aspirin

      Explanation:

      Breastfeeding mothers should avoid taking aspirin as it may increase the risk of Reye’s syndrome. High doses of aspirin can also affect platelet function and cause hypoprothrombinaemia in infants with low vitamin K stores. However, paracetamol is safe to use for pain relief during breastfeeding. Anti-emetics such as cyclizine and prochlorperazine are also safe to use while breastfeeding and are unlikely to cause any harm.

      Breastfeeding has some contraindications that are important to know, especially when it comes to drugs. Antibiotics like penicillins, cephalosporins, and trimethoprim are safe for breastfeeding mothers, as are endocrine drugs like glucocorticoids (in low doses) and levothyroxine. Epilepsy drugs like sodium valproate and carbamazepine, asthma drugs like salbutamol and theophyllines, and hypertension drugs like beta-blockers and hydralazine are also safe. Anticoagulants like warfarin and heparin, as well as digoxin, are also safe. However, some drugs should be avoided, such as antibiotics like ciprofloxacin, tetracycline, chloramphenicol, and sulphonamides, psychiatric drugs like lithium and benzodiazepines, aspirin, carbimazole, methotrexate, sulfonylureas, cytotoxic drugs, and amiodarone. Other contraindications include galactosaemia and viral infections, although the latter is controversial in the developing world due to the increased risk of infant mortality and morbidity associated with bottle feeding.

    • This question is part of the following fields:

      • Neurology
      125.3
      Seconds
  • Question 11 - A 50-year-old woman presents to the ear, nose and throat clinic with a...

    Correct

    • A 50-year-old woman presents to the ear, nose and throat clinic with a 4-month history of left-sided hearing loss. She reports occasional ringing in her left ear and feeling unsteady. She has a medical history of well-controlled type 1 diabetes and denies any recent infections.

      During the examination, Rinne's test is positive in both ears, and Weber's test lateralizes to her right ear. There is no evidence of nystagmus, and her coordination is normal. Other than an absent left-sided corneal reflex, her cranial nerve examination is unremarkable.

      What is the most likely diagnosis?

      Your Answer: Acoustic neuroma

      Explanation:

      If a patient presents with a loss of corneal reflex, an acoustic neuroma should be considered as a possible cause. This is a benign tumor that affects the vestibulocochlear nerve and can lead to symptoms such as vertigo, tinnitus, and unilateral sensorineural hearing loss. In some cases, the tumor can also invade the trigeminal nerve, resulting in an absent corneal reflex.

      Other conditions that may cause hearing loss and vertigo include cholesteatoma, labyrinthitis, and Meniere’s disease. However, in this case, the patient’s hearing tests indicate a sensorineural hearing loss, which makes cholesteatoma less likely. Labyrinthitis typically causes acute vertigo that can persist for several days, but it would not be the cause of the loss of the corneal reflex. Meniere’s disease is characterized by a triad of symptoms, including tinnitus, vertigo, and sensorineural hearing loss, but the vertigo tends to be shorter in duration and follow a relapsing and remitting course.

      Understanding Vestibular Schwannoma (Acoustic Neuroma)

      Vestibular schwannoma, also known as acoustic neuroma, is a type of brain tumor that accounts for 5% of intracranial tumors and 90% of cerebellopontine angle tumors. The condition is characterized by a combination of symptoms such as vertigo, hearing loss, tinnitus, and an absent corneal reflex. The affected cranial nerves can predict the features of the condition. For instance, cranial nerve VIII can cause vertigo, unilateral sensorineural hearing loss, and unilateral tinnitus. On the other hand, cranial nerve V can lead to an absent corneal reflex, while cranial nerve VII can cause facial palsy.

      Bilateral vestibular schwannomas are often seen in neurofibromatosis type 2. The diagnosis of vestibular schwannoma is made through an MRI of the cerebellopontine angle, and audiometry is also important since only 5% of patients have a normal audiogram.

      The management of vestibular schwannoma involves surgery, radiotherapy, or observation. The choice of treatment depends on the size and location of the tumor, the patient’s age and overall health, and the severity of symptoms. In conclusion, understanding vestibular schwannoma is crucial in managing the condition effectively.

    • This question is part of the following fields:

      • ENT
      117.4
      Seconds
  • Question 12 - A 27-year-old man visits his GP and insists on getting a CT scan...

    Correct

    • A 27-year-old man visits his GP and insists on getting a CT scan of his abdomen, claiming that he is certain he has cancer despite previous negative test results. What type of disorder does this behavior exemplify?

      Your Answer: Hypochondrial disorder

      Explanation:

      Somatisation refers to the manifestation of physical symptoms that cannot be explained by any underlying medical condition. On the other hand, hypochondria is a condition where a person constantly worries about having a serious illness, often believing that minor symptoms are signs of a life-threatening disease such as cancer.

      Psychiatric Terms for Unexplained Symptoms

      There are various psychiatric terms used to describe patients who exhibit symptoms for which no organic cause can be found. One such disorder is somatisation disorder, which involves the presence of multiple physical symptoms for at least two years, and the patient’s refusal to accept reassurance or negative test results. Another disorder is illness anxiety disorder, which is characterized by a persistent belief in the presence of an underlying serious disease, such as cancer, despite negative test results.

      Conversion disorder is another condition that involves the loss of motor or sensory function, and the patient does not consciously feign the symptoms or seek material gain. Patients with this disorder may be indifferent to their apparent disorder, a phenomenon known as la belle indifference. Dissociative disorder, on the other hand, involves the process of ‘separating off’ certain memories from normal consciousness, and may manifest as amnesia, fugue, or stupor. Dissociative identity disorder (DID) is the most severe form of dissociative disorder and was previously known as multiple personality disorder.

      Factitious disorder, also known as Munchausen’s syndrome, involves the intentional production of physical or psychological symptoms. Finally, malingering is the fraudulent simulation or exaggeration of symptoms with the intention of financial or other gain. Understanding these psychiatric terms can help healthcare professionals better diagnose and treat patients with unexplained symptoms.

    • This question is part of the following fields:

      • Psychiatry
      102.4
      Seconds
  • Question 13 - A 35-year-old woman presents with lethargy, arthralgia and a facial rash and is...

    Correct

    • A 35-year-old woman presents with lethargy, arthralgia and a facial rash and is diagnosed with systemic lupus erythematosus. Her rheumatologist initiates treatment with hydroxychloroquine. What is the most crucial parameter to monitor during her treatment?

      Your Answer: Visual acuity

      Explanation:

      The use of hydroxychloroquine can lead to a serious and irreversible retinopathy.

      Hydroxychloroquine: Uses and Adverse Effects

      Hydroxychloroquine is a medication commonly used in the treatment of rheumatoid arthritis and systemic/discoid lupus erythematosus. It is similar to chloroquine, which is used to treat certain types of malaria. However, hydroxychloroquine has been found to cause bull’s eye retinopathy, which can result in severe and permanent visual loss. Recent data suggests that this adverse effect is more common than previously thought, and the most recent guidelines recommend baseline ophthalmological examination and annual screening, including colour retinal photography and spectral domain optical coherence tomography scanning of the macula. Despite this risk, hydroxychloroquine may still be used in pregnant women if needed. Patients taking this medication should be asked about visual symptoms and have their visual acuity monitored annually using a standard reading chart.

    • This question is part of the following fields:

      • Musculoskeletal
      49.4
      Seconds
  • Question 14 - A 15-year-old boy presents to his General Practitioner as he has been suffering...

    Correct

    • A 15-year-old boy presents to his General Practitioner as he has been suffering from recurrent infections for the last few months. He has also been losing weight. He has taken four courses of antibiotics in the last six months for various respiratory tract infections. He also experienced an episode of shingles that took a few years to clear after becoming secondarily infected.
      On examination, he is pale and underweight, with a body mass index (BMI) of 17.5 kg/m2. He has fine, downy hair on his back, abdomen and forearms. His temperature is 35.9 °C. His blood pressure is 90/45 mmHg while his pulse is 52 bpm.
      What is the most likely cause of this patient’s immunodeficiency?

      Your Answer: Malnutrition

      Explanation:

      Differential diagnosis of immunodeficiency in an adolescent with weight loss and recurrent infection

      Malnutrition, primary immunodeficiency, cytomegalovirus (CMV) infection, human immunodeficiency virus (HIV) infection, and diabetes mellitus are among the possible causes of immunodeficiency in an adolescent with weight loss and recurrent infection. Malnutrition can suppress the immune system and is often associated with anorexia nervosa, which can be characterized by a very low body mass index (BMI), lanugo hair growth, hypothermia, bradycardia, and hypotension. Primary immunodeficiency syndromes, which are usually inherited as single-gene disorders, tend to present in infancy or early childhood with poor growth and weight gain and recurrent, prolonged, severe, or atypical infections. Cytomegalovirus (CMV) is a herpes virus that can cause serious complications in immunocompromised individuals or congenital cases, but is usually asymptomatic in immunocompetent individuals. Human immunodeficiency virus (HIV) infection can result in immunodeficiency by infecting and destroying CD4 cells, and should be suspected in individuals with prolonged, severe, or recurrent infections, particularly if they are a member of a high-risk group. Diabetes mellitus, especially type I, can also cause dysfunction of the immune system and increase the risk of infection. However, in an adolescent with a low BMI, type II diabetes would be very unlikely.

    • This question is part of the following fields:

      • Immunology/Allergy
      48.7
      Seconds
  • Question 15 - A 35-year-old woman experiences hypertension during the third trimester of her initial pregnancy....

    Correct

    • A 35-year-old woman experiences hypertension during the third trimester of her initial pregnancy. Upon conducting a 24-hour urine collection, it is revealed that she has 0.5g protein. Which of the following complications is the least commonly associated with this condition?

      Your Answer: Transverse myelitis

      Explanation:

      Transverse myelitis is not linked to pre-eclampsia.

      Pre-eclampsia is a condition that occurs during pregnancy and is characterized by high blood pressure, proteinuria, and edema. It can lead to complications such as eclampsia, neurological issues, fetal growth problems, liver involvement, and cardiac failure. Severe pre-eclampsia is marked by hypertension, proteinuria, headache, visual disturbances, and other symptoms. Risk factors for pre-eclampsia include hypertension in a previous pregnancy, chronic kidney disease, autoimmune disease, diabetes, chronic hypertension, first pregnancy, and age over 40. Aspirin may be recommended for women with high or moderate risk factors. Treatment involves emergency assessment, admission for observation, and medication such as labetalol, nifedipine, or hydralazine. Delivery of the baby is the most important step in management, with timing depending on the individual case.

    • This question is part of the following fields:

      • Reproductive Medicine
      32.1
      Seconds
  • Question 16 - An 80-year-old man is brought to the emergency department by ambulance after being...

    Correct

    • An 80-year-old man is brought to the emergency department by ambulance after being found on the floor at home. He is disoriented and unable to provide a clear history. His relatives are yet to arrive. He has a GCS of 12. On examination you note crackles at the left base on auscultation, an ejection systolic murmur over the left sternal edge, and a soft, nontender abdomen. His right pupil is slightly dilated compared to the left and is sluggish to react to light. He has no obvious injuries.
      What is the most appropriate, immediate source of action to aid in diagnosis?

      Your Answer: CT brain

      Explanation:

      Immediate CT scan is necessary to evaluate for raised intracranial pressure and tentorial herniation in a patient with a sluggishly responsive unilaterally dilated pupil. This is the most pressing concern, given the patient’s reduced GCS. Although other investigations will be necessary, the CT brain is the most critical test, as the patient may require urgent neurosurgical intervention to save their life.

      Patients with head injuries should be managed according to ATLS principles and extracranial injuries should be managed alongside cranial trauma. There are different types of traumatic brain injuries, including extradural hematoma, subdural hematoma, and subarachnoid hemorrhage. Primary brain injury may be focal or diffuse, and secondary brain injury can occur due to cerebral edema, ischemia, infection, or herniation. Management may include IV mannitol/frusemide, decompressive craniotomy, and ICP monitoring. Pupillary findings can provide information on the location and severity of the injury.

    • This question is part of the following fields:

      • Neurology
      223.6
      Seconds
  • Question 17 - A 55-year-old man presents to his General Practitioner after experiencing buzzing sounds in...

    Correct

    • A 55-year-old man presents to his General Practitioner after experiencing buzzing sounds in both ears intermittently over the past two weeks. He claims that this occurs suddenly, lasts for a few seconds and is not associated with his pulse. He reports no change in his hearing or other symptoms. Ear and cranial nerve examinations are unremarkable.
      Which of the following investigations are necessary?

      Your Answer: Audiogram

      Explanation:

      Investigating Tinnitus: Guidelines and Recommendations

      Tinnitus, the perception of sounds in the ears or head that do not come from an outside source, affects around 1 in 10 people at some point in their life. While it is sometimes considered a minor symptom of ringing in the ears, it can be distressing and may indicate a serious underlying condition. Here are some guidelines and recommendations for investigating tinnitus:

      Audiological Assessment: The National Institute for Health and Care Excellence (NICE) recommends that all patients with tinnitus should be offered an audiological assessment.

      Psychoacoustic Testing: Acoustic reflex testing and psychoacoustic testing are not recommended as part of the investigation of tinnitus.

      Imaging: Imaging should not be offered to people with symmetrical non-pulsatile tinnitus with no associated neurological, audiological, otological or head-and-neck signs and symptoms. If they are unable to have this, a contrast-enhanced CT scan of the internal auditory meatus should be offered. An MR scan of the internal auditory meatus should only be offered to people with unilateral or asymmetrical non-pulsatile tinnitus, or non-pulsatile tinnitus with associated neurological, otological or head-and-neck signs and symptoms.

      Otoacoustic Emissions: Otoacoustic emission testing should only be considered if there are other indicative symptoms and signs. All patients with tinnitus should be offered an audiological assessment.

    • This question is part of the following fields:

      • ENT
      96.3
      Seconds
  • Question 18 - A 28-year-old pregnant woman goes to her first prenatal appointment and is found...

    Correct

    • A 28-year-old pregnant woman goes to her first prenatal appointment and is found to have a urinary tract infection based on a urine dipstick test. Despite being asymptomatic, which antibiotic should she steer clear of during the first trimester of pregnancy?

      Your Answer: Trimethoprim

      Explanation:

      Urinary tract infections in pregnancy should be treated to prevent pyelonephritis. Trimethoprim should be avoided in the first trimester due to teratogenicity risk. Erythromycin is not typically used for UTIs and nitrofurantoin should be avoided close to full term. Sulfonamides and quinolones should also be avoided in pregnancy.

      Urinary tract infections (UTIs) are common in adults and can affect different parts of the urinary tract. The management of UTIs depends on various factors such as the patient’s age, gender, and pregnancy status. For non-pregnant women, local antibiotic guidelines should be followed if available. Trimethoprim or nitrofurantoin for three days are recommended by NICE Clinical Knowledge Summaries. However, if the patient is aged over 65 years or has visible or non-visible haematuria, a urine culture should be sent. Pregnant women with UTIs should be treated with nitrofurantoin, amoxicillin, or cefalexin for seven days. Trimethoprim should be avoided during pregnancy as it is teratogenic in the first trimester. Asymptomatic bacteriuria in pregnant women should also be treated to prevent progression to acute pyelonephritis. Men with UTIs should be offered a seven-day course of trimethoprim or nitrofurantoin unless prostatitis is suspected. A urine culture should be sent before antibiotics are started. Catheterised patients should not be treated for asymptomatic bacteria, but if symptomatic, a seven-day course of antibiotics should be given. Acute pyelonephritis requires hospital admission and treatment with a broad-spectrum cephalosporin or quinolone for 10-14 days. Referral to urology is not routinely required for men who have had one uncomplicated lower UTI.

    • This question is part of the following fields:

      • Reproductive Medicine
      14.6
      Seconds
  • Question 19 - An older patient with Bell's palsy presented to the emergency department with complaints...

    Correct

    • An older patient with Bell's palsy presented to the emergency department with complaints of a sore and gritty right eye. Despite occasional blurring of vision, the patient's visual acuity remained unaffected. The patient was unable to close their right eye and had not been compliant with taping the eyelid at night or using the lubricating ointment provided by their GP a week prior. An ophthalmologist performed a slit lamp examination, which revealed a normal-appearing cornea and anterior chamber. The examination was then continued with the addition of fluorescein dye on the eye. What findings would the doctor anticipate during this examination?

      Your Answer: Punctate fluorescein staining of cornea

      Explanation:

      Patients with dry eyes often exhibit punctate fluorescein staining of the cornea, which is a common occurrence in those with Bell’s palsy. This condition impairs the ability to blink or close the eye, leading to a lack of moisture on the cornea and subsequent dryness. It is important to note that keratic precipitates and foreign bodies can be observed without the use of fluorescein dye, and keratic precipitates are typically associated with anterior uveitis rather than the dry eye syndrome seen in Bell’s palsy. Additionally, corneal abrasions typically result in decreased visual acuity, which is not a symptom of dry eyes in this context.

      Understanding Dry Eye Syndrome

      Dry eye syndrome is a condition that causes discomfort in both eyes, with symptoms such as dryness, grittiness, and soreness that worsen throughout the day. Exposure to wind can also cause watering of the eyes. People with Meibomian gland dysfunction may experience symptoms that are worse upon waking, with eyelids sticking together and redness of the eyelids. In some cases, dry eye syndrome can lead to complications such as conjunctivitis or corneal ulceration, which can cause severe pain, photophobia, redness, and loss of visual acuity.

      Although there may be no abnormalities on examination, eyelid hygiene is the most appropriate management step for dry eye syndrome. This can help control blepharitis, which is a common condition associated with dry eye syndrome. By understanding the symptoms and appropriate management steps, individuals with dry eye syndrome can find relief and improve their overall eye health.

    • This question is part of the following fields:

      • Ophthalmology
      45.4
      Seconds
  • Question 20 - A woman in her early stages of pregnancy seeks guidance on whether it...

    Correct

    • A woman in her early stages of pregnancy seeks guidance on whether it is safe to consume alcohol. What advice aligns with the current NICE guidelines?

      Your Answer: Avoid alcohol throughout pregnancy

      Explanation:

      Antenatal care guidelines were issued by NICE in March 2008, which included specific points for the care of healthy pregnant women. Nausea and vomiting can be treated with natural remedies such as ginger and acupuncture on the ‘p6’ point, as recommended by NICE. Antihistamines, with promethazine as the first-line option according to the BNF, can also be used. Adequate vitamin D intake is crucial for the health of both the mother and baby, and women should be informed about this at their booking appointment. The Chief Medical Officer advises all pregnant and breastfeeding women to take a daily supplement containing 10 micrograms of vitamin D, with particular care taken for those at risk. In 2016, new guidelines were proposed by the Chief Medical Officer regarding alcohol consumption during pregnancy. The government now advises pregnant women not to drink any alcohol to minimize the risk of harm to the baby.

    • This question is part of the following fields:

      • Reproductive Medicine
      22
      Seconds
  • Question 21 - A 58-year-old man contacts his General Practitioner to request a repeat prescription of...

    Correct

    • A 58-year-old man contacts his General Practitioner to request a repeat prescription of xylometazoline hydrochloride nasal spray. He has been using this for the past four weeks to 'clear up his sinuses.'
      What is the most likely side effect this patient will develop based on his current management?

      Your Answer: Rebound nasal congestion

      Explanation:

      Understanding the Side Effects of Long-Term Nasal Decongestant Use

      Nasal decongestants are a common treatment for nasal congestion, but long-term use can lead to adverse effects. One of the most significant risks is rebound nasal congestion, which can encourage further use and hypertrophy of the nasal mucosa. It is recommended to use nasal decongestants for a maximum of seven days to avoid this risk. Other adverse effects of long-term use include nasal burning, irritation, and dryness, but chronic rhinitis is not a recognized side effect. While cardiovascular effects like tachycardia and hypertension are possible, they are more common with oral decongestants. Septal perforation is a rare side effect of intranasal corticosteroids, not nasal decongestants. It is essential to understand the potential risks of long-term nasal decongestant use and to use them only as directed.

    • This question is part of the following fields:

      • ENT
      30.8
      Seconds
  • Question 22 - A 7-year-old girl is referred to the Paediatric Emergency Department by her General...

    Correct

    • A 7-year-old girl is referred to the Paediatric Emergency Department by her General Practitioner with a 4-day history of fever.
      On examination, the patient has bilateral conjunctival injection, a maculopapular rash across her trunk, and erythematous extremities. Her chest is clear and heart sounds are normal. The abdomen is soft and nontender. Her lips look cracked, and her tongue looks erythematous. She has no palpable lymphadenopathy.
      Which of the following blood test results would support the likely diagnosis for this patient?

      Your Answer: Thrombocytosis

      Explanation:

      Understanding Kawasaki Disease: Diagnosis and Blood Test Results

      Kawasaki disease is a clinical diagnosis that presents with a persistent fever and at least four of the following five criteria: bilateral conjunctival injection, polymorphous rash, oral changes, oedema and erythema in hands/feet, and cervical lymphadenopathy. Thrombocytosis is a common non-specific change seen in Kawasaki disease, and blood tests such as full blood count, urea and electrolytes, liver function, lipid profile, C-reactive protein (CRP), and erythrocyte sedimentation rate (ESR) can support the diagnosis, assess severity, and monitor disease and treatment. Neutropenia is not usually associated with Kawasaki disease, and a raised white cell count with a relative neutrophilia is commonly seen. An elevated CRP with a normal ESR or an elevated ESR with a normal CRP would not be expected in Kawasaki disease, as both markers reflect acute inflammation. Kawasaki disease is associated with normocytic anaemia, but not macrocytic anaemia. It is important to arrange an echocardiogram as soon as possible to look for any initial evidence of coronary artery aneurysm, a common complication of Kawasaki disease.

    • This question is part of the following fields:

      • Musculoskeletal
      114.8
      Seconds
  • Question 23 - A 42-year-old woman presents to the Emergency Department with retrosternal chest pain. She...

    Correct

    • A 42-year-old woman presents to the Emergency Department with retrosternal chest pain. She is admitted and all cardiac investigations are normal. She is diagnosed with gastro-oesophageal reflux disease.
      Which of the following symptoms would most commonly require an urgent inpatient upper gastrointestinal (GI) endoscopy before being discharged?

      Your Answer: Melaena

      Explanation:

      Melaena is a serious symptom of upper GI bleeding that requires emergency treatment. The patient must be stabilized and resuscitated before undergoing an upper GI endoscopy within 24 hours of admission. Dysphagia is a red-flag symptom that may indicate oesophageal or gastric cancer and requires urgent investigation with an upper GI endoscopy within two weeks. Epigastric pain without red-flag symptoms should be treated with PPIs for 4-8 weeks before any investigation is necessary. Vomiting with high platelet count, weight loss, reflux, dyspepsia, or upper-abdominal pain requires a non-urgent OGD. Weight loss in patients over 55 years with reflux symptoms requires a 2-week wait referral for suspected cancer, but not an urgent inpatient endoscopy.

    • This question is part of the following fields:

      • Gastroenterology/Nutrition
      13.7
      Seconds
  • Question 24 - As a physician on the night shift cardiac arrest team, you receive an...

    Correct

    • As a physician on the night shift cardiac arrest team, you receive an emergency page requesting immediate assistance on the geriatric ward. Upon arrival, you discover the nursing staff performing chest compressions on an unresponsive patient with no carotid pulse. You instruct them to continue compressions while you apply defibrillator pads to the patient's chest. After a brief pause in compressions, the defibrillator monitor displays a monomorphic, broad complex tachycardia. What is the next best course of action?

      Your Answer: Immediately give 1 defibrillator shock followed by CPR

      Explanation:

      When pulseless ventricular tachycardia (VT) is identified, the immediate and correct treatment is a single defibrillator shock followed by 2 minutes of CPR. This is in contrast to using intravenous adenosine or amiodarone, which are not appropriate in this scenario. The Resuscitation Council (UK) guidelines now recommend a single shock for ventricular fibrillation (VF) or pulseless VT. Administering 3 back-to-back shocks followed by 1 minute of CPR is part of the Advanced Life Support (ALS) algorithm, but it is not the most appropriate next step in management for a delayed recognition of rhythm like in the above case. In contrast, continued CPR with 30 chest compressions to 2 breaths is appropriate in a basic life support scenario where a defibrillator is not yet available.

      The 2015 Resus Council guidelines for adult advanced life support outline the steps to be taken when dealing with patients with shockable and non-shockable rhythms. For both types of patients, chest compressions are a crucial part of the process, with a ratio of 30 compressions to 2 ventilations. Defibrillation is recommended for shockable rhythms, with a single shock for VF/pulseless VT followed by 2 minutes of CPR. Adrenaline and amiodarone are the drugs of choice for non-shockable rhythms, with adrenaline given as soon as possible and amiodarone administered after 3 shocks for VF/pulseless VT. Thrombolytic drugs should be considered if a pulmonary embolus is suspected. Atropine is no longer recommended for routine use in asystole or PEA. Oxygen should be titrated to achieve saturations of 94-98% following successful resuscitation. The Hs and Ts should be considered as potential reversible causes of cardiac arrest.

    • This question is part of the following fields:

      • Cardiovascular
      281.9
      Seconds
  • Question 25 - The hand radiograph of a 43-year-old woman demonstrates periarticular osteoporosis, loss of joint...

    Correct

    • The hand radiograph of a 43-year-old woman demonstrates periarticular osteoporosis, loss of joint space and bone erosions.
      Which of the following is the most likely diagnosis?

      Your Answer: Rheumatoid arthritis (RA)

      Explanation:

      Radiographic Features of Common Rheumatologic Conditions

      Rheumatoid arthritis (RA) is characterized by periarticular osteoporosis, narrowing of joint space, juxta-articular bony erosions, subluxation, gross deformity, and periarticular soft tissue swelling. In the hands, swan neck deformity of fingers, ulnar deviation of the metacarpophalangeal (MCP) joints, boutonnière deformity of the thumb, and Bouchard’s nodes are common. However, the presence of Bouchard’s nodes without Heberden’s nodes is more indicative of RA than osteoarthritis.

      Gout may present with gouty tophi, which are soft tissue masses created by the deposition of urate crystals. Punched-out erosions caused by bone absorption may also be present. These changes tend to be sporadic and asymmetrical.

      Osteoarthritis is characterized by subchondral bone cysts, osteophytes, narrowing of joint space, and subchondral sclerosis. Clinically, both Heberden’s and Bouchard’s nodes may be present.

      Psoriatic arthritis most commonly affects the hands and feet. Radiographic features include erosions along the shaft of the phalanges, leading to ‘pencil-in-cup’ deformity and tufting of the bones. Unlike RA, osteoporosis is not a feature, and typically the more distal joints are affected.

      Hypercalcaemia does not have specific radiographic features. The changes seen would be those associated with the underlying cause of the hypercalcaemia, such as hyperparathyroidism or cancer.

    • This question is part of the following fields:

      • Musculoskeletal
      35.3
      Seconds
  • Question 26 - A 45-year-old non-smoker with hypertension and diabetes has been diagnosed with bilateral renal...

    Incorrect

    • A 45-year-old non-smoker with hypertension and diabetes has been diagnosed with bilateral renal artery stenosis. Blood tests reveal that he has normal renal function. He has undergone percutaneous angioplasty to both renal arteries, which was unsuccessful.
      Which medication should this patient be started on?

      Your Answer: Start spironolactone

      Correct Answer: Start angiotensin-converting enzyme (ACE) inhibitors

      Explanation:

      Medical Management of Renal Artery Stenosis

      Renal artery stenosis is a condition that requires medical management to control hypertension. Even if the arteries are treated successfully with angioplasty, antihypertensive therapy should be initiated. The ideal agent for this purpose is one that blocks the renin-angiotensin-aldosterone system, such as angiotensin-converting enzyme (ACE) inhibitors or angiotensin-receptor blockers (ARBs). Warfarin is not indicated in patients with renal artery stenosis, but may be used for prophylaxis of embolisation in other conditions. Clopidogrel is not indicated for hypertension management in renal artery stenosis. Statins may be used for primary prevention of cardiovascular disease if cholesterol levels are raised, but controlling blood pressure is the primary consideration in renal artery stenosis. Spironolactone should not be used in patients with renal compromise. Control of blood pressure should ideally be achieved using ACE inhibitors or ARBs.

    • This question is part of the following fields:

      • Renal Medicine/Urology
      36.9
      Seconds
  • Question 27 - Which of the following side-effects is more prevalent with atypical rather than conventional...

    Correct

    • Which of the following side-effects is more prevalent with atypical rather than conventional antipsychotics?

      Your Answer: Weight gain

      Explanation:

      Weight gain is a common side effect of atypical antipsychotics.

      Atypical antipsychotics are now recommended as the first-line treatment for patients with schizophrenia, as per the 2005 NICE guidelines. These medications have the advantage of significantly reducing extrapyramidal side-effects. However, they can also cause adverse effects such as weight gain, hyperprolactinaemia, and in the case of clozapine, agranulocytosis. The Medicines and Healthcare products Regulatory Agency has issued warnings about the increased risk of stroke and venous thromboembolism when antipsychotics are used in elderly patients. Examples of atypical antipsychotics include clozapine, olanzapine, risperidone, quetiapine, amisulpride, and aripiprazole.

      Clozapine, one of the first atypical antipsychotics, carries a significant risk of agranulocytosis and requires full blood count monitoring during treatment. Therefore, it should only be used in patients who are resistant to other antipsychotic medication. The BNF recommends introducing clozapine if schizophrenia is not controlled despite the sequential use of two or more antipsychotic drugs, one of which should be a second-generation antipsychotic drug, each for at least 6-8 weeks. Adverse effects of clozapine include agranulocytosis, neutropaenia, reduced seizure threshold, constipation, myocarditis, and hypersalivation. Dose adjustment of clozapine may be necessary if smoking is started or stopped during treatment.

    • This question is part of the following fields:

      • Psychiatry
      51.1
      Seconds
  • Question 28 - A 25-year-old man is brought to the Emergency Department by his friends. Around...

    Correct

    • A 25-year-old man is brought to the Emergency Department by his friends. Around 2 hours ago he was allegedly assaulted outside of a bar. He was repeatedly punched in the head and has sustained some bruising around his eyes. His friends report that he is 'concussed' and say that he is confused. On examination his GCS is 14 (M6 V4 E4) and he has trouble explaining where he is. There are no focal neurological features. There is no past medical history of note. Tonight he has drunk around four pints of lager. What is the most appropriate management with regards to a possible head injury?

      Your Answer: CT head scan within 1 hour

      Explanation:

      According to the latest NICE guidelines, a CT head scan is necessary for this patient as their GCS remains below 15 after 2 hours.

      NICE Guidelines for Investigating Head Injuries in Adults

      Head injuries can be serious and require prompt medical attention. The National Institute for Health and Care Excellence (NICE) has provided clear guidelines for healthcare professionals to determine which adult patients need further investigation with a CT head scan. Patients who require immediate CT head scans include those with a Glasgow Coma Scale (GCS) score of less than 13 on initial assessment, suspected open or depressed skull fractures, signs of basal skull fractures, post-traumatic seizures, focal neurological deficits, and more than one episode of vomiting.

      For patients with any loss of consciousness or amnesia since the injury, a CT head scan within 8 hours is recommended for those who are 65 years or older, have a history of bleeding or clotting disorders, experienced a dangerous mechanism of injury, or have more than 30 minutes of retrograde amnesia of events immediately before the head injury. Additionally, patients on warfarin who have sustained a head injury with no other indications for a CT head scan should also receive a scan within 8 hours of the injury.

      It is important for healthcare professionals to follow these guidelines to ensure that patients receive appropriate and timely care for their head injuries. By identifying those who require further investigation, healthcare professionals can provide the necessary treatment and support to prevent further complications and improve patient outcomes.

    • This question is part of the following fields:

      • Neurology
      64.7
      Seconds
  • Question 29 - A 25-year-old man visits his GP complaining of a rash that has spread...

    Correct

    • A 25-year-old man visits his GP complaining of a rash that has spread across his trunk over the last 4 days. He is worried about the appearance of the rash. The patient has no significant medical history except for completing a course of phenoxymethylpenicillin for tonsillitis last week and takes no other regular medications. Upon examination, the doctor observes multiple scaly papules on the patient's trunk and upper limbs. The lesions are small and have a teardrop shape. What is the most probable diagnosis?

      Your Answer: Guttate psoriasis

      Explanation:

      The tear-drop scaly papules that have suddenly appeared on the patient’s trunk and limbs suggest guttate psoriasis. This type of psoriasis is commonly seen in children and young adults who have recently had a Streptococcus infection, such as the tonsillitis infection that this patient had. The rash is characterized by multiple small scaly and red patches that have a teardrop shape.

      Disseminated varicella zoster, pityriasis rosea, and pityriasis versicolor are not likely diagnoses for this patient. Disseminated varicella zoster causes a different type of rash that includes macular, papular, and vesicular lesions that crust over time. Pityriasis rosea presents with a large round herald patch on the chest, abdomen, or back, and is thought to be triggered by viral or bacterial infections. Pityriasis versicolor is a fungal infection that causes patches that are paler than the surrounding skin, and is commonly found on the upper limbs and neck. However, exposure to heat and moisture can increase the risk of developing this rash.

      Guttate psoriasis is a type of psoriasis that is more commonly seen in children and adolescents. It is often triggered by a streptococcal infection that occurred 2-4 weeks prior to the appearance of the lesions. The name guttate comes from the Latin word for drop, as the lesions appear as small, tear-shaped papules on the trunk and limbs. These papules are pink and scaly, and the onset of the condition is usually acute, occurring over a few days.

      In most cases, guttate psoriasis will resolve on its own within 2-3 months. There is no clear evidence to support the use of antibiotics to treat the underlying streptococcal infection. Treatment options for guttate psoriasis include topical agents commonly used for psoriasis and UVB phototherapy. In cases where the condition recurs, a tonsillectomy may be necessary.

      It is important to differentiate guttate psoriasis from pityriasis rosea, another skin condition that can present with similar symptoms. Guttate psoriasis is often preceded by a streptococcal sore throat, while pityriasis rosea may be preceded by a respiratory tract infection. The appearance of guttate psoriasis is characterized by tear-shaped papules on the trunk and limbs, while pityriasis rosea presents with a herald patch followed by multiple oval lesions with a fine scale. While guttate psoriasis resolves within a few months, pityriasis rosea typically resolves after around 6 weeks.

    • This question is part of the following fields:

      • Dermatology
      71
      Seconds
  • Question 30 - A 23-year-old man is sent to your office for evaluation by his family....

    Incorrect

    • A 23-year-old man is sent to your office for evaluation by his family. The patient recently graduated from university and has had trouble adapting and fitting in. His parents note that he has always been a loner, preferring to stay in his room. They hoped graduation would bring him out of his shell. He has not made any new friends, but only his parents are bothered by this. Instead of socialising, he seems to have continued to stay alone in his room.
      On interview, he is withdrawn and quiet. His range of affect is restricted, and he displays no clear happiness or joy when discussing activities that he reports enjoying. He denies any auditory or visual hallucinations and has no suicidal or homicidal intent. He reports that he has no change in his sleep, appetite, energy or concentration.
      What is the most likely diagnosis in this patient?

      Your Answer: Avoidant personality disorder

      Correct Answer: Schizoid personality disorder

      Explanation:

      Understanding Schizoid Personality Disorder: Differentiating from Other Psychiatric Conditions

      Personality disorders are characterized by enduring patterns of perception, processing, and engagement that become ingrained, inflexible, and maladaptive. Schizoid personality disorder is a type of personality disorder that falls under the weird cluster of disorders. Patients with this disorder are withdrawn loners with flat affects, but they do not have weird/magical thinking (schizotypal) or psychotic symptoms (schizophrenia, schizoaffective disorder). They classically have a very flat affect and no interest in interpersonal relationships, preferring to work and play alone. It is important to differentiate schizoid personality disorder from other psychiatric conditions such as schizophrenia, avoidant personality disorder, schizoaffective disorder, and schizotypal personality disorder, as they have distinct features and treatment approaches.

    • This question is part of the following fields:

      • Psychiatry
      71.8
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SESSION STATS - PERFORMANCE PER SPECIALTY

Musculoskeletal (4/4) 100%
Gastroenterology/Nutrition (2/2) 100%
Renal Medicine/Urology (1/2) 50%
Cardiovascular (2/2) 100%
Ophthalmology (2/2) 100%
Paediatrics (1/1) 100%
Dermatology (2/2) 100%
Endocrinology/Metabolic Disease (1/1) 100%
Psychiatry (2/4) 50%
Neurology (3/3) 100%
ENT (3/3) 100%
Immunology/Allergy (1/1) 100%
Reproductive Medicine (3/3) 100%
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