random cases Flashcards

cases from everywhere! (not just MSK)

1
Q

A 20-year-old man presents to his primary care physician with low back pain and stiffness that has persisted for more than 3 months. There is no history of obvious injury but he is a very avid sportsman. His back symptoms are worse when he awakes in the morning, and the stiffness lasts more than 1 hour. His back symptoms improve with exercise. He has a desk job and finds that sitting for long periods of time exacerbates his symptoms. He has to get up regularly and move around. His back symptoms also wake him in the second half of the night, after which he can find it difficult to get comfortable. He normally takes an anti-inflammatory drug during the day, and finds his stiffness is worse when he misses a dose. He has had 2 bouts of iritis in the past.

A

ankylosing spondilitis

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2
Q

A 79-year-old man presents with dyspnoea on exertion for 1 year and lower extremity oedema. As part of a cardiac work-up, the echo shows concentric left ventricular hypertrophy. Cardiac catheterisation shows normal coronary arteries and he is referred for further evaluation of non-cardiac dyspnoea.

A

amyloidosis

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3
Q

A 62-year-old man is referred for management of atypical multiple myeloma. He has a mild anaemia of 120 g/L (12 g/dL), a urinary protein loss of 2.2 g/day with a urinary immunofixation showing free lambda light chains. However, the bone marrow shows only 5% plasma cells and does not fulfil criteria for multiple myeloma.

A

amyloidosis

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4
Q

A 54-year-old man complains of severe pain and swelling in his right first toe that developed overnight. He is limping because of the pain and states that this is the most severe pain he has ever had (‘even covering my foot with the bed sheet hurts’). He has had no previous episodes. His only medication is hydrochlorothiazide for hypertension. He drinks 2 to 3 beers a day. On examination, he is obese. There is swelling, erythema, warmth, and tenderness of the right first toe. There is also tenderness and warmth with mild swelling over the mid foot.

A

gout

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5
Q

An 85-year-old man presents with several days of swelling and severe pain in both hands limiting his ability to use his walking frame. He has a history of gout but has not experienced these symptoms before. On examination, he has a temperature of 37.8°C (100.1°F). There is diffuse warmth, mild erythema, and pitting oedema over the dorsum of both hands. There is tenderness and limited hand grip bilaterally. There are multiple nodules around several of the proximal interphalangeal and distal interphalangeal joints, and effusion and tenderness in his left olecranon bursa with palpable nodules.

A

gout -> acute bursitis

Gout may also present as acute bursitis, especially in the olecranon and prepatellar bursae. Chronic tophaceous gout may cause inflammatory destructive polyarthritis. This usually occurs in people with a long-standing history of attacks (mean 10 years) and with higher uric acid levels.

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6
Q

A 72-year-old woman presents with polyarticular joint pain. She has long-standing mild joint pain, but over the last 10 years notes increasing discomfort in her wrists, shoulders, knees, and ankles. She has had several recent episodes of severe pain in one or two joints, with swelling and warmth of the affected areas. These episodes often last 3-4 weeks. Her examination shows severe bony changes consistent with osteoarthritis in many joints, and slight swelling, warmth, and tenderness without erythema in the second and third metacarpophalangeal joints, left shoulder, and the right wrist.

A

psudogout (calcium pyrophosphate deposition)

Arthritis associated with CPP crystals is often called the great mimic and can have a wide variety of presentations.[1] Although the acute mono-articular arthritis resembling gout is perhaps the most commonly recognised form of CPP arthritis, it is not the most common form of the disease. The most common form of CPP arthritis presents as a chronic degenerative arthritis that resembles osteoarthritis and may occur with or without inflammatory episodes. CPP arthritis typically affects joints not commonly affected by osteoarthritis, such as the wrists or shoulders. In addition to its presentation as an acute mono-articular or oligo-articular arthritis, it can present with a polyarticular, symmetrical inflammatory arthritis similar to rheumatoid arthritis; or, less commonly, with the diffuse aching similar to that seen in polymyalgia rheumatica.

CPPD is associated with an increased risk of vascular calcification, and low bone mineral density.[5][6] The neuropathic form is rare but is characterised by severe destructive arthritis with bone fragmentation and loose bodies.

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7
Q

A 58-year-old woman presents with a 2-week history of fatigue, anorexia, fevers, and bilateral pain and stiffness in the shoulder and hip girdles. These symptoms are worse at night. Upon awakening in the morning, she feels as if she has a bad flu. She reports difficulty getting out of bed in the morning due to stiffness. Her wrists and finger joints are also painful and swollen.

A

polymyalgia rheumatica

Less common peripheral musculoskeletal manifestations include a monoarthritis or polyarthritis, pitting oedema of the hand, carpal tunnel syndrome, and tenosynovitis.[3] A second presentation is the presence of the characteristic neck, shoulder girdle, and hip girdle symptoms associated with normal serum markers of systemic inflammation (i.e., ESR or CRP).

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8
Q

A 72-year-old white woman presents with partial vision loss in the right eye. She reports bitemporal headache for several weeks, accompanied by pain and stiffness in the neck and shoulders. Review of systems is positive for low-grade fever, fatigue, and weight loss. On physical examination, there is tenderness of the scalp over the temporal areas and thickening of the temporal arteries. Fundoscopic examination reveals pallor of the right optic disc. Bilateral shoulder range of motion is limited and painful. There is no synovitis or tenderness of the peripheral joints. There are no carotid or subclavian bruits, and the blood pressure is normal and equal in both arms. The remainder of the examination is unremarkable.

A

GCA (giant cell arteritis)

When present, symptoms of jaw claudication and diplopia are powerful predictors of a positive temporal artery biopsy result.[1] Neurological manifestations occur in about one third of patients and may include stroke, transient ischaemic attack, or neuropathy. Respiratory tract symptoms are uncommon but may include cough or sore throat. Rarely, dental pain, tongue pain, or infarction of the tongue may be present. An older person may present with a new headache. In addition, some patients who predominantly have polymyalgia rheumatica can have subtle evidence of GCA that could be missed.[2] GCA can rarely present as an unexplained systemic illness or fever of unknown origin with elevated levels of inflammatory markers without headache, jaw claudication, shoulder or hip girdle stiffness, or visual disturbances.

Patients with large-vessel stenoses (approximately 10% to 15% of patients) may present with claudication of (usually) upper extremities, asymmetric blood pressures, or decreased pulses.[3] Rarely, involvement of lower extremity vessels results in leg claudication

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9
Q

A 38-year-old woman sees her physician with 4 years of widespread body pain. The pain began after a motor vehicle accident and was initially limited to her neck. Gradually, the pain has spread and she now complains of hurting all over, all the time. She does not have any joint swelling or systemic symptoms. She does not sleep well and has fatigue. She has irritable bowel syndrome but is otherwise healthy. Physical examination reveals a well-appearing woman with normal musculoskeletal examination, except for the presence of tenderness in 12 out of 18 fibromyalgia tender points. Routine laboratory testing is normal.

A

fibromyalgia

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10
Q

A 25-year-old man who is a known intravenous drug abuser presents with a 5-day history of pain and swelling in his right leg. On examination there are multiple sites of intravenous puncture. His right leg is swollen from the knee downwards. There is a large effusion on the right knee together with significant cellulitic changes of the overlying skin.

A

septic arthritis

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11
Q

A 63-year-old man with sun-damaged skin presents with a small nodule on the left aspect of his forehead. He mentions that it is itchy at times, and he thinks that he may have seen a colleague 2 years previously for removal of some keratoses or scabs. The patient indicates that these were either cauterised or frozen. On examination there is a pearly white nodule with prominent telangiectasia on its surface.

A

basal cell carcinoma

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12
Q

A woman in her mid-40s with dark, leathery skin and intense wrinkling of the lower neck (signifying excessive sun exposure either in a form of frequent sun tanning beds or perhaps frequent beach visits) presents at your office. She reports she has had multiple facial lifts, to decrease wrinkles. The plastic surgeon she has consulted performed other cosmetic procedures, including botulinum toxin type A injections. She complains about a mole on her jaw that has recently started to bleed.

A

basal cell carcinoma

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13
Q

A 21-year-old male student presents with a 4-week history of a painful, hot, and swollen left knee, low back pain with bilateral buttock pain, and left heel pain. He denies trauma and states the symptoms began acutely. He denies any fever or any other significant arthralgias. Further review of symptoms indicates the patient was treated for a chlamydia infection after he developed dysuria approximately 8 weeks ago (he was treated with a single dose of azithromycin). He admits to unprotected sexual intercourse with a new partner 2 days before the onset of his dysuria. In addition to pain and swelling, the patient reports that he has developed morning stiffness in the left knee and low back that last more than 1 hour. He continues to have episodes of dysuria. The findings of physical examination are significant for a large effusion of the left knee with warmth. Range of motion is slightly diminished. There is tenderness to palpation of the left heel at the site of the Achilles’ insertion. Laboratory findings are significant for an ESR of 35 mm/hour, and both FBC and uric acid level are within normal limits. He is HLA-B27 positive, rheumatoid factor negative, and ANA negative. The synovial fluid analysis is negative for crystals, with a total nucleated cell count of 22,000 cells/microlitre (65% neutrophils). A urethral swab was positive by PCR for Chlamydia trachomatis 9 weeks ago at initial presentation of dysuria. There was no evidence of gram-negative diplococci on Gram stain.

A

reactive arthritis

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14
Q

A 5-year-old boy fell off his bicycle 2 weeks ago and has stopped walking and complains of non-specific pain in his leg. His mother reports that he apparently has had flu, with fever and chills.

A

osteomyelitis

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15
Q

A 40-year-old man who suffered an open tibial fracture in a motor vehicle accident 6 months ago presents with swelling and pain in his lower leg.

A

osteomyelitis

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16
Q

A 52-year-old woman presents with a 2-month history of bilateral hand and wrist pain, and swelling in her fingers. She has also recently noted similar pain in the balls of her feet. She finds it hard to get going in the morning and feels stiff for hours after waking up. She also complains of increasing fatigue and is unable to turn on and off taps or use a keyboard at work without a significant amount of pain in her hands. She denies any infections before or since her symptoms started.

A

rheumatoid arthritis

RA can sometimes present in large joints like the knees and shoulders but this is less common. There is some evidence that elderly-onset RA may present this way more often.[3] Elderly-onset RA has also been grouped with polymyalgia rheumatica (PMR) and may represent a continuum of clinical features of both RA and PMR.[4] Rheumatoid nodules can be seen at presentation in some patients who have very active disease with large numbers of joints involved; these patients also have a higher incidence of rheumatoid vasculitis, presenting mostly as skin manifestations, with ulcerations and other rashes.

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17
Q

A 29-year-old woman presents with shortness of breath, cough, and painful red skin lesions on the anterior surface of the lower part of both legs. CXR reveals bilateral hilar lymphadenopathy with pulmonary infiltrates.

A

sarcoidosis

Multisystem involvement is characteristic, but pulmonary involvement usually dominates. Skin, eyes, and peripheral lymph nodes are involved in 15% to 30% of patients. Clinically significant involvement of spleen, liver, heart, CNS, bone, or kidney occurs in a few patients. Incidental diagnosis on routine CXR also occurs.

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18
Q

A 35-year-old woman presents with skin lesions around her nose, which are indurated plaques with discoloration. She also reports a red, moderately painful right eye with blurred vision and photophobia.

A

sarcoidosis

Multisystem involvement is characteristic, but pulmonary involvement usually dominates. Skin, eyes, and peripheral lymph nodes are involved in 15% to 30% of patients. Clinically significant involvement of spleen, liver, heart, CNS, bone, or kidney occurs in a few patients. Incidental diagnosis on routine CXR also occurs.

19
Q

A 45-year-old woman presents with fatigue and a history of positive ANAs. She has had recurrent sensation of sand/gravel in eyes and dry mouth every day for more than 3 months.

A

sjogren’s syndrome

Patients often present with non-specific fatigue or other rheumatological complaints such as joint pains, but upon questioning are also found to have dry eyes and mouth.

20
Q

A 38-year-old woman presents with Raynaud’s phenomenon for the past 5 years. She also has a history of digital ulcers and GORD. Physical examination reveals telangiectasias on the hands. She has sclerodactyly. Digital pits are present with no active ulcers. Serology tests reveal a high-titre ANA by indirect immunofluorescence, at a titre of >1:640 in a centromere pattern. The patient is diagnosed with limited cutaneous systemic sclerosis.

A

limited cutaneous systemic sclerosis

21
Q

A 35-year-old woman presents complaining of puffy hands and feet for the past 3 months. She noted the onset of Raynaud’s phenomenon 6 months ago. Examination confirms the presence of puffy hands and feet, with subtle skin thickening of the fingers and dorsum of the hands. Serology tests reveal a positive ANA with both speckled and nucleolar patterns at a titre of >1:1280. Anti-topoisomerase (anti-Scl 70) antibody is strongly positive. Pulmonary function tests are normal (although this does not preclude the possibility of the development of fibrosis at a later date). The patient is diagnosed with diffuse cutaneous systemic sclerosis.

A

diffuse cutaneous systemic sclerosis

22
Q

A 16-year-old black female presents to her general practitioner with symptoms of fatigue, musculoskeletal pain, and a facial rash. On examination she is noted to be thin with malar skin changes. No other abnormality is found.

A

SLE

23
Q

A 38-year-old white woman presents to the accident and emergency department with 24 hours of dyspnoea and pleuritic chest pain. On further questioning, she reports a 3-year history of Raynaud’s disease, polyarthralgia, and intermittent migraine. Physical examination reveals hypoxia, tachycardia, and normal blood pressure. Ventilation perfusion scanning confirms a pulmonary thromboembolism.

A

SLE

Most patients present with symptoms of fatigue, typical rash and/or musculoskeletal symptoms. Other symptoms and signs at presentation may include headaches or lymphadenopathy (cervical or axillary). Patients may present with pleuro- or pericarditis. Uncommon presentations include severe serositis or organ manifestations such as nephritis, possibly following triggers such as sun exposure or infection.

24
Q

A 50-year-old woman presents with numbness and tingling in her hands. The symptoms are worse in her right (dominant) hand and with activities such as holding a book or a steering wheel, or brushing her hair. The discomfort in her hands frequently wakes her at night, and she has to shake or hang her hand out of her bed for relief.

A

carpal tunnel syndrome

Pain or aching usually on the anterior aspect of the wrist (commonly in the region of the distal wrist crease), worse after activity or during the night. Aching often extends from the wrist to the forearm in many patients and to the upper arm in some. Clumsiness, loss of hand dexterity, and complaints of dropping things may be presenting features, mostly due to loss of afferent feedback from key functional fingers (first to third fingers in particular). There may be evidence of weakness and wasting in the hand, particularly over the thenar eminence.

25
Q

A 65-year-old male smoker with hypertension, dyslipidaemia, and diabetes mellitus presents with chest pain. ECG changes suggest an acute myocardial infarction. He is taken for an urgent coronary angiogram. Three days later, he is noticed to have developed an elevated serum creatinine, oliguria, and hyperkalaemia.

A

AKI

26
Q

A 48-year-old man has a 4-month history of increasing fatigue and anorexia. He has lost 5.5 kg and noticed increased skin pigmentation. He has been otherwise healthy. His mother has Hashimoto’s thyroiditis and one of his sisters has type 1 diabetes. His blood pressure is 110/85 mmHg (supine) and 92/60 mmHg (sitting). His face shows signs of wasting and his skin has diffuse hyperpigmentation, which is more pronounced in the oral mucosa, palmar creases, and knuckles.

A

addison’s disease

27
Q

A 60-year-old man presents with a 3-year history of diarrhoea, with no clear precipitating factors. Over the past few months he has noticed flushing affecting his face. These episodes occur at any time but are worse during times of stress and exercise. His wife has also noticed intermittent reddening of his face, which lasts for a few minutes. More recently he has not tolerated alcohol, chocolate, or bananas.

A

carcinoid syndrome

28
Q

A 50-year-old woman presents with a long history of atypical flushing, initially attributed to menopause. The flushing is associated with purplish discolouration of the face with each episode lasting 30 minutes. She also reports palpitations on exertion and recurrent episodes of abdominal pain.

A

carcinoid syndrome

Coincidental finding of liver metastases while other unrelated symptoms are being investigated is an alternative presentation. Other presentations include occasional abdominal pain, especially following large meals, and associated weight loss. Recurrent abdominal pain leading to development of sub-acute bowel obstruction can also occur. Patients can also present with cardiac signs, such as right heart failure and cardiac murmurs.

29
Q

A 34-year-old woman presents with complaints of weight gain and irregular menses for the last several years. She has gained 20 kg over the past 3 years and feels that most of the weight gain is in her abdomen and face. She notes bruising without significant trauma, difficulty rising from a chair, and proximal muscle wasting. She was diagnosed with type 2 diabetes and hypertension 1 year ago.

A

cushing’s

30
Q

A 54-year-old man presents for evaluation of an incidentally discovered adrenal nodule. He underwent a CT scan of the abdomen for evaluation of abdominal pain, which was negative except for a 2 cm well-circumscribed, low-density (2 Hounsfield units) nodule in the right adrenal gland. He reports weight gain of 15 kg over the past 4 years. He has difficult-to-control type 2 diabetes and hypertension. He has had 2 episodes of renal colic in the last 5 years.

A

cushing’s

31
Q

A 42-year-old man undergoes trans-sphenoidal surgery for a large, non-functioning pituitary macro-adenoma. Preoperatively, dynamic pituitary hormone tests were normal, as was his fluid intake and output. Two days following surgery he developed acute polyuria, extreme thirst, and polydipsia. His urine output over the next 24 hours was 6 litres, with frequent nocturia.

A

cranial DI

32
Q

A 75-year-old woman presents to her family physician with a 6-month history of progressive fatigue and malaise with polyuria, polydipsia, and nocturia. She has a long-standing history of bipolar affective disorder, and has been receiving lithium for the past 15 years.

A

nephrogenic DI

33
Q

A 25-year-old woman presenting with renal colic also complains of new-onset headaches, fatigue, and constipation. Her menstrual cycle is regular and she has not experienced episodes of flushing. Her weight is unchanged and her peripheral vision is normal. Family history reveals that her father had kidney stones and died of a ‘stomach problem’ in his 60s. Examination is unremarkable with visual fields full to confrontation.

A

multiple endocrine neoplasia syndrome

Presenting complaints can include any of the symptoms of any of the characteristic tumours.

Pituitary adenomas may present with headaches and visual field defects, or symptoms related to anterior pituitary hormone excess including galactorrhoea, low libido and oligo/amenorrhoea (due to a prolactinoma), sweating and increased ring/shoe size with or without diabetes mellitus (due to acromegaly), central adiposity, easy bruising, slow wound healing, emotional lability, proximal myopathy with or without hypertension and/or diabetes mellitus (due to Cushing’s disease), or symptoms of anterior pituitary hormone deficiency (due to a non-functioning pituitary adenoma).

Phaeochromocytomas may present with episodic headaches, sweating, palpitations, and hypertension.

Pancreatic lesions are often asymptomatic and may present with symptoms of peptic ulceration and diarrhoea (gastrinomas), recurrent hypoglycaemia (insulinomas), or diabetes with or without a rash (glucagonoma).

34
Q

An 18-year-old man with no medical history presents with a lump on his neck that he noticed while shaving. A 2-cm thyroid nodule is palpable. There is nothing else of note on examination.

A

multiple endocrine neoplasia syndrome

Presenting complaints can include any of the symptoms of any of the characteristic tumours.

Pituitary adenomas may present with headaches and visual field defects, or symptoms related to anterior pituitary hormone excess including galactorrhoea, low libido and oligo/amenorrhoea (due to a prolactinoma), sweating and increased ring/shoe size with or without diabetes mellitus (due to acromegaly), central adiposity, easy bruising, slow wound healing, emotional lability, proximal myopathy with or without hypertension and/or diabetes mellitus (due to Cushing’s disease), or symptoms of anterior pituitary hormone deficiency (due to a non-functioning pituitary adenoma).

Phaeochromocytomas may present with episodic headaches, sweating, palpitations, and hypertension.

Pancreatic lesions are often asymptomatic and may present with symptoms of peptic ulceration and diarrhoea (gastrinomas), recurrent hypoglycaemia (insulinomas), or diabetes with or without a rash (glucagonoma).

35
Q

A 33-year-old woman presents to her doctor complaining of a several-month history of episodic palpitations and diaphoresis. She states that her husband noticed that she becomes pale during these episodes. She has been experiencing progressive episodic headaches, which are not relieved by paracetamol. In the past, she has been told that she had a high calcium level. She has a history of kidney stones. Her family history is unremarkable; specifically, there is no history for tumours, endocrinopathies, or hypertension. Physical examination reveals a BP of 220/120 mmHg and hypertensive retinal changes.

A

phaeochromocytoma

A phaeochromocytoma may present in a patient with classic symptoms associated with excessive catecholamine secretion (i.e., diaphoresis, headaches, palpitations, and intractable and paroxysmal hypertension) or with a family history of phaeochromocytomas, or it may present as an incidental adrenal mass. However, the tumour can have an extremely variable presentation, making it a challenging diagnosis. Apart from the classic symptoms mentioned previously others include anxiety, epigastric pain, nausea, vomiting, and very rarely flushing.[3] Alternatively, the sole presenting complaint could be complications of intractable hypertension: for example, chest pain in a patient developing a myocardial infarction (MI). Due to the variety of hormones the tumour can produce, other unusual presentations may include Cushing syndrome from excess corticotrophin hormone or watery diarrhoea caused by excess vasoactive intestinal peptide (VIP) secretion.[6][7] Excessive catecholamine secretion may also lead to the development of new-onset diabetes and hyperglycaemia.[8][9] Increasingly, patients are asymptomatic, as these tumours are often diagnosed following work-up for an adrenal incidentaloma noted on imaging (CT scan, MRI).

36
Q

A 27-year-old woman presents with amenorrhoea. She had been taking the combined oral contraceptive pill for the last 9 years, stopping this 11 months ago. She is otherwise healthy, but on physical examination she has bilateral galactorrhoea. Laboratory work-up reveals an elevated prolactin level of 3000 mIU/L (150 micrograms/L). Normal prolactin levels are up to 500 mIU/L (25 micrograms/L). She also had low-normal gonadotrophin (luteinising hormone [LH], follicle-stimulating hormone [FSH]) levels. Magnetic resonance imaging (MRI) examination of the pituitary sellar region depicts a 6 mm right-sided pituitary mass, with no suprasellar or parasellar extension.

A

micro prolactinoma

37
Q

A 45-year-old man presents with loss of libido and some erectile dysfunction. He is otherwise healthy. On physical examination he has mild bilateral gynaecomastia and normal testes. Laboratory work-up reveals a highly elevated prolactin level of 46,000 mIU/L (2300 micrograms/L). Normal prolactin levels are up to 300 mIU/L (15 micrograms/L). He also has low testosterone, LH, and FSH levels. MRI examination of the pituitary sella depicts a large 32 mm pituitary macro-adenoma with suprasellar extension and optic chiasmal compression. Visual field assessment reveals bi-temporal hemianopia.

A

macro prolactinoma

38
Q

A 55-year-old man complains of persistently aching legs. He is initially diagnosed with fibromyalgia. However, his blood tests reveal an elevated serum alkaline phosphatase. Subsequent x-ray of the tibia and fibula shows defects in the cortical and cancellous bone, with some degree of tibial bowing, leading to a revised diagnosis of Paget’s disease.

A

paget’s disease of bone

39
Q

A late middle-aged woman presents with chronic right hip and anterior thigh pain, with increased localised temperature. Lately she has needed a walking stick. During the past 6 months her relatives have noticed a progressive hearing loss on her left side, as well as some facial changes - mostly enlargement of her mandible.

A

paget’s disease of bone

Paget’s disease is asymptomatic in most patients, and it is usually diagnosed by incidental findings on x-ray or elevated serum alkaline phosphatase.

Rarely, Paget’s disease is associated with the development of osteosarcoma, a malignant tumour of the bone. When there is a sudden onset or worsening of the chronic pain, osteosarcoma should be considered.

Paget’s disease affecting the facial bones may present with teeth becoming loose and associated chronic facial pain. Disturbance in chewing may occur. Osteoporosis, which shares the same age population, may occur concomitantly. Paget’s disease is only rarely encountered in the hands or feet.

40
Q

A 40-year-old man with a history of alcohol abuse is brought to the emergency department by police, who found him lying down by the side of the street. On examination he is somnolent and confused. He has a horizontal gaze palsy with impaired vestibulo-ocular reflexes and severe truncal ataxia in the presence of normal motor strength and muscle stretch reflexes.

A

wernicke’s encephalopathy

41
Q

A 30-year-old woman underwent bariatric surgery for morbid obesity. The postoperative course was complicated by a bronchopneumonia, vomiting, and poor oral intake. Four weeks after surgery she complained of vertigo and headache and soon became apathetic and developed vertical nystagmus that was worse on downward gaze.

A

wernicke’s encephalopathy

42
Q

A 68-year-old man with known coronary artery disease and peripheral vascular disease presents with recurrent episodes of flash pulmonary oedema, worsening kidney function, and progressively difficult-to-control hypertension. An angiogram of the aorta and renal arteries shows a sclerotic aorta with plaque extending into the proximal third of both renal arteries.

A

renal artery stenosis

43
Q

A 32-year-old woman with no prior medical history is seen for worsening headache and is found to have a BP of 180/110 mmHg. Her BP responds inadequately to thiazide diuretics and calcium-channel blockers. A magnetic resonance angiogram of the renal arteries reveals a beaded appearance indicative of fibromuscular dysplasia.

A

renal artery stenosis

44
Q

A 76-year-old homeless white man presents to the emergency department after police find him disoriented on the streets in late August. The patient gives little history, but admits to ongoing cough with productive sputum, night sweats/chills, and mild dyspnoea. He proceeds to suffer from a seizure. Vital signs demonstrate an elevated temperature at 38.7°C (101.7°F), a respiration rate of 26 breaths per minute, 94% oxygen saturation (on 3 L of O2), and pulse 87 bpm, with no evidence of orthostatic hypotension. Physical examination demonstrates a malnourished and dishevelled man in a postictal state. There is no sign of injury to the body. Crackles can be heard at the right lung base. Lab work demonstrates serum sodium of 120 mmol/L (120 mEq/L), serum creatinine of 88 micromol/L (1.0 mg/dL), and negative alcohol and toxicology screens. CXR demonstrates a large infiltrate in the right lower lung, consistent with pulmonary infection or abscess.

A

SIADH (although from this case you would need further tests to get this)