Which of the following is the most likely cause of this patient's current symptoms?
Anonymous Poll
20%
A. Clostridium perfringens infection
15%
B. Dietary noncompliance
10%
C. Pancreatic insufficiency
28%
D. Refractory celiac sprue
27%
E. Intestinal lymphoma
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This patient's presentation (3 months of fevers, abdominal pain, melena, and diarrhea) is concerning for intestinal lymphoma, specifically enteropathy-associated T cell lymphoma (EATL). This is a rare and aggressive lymphoma that is seen more commonly in celiac disease patients with poor dietary compliance. Patients present with abdominal pain, hepatosplenomegaly, ascites, duodenal masses, B symptoms (e.g., fever, night sweats, and weight loss), and gastrointestinal bleeding. Some patients may present with obstruction or perforation. The tumor is commonly located in the proximal jejunum and less frequently in the stomach, small bowel, or colon. A strict gluten-free diet also appears to reduce the incidence of EATL.
EATL should also be suspected in patients with refractory sprue despite good dietary compliance and failure of treatment with glucocorticoids. It may also be helpful to test for underlying celiac disease in all patients with a T cell lymphoma with or without gut involvement as celiac disease is undiagnosed in many individuals. However, EATL is uncommon in individuals diagnosed with celiac disease at a young age (< 33 years). Diagnosis is confirmed on pathology of resected tumor, which demonstrates multiple jejunal ulcers often with gut perforation. EATL has a poor prognosis and treatment consists of combination chemotherapy used for other aggressive T cell lymphomas.
Clostridium perfringens usually presents with self-limited watery diarrhea and enteritis necroticans (hemorrhagic necrosis of the jejunum), both of which would not cause symptoms for 3 months.
Poor patient compliance with a gluten-free diet is the most common cause of recurrence of bowel symptoms in celiac disease. However, poor compliance and disease recurrence usually do not cause persistent fever, as seen in this patient.
Patients with celiac disease may have coexisting pancreatic insufficiency. However, bloody stools and fever are not typically seen in chronic pancreatic insufficiency.
Refractory sprue is defined as persistent intestinal pathological changes despite a strict gluten-free diet for 12 months. However, this would not explain this patient's B symptoms or bloody diarrhea.
Enteropathy-associated T cell lymphoma is an aggressive lymphoma commonly seen in patients with celiac disease and poor dietary control. Patients present with abdominal pain, B symptoms, hepatosplenomegaly, ascites, bowel obstruction/perforation, and/or gastrointestinal bleeding. Diagnosis is confirmed by pathology of resected tumor. Prognosis is poor, and treatment involves combination chemotherapy.
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A 48-year-old woman presents to the clinic with dysphagia, diarrhea, and facial flushing. Physical examination reveals a solitary thyroid nodule and cervical lymphadenopathy. Laboratory studies show elevated serum calcitonin and elevated carcinoembryonic antigen levels.
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Which of the following is used to confirm the diagnosis of this patient?
Anonymous Poll
15%
A. Biochemical evaluation for pheochromocytoma
59%
B. Fine needle aspiration biopsy
11%
C. Germline RET mutation testing
14%
D. Ultrasonography of the neck
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The production of calcitonin and carcinoembryonic antigen (CEA) is characteristic of medullary thyroid cancer, and these are useful markers for diagnosis and follow-up. Patients typically present with dysphagia, diarrhea, facial flushing, and a solitary thyroid nodule. Medullary thyroid cancer is a neuroendocrine tumor of the parafollicular or C cells of the thyroid gland. The diagnosis of medullary thyroid cancer is made after a fine-needle aspiration biopsy of the thyroid nodule. Treatment is with the removal of the affected thyroid lobes, and for nodules that are 4 cm or larger, diagnostic lobectomy is recommended over fine-needle aspiration.
Although most cases of medullary thyroid cancer are acquired sporadically, genetic inheritance can be seen in cases of multiple endocrine neoplasia type 2 (MEN2). MEN2 is associated with medullary thyroid cancer, pheochromocytoma. and primary parathyroid hyperplasia. Therefore, additional testing for coexisting tumors such as biochemical evaluation for pheochromocytoma and germline RET mutation testing is recommended.
Once medullary thyroid cancer is confirmed with fine-needle aspiration biopsy, further evaluation should include ultrasonography of the neck to look for lymph node involvement.
Thyroid Carcinoma physical exam will show a solitary hard nodule. Labs will show normal thyroid function, cold nodule. Initial Diagnosis is ultrasound, and Confirmation is Fine-needle biopsy.
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A 34-year-old man is evaluated during a follow-up visit after passing his third calcium oxalate kidney stone in 4 years despite maintaining a high urine volume. He has no other medical problems. His only medication is potassium citrate, which was initiated after passing the most recent stone. He drinks 4 cups of coffee daily and typically eats meals at fast-food restaurants. Physical examination findings, including vital signs, are normal. Laboratory studies:
24-Hour urine studies
Volume 2600 mL
pH 6.5
Calcium 7.3 mmol (2.5–7.5)
Citrate 9 mmol (0.6–6.0)
Oxalate 0.35 mmol (0.44)
Uric acid 4.0 mmol (1.48–4.43)
The patient is counselled to start a low sodium diet.
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Which of the following is the most appropriate additional management?
Anonymous Poll
11%
A. Decrease calcium intake
30%
B. Decrease coffee intake
20%
C. Decrease oxalate intake
16%
D. Start allopurinol
22%
E. Start chlorthalidone
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This patient's urinary calcium excretion is in the high-normal range. The threshold that defines high urinary calcium excretion and when to initiate a thiazide diuretic for the prevention of calcium oxalate stones is unclear. However, the underlying principle is that the risk for stone formation is continuous with increasing amounts of calcium in the urine. Patients with ongoing stone formation despite dietary and fluid management should be considered for medical therapy with a thiazide diuretic to decrease urinary calcium excretion.
Thiazide diuretics can decrease calcium excretion by up to 50% and reduce the recurrence of calcium oxalate stones. Chlorthalidone is the preferred agent because of its long half-life. Chlorthalidone increases calcium reabsorption in the kidney primarily by causing mild volume depletion, which increases sodium and calcium reabsorption in the proximal tubule. When hydrochlorothiazide is used, twice-daily dosing is recommended. In addition to chlorthalidone, urinary calcium excretion can also be reduced by limiting sodium and protein intake.
Because calcium complexes with oxalate in the gastrointestinal tract, decreasing calcium intake allows for increased oxalate absorption and increased risk for stone formation. Therefore, unless a person is on a high-calcium diet (>1500 mg/d), intake should not be limited.
There is no evidence that excess coffee intake is associated with kidney stone disease, so reduction in coffee intake would not be expected to be beneficial.
Choice C is not correct:
Except in patients with hyperoxaluria, limiting oxalate intake has not been shown to decrease the incidence of stones, and thus the patient does not need to decrease intake.
Because uric acid may serve as a nidus for stone formation, allopurinol has been used to reduce stone occurrence, especially in patients with high levels of uric acid in the urine, which is not present in this patient.
Thiazide diuretics decrease calcium excretion by up to 50% and can be used to manage recurrent calcium oxalate kidney stones. In patients with recurrent calcium oxalate kidney stones, urinary calcium excretion can be reduced by limiting sodium and protein intake.
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A 58-year-old male presents to an emergency department complaining of severe knee pain which has been worsening over the past 2 days. He denies any trauma to the area. When questioned about his medical history, the patient reports that he is being treated for hypothyroidism. On examination, the patient has a temperature of 38 C (100.3 F). His left knee is warm, erythematous, and tender. There is a large effusion in the knee joint. He has painful limitation of motion of the knee. He has no rashes, and no other joints are involved. Arthrocentesis is performed and shows 75,000 WBC/mm3. A polarizing microscope shows rhomboid, positively birefringent crystals in the fluid.
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What is this patient’s diagnosis?
Anonymous Poll
41%
A. Pseudogout
20%
B. Gout
25%
C. Septic arthritis
10%
D. Rheumatoid arthritis
4%
E. Osteoarthritis
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Pseudogout is joint inflammation caused by calcium pyrophosphate crystals. it happens in Elderly and Osteoarthritis joint. Its Presentation is similar to gout cause redness, swelling, tenderness, but typically occurs in larger joints (knee).
Three main conditions that may increase crystal deposition include hemochromatosis, hyperparathyroidism, hypothyroidism (3 H’s).
The uric acid crystals of gout are needle-shaped and negatively birefringent.
This patient WBC count in the synovial fluid over 55.000 which suggest a septic arthritis, but the crystals point to pseudogout.
Rheumatoid arthritis is symmetrical arthritis and usually involve hands.
Osteoarthritis not come with fever, and synovial fluid WBC in osteoarthritis is less than 2000 and there is no crystal.
Fever and single joint pain next step is joint aspiration. Rhomboid crystal associated with Pseudogout. Risk factors for Pseudogout are hypothyroidism, Hemochromatosis, hyperparathyroidism. Pseudogout happen in Elderly and Osteoarthritis joint.
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A 68-year-old male presents to the emergency department with a complaint of right upper extremity weakness and slurred speech. His symptoms started 5 hours ago and have not improved. He has a medical history significant for hypertension and diabetes. His physical examination is notable for weakness in the right arm only and dysarthria, Right biceps reflex is brisk. The rest of the examination is normal. His temperature is 37.5, blood pressure is 190/100 mm Hg, the pulse is 75/min, respiratory rate is 12 /min.
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This patient has symptoms of an acute stroke. Strokes can be ischemic, caused by embolic events cutting cerebral blood flow, or hemorrhagic. CT scan of the head without contrast is the first best initial imaging study that needs to be ordered. This differentiates an ischemic from a hemorrhagic infarction.
Ischemic strokes appear as dark areas on the CT scan
Hemorrhagic strokes appear as white areas on the CT scan
MRI of brain is more sensitive than CT scan. Identifies all infarcts, and does so earlier than CT scan. 95% of infarcts identified on MRI within 24 hours. However, not preferred in an emergency setting because it is time consuming and is not suitable for potentially unstable patients.
First we need to identify with noncontract CT of head that patient has hemorrhagic or ischemic stroke. because they are contraindicated in the setting of a hemorrhagic stroke.
In all patient with suspicion of stroke first stabilize patient in primary survey doing ABC, Order labs like Noncontrast-CT scan of the brain, ECG, chest radiograph, CBC, platelet count, PT, PTT, Serum electrolytes, Glucose level, Bilateral carotid ultrasound and Echocardiogram. Noncontrast-CT scan will decide further treatment.
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A 4-year-old boy is brought to the physician for evaluation of a rash. The rash has been present for at least a month and became more prominent as the child spent more time playing outside during the summer. He has not used any new soaps, lotions, or detergents. Examination shows several hypopigmented macules on each cheek. Each macule is approximately 1 cm in diameter and is covered with a fine-scale. No other rashes or lesions are seen.
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Which of the following is the most appropriate treatment?
Anonymous Poll
8%
A. Diluted bleach water soaks weekly
16%
B. Oral ketoconazole daily
33%
C. Topical fluticasone daily
12%
D. Topical permethrin once a week
30%
E. Topical selenium sulfide daily
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Forwarded from Medical Mnemonics
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