✔ D

A perilymphatic fistula (choice D) between the middle and inner ear may be caused by barotrauma from scuba diving, as well as by direct blows, heavy weight-bearing, and excessive straining (e.g., with sneezing or bowel movements.) This patient's recent trip involved two of these potential factors. Most patients with fistulas find that their symptoms get worse with changes in altitude (elevators, airplanes, travel over mountain passes) or air pressure (weather changes).

⚠ Vestibular neuronitis (choice A) is a more sudden, unremitting syndrome.

⚠ Meniere's disease (choice B) is manifested by episodes of vertigo, associated with hearing loss and often with nausea and vomiting.

⚠ Benign paroxysmal positional vertigo (choice C) is more likely in older individuals and is associated with postural change.

⚠ Multiple sclerosis (choice E) requires symptoms in multiple areas and is not thought to be provoked by climate change.

🔖 Key point:

A perilymphatic fistula between the middle and inner ear may be caused by barotrauma from scuba diving, as well as by direct blows, heavy weight-bearing, and excessive straining. Most patients with fistulas find that their symptoms get worse with changes in altitude (e.g., elevators, airplanes, travel over mountain passes) or air pressure.

⚠ 🔔 𝐒𝐀𝐕𝐄 𝐓𝐇𝐈𝐒 𝐋𝐈𝐒𝐓 𝐅𝐎𝐑 𝐀 𝐑𝐀𝐈𝐍𝐘 𝐃𝐀𝐘 ! ⤵


1. 🧩 𝗠𝗘𝗗𝗜𝗖𝗔𝗟 𝗠𝗡𝗘𝗠𝗢𝗡𝗜𝗖𝗦 (𝗟𝗘𝗔𝗥𝗡 𝗘𝗔𝗦𝗜𝗟𝗬)

2. 𝗖𝗔𝗦𝗘 - 𝗕𝗔𝗦𝗘𝗗 𝗠𝗖𝗤𝗦 💯

3. 🇨🇦 𝗠𝗖𝗖𝗤𝗘 𝗣𝗥𝗘𝗣𝗔𝗥𝗔𝗧𝗜𝗢𝗡

4. 🩺 𝗘𝗗𝗟 𝗠𝗘𝗗𝗜𝗖𝗢𝗦 (𝗠𝗘𝗗𝗜𝗖𝗔𝗟 𝗕𝗢𝗢𝗞𝗦 𝗔𝗡𝗗 𝗟𝗜𝗡𝗞𝗦)

5. 📚 𝗘𝗗𝗟 𝗣𝗛𝗔𝗥𝗠

6. 🏛 𝗢𝗡𝗟𝗜𝗡𝗘 𝗠𝗘𝗗𝗜𝗖𝗔𝗟 𝗦𝗖𝗛𝗢𝗢𝗟

7. 𝗥𝗘𝗦𝗜𝗗𝗘𝗡𝗖𝗬 𝗜𝗡 𝗚𝗘𝗥𝗠𝗔𝗡𝗬 🇩🇪

8. 𝗣𝗥𝗔𝗖𝗧𝗜𝗖𝗘 𝗜𝗡 𝗔𝗨𝗦𝗧𝗥𝗔𝗟𝗜𝗔 🇦🇺

9. 𝗠𝗕𝗕𝗦 & 𝗥𝗘𝗦𝗜𝗗𝗘𝗡𝗖𝗬 𝗜𝗡 𝗜𝗧𝗔𝗟𝗬 🇮🇹

10. 𝗥𝗘𝗦𝗜𝗗𝗘𝗡𝗖𝗬 𝗜𝗡 𝗨𝗞 🇬🇧

11. 𝗥𝗘𝗦𝗜𝗗𝗘𝗡𝗖𝗬 𝗜𝗡 𝗨𝗦 🇺🇸

12. 𝗥𝗘𝗦𝗜𝗗𝗘𝗡𝗖𝗬 𝗜𝗡 𝗖𝗔𝗡𝗔𝗗𝗔 🇨🇦

13. 𝗙𝗥𝗘𝗡𝗖𝗛 𝗠𝗘𝗗𝗜𝗖𝗔𝗟 𝗕𝗢𝗢𝗞𝗦 🇫🇷

14. 𝗚𝗘𝗥𝗠𝗔𝗡 𝗠𝗘𝗗𝗜𝗖𝗔𝗟 𝗕𝗢𝗢𝗞𝗦 🇩🇪

15. 𝗠𝗘𝗗𝗜𝗖𝗔𝗟 𝗥𝗘𝗦𝗘𝗔𝗥𝗖𝗛 🎓

16. 📸 𝗗𝗘𝗥𝗠𝗔𝗧𝗢𝗟𝗢𝗚𝗬 𝗔𝗧𝗟𝗔𝗦

17. 𝗢𝗘𝗧 𝗣𝗥𝗘𝗣𝗔𝗥𝗔𝗧𝗜𝗢𝗡 🔡

18. 𝗠𝗘𝗗𝗜𝗖𝗔𝗟 𝗔𝗠𝗔𝗭𝗢𝗡 🌐

19. 𝗠𝗘𝗗𝗜𝗖𝗖𝗢𝗨𝗡𝗧 - 𝗠𝗘𝗗𝗜𝗖𝗔𝗟 𝗔𝗖𝗖𝗢𝗨𝗡𝗧

🧩 Medical Mnemonics

Learn Saccular Aneurysm Characters remembering the name of MASHA; A 22-year-old Iranian woman has died after being arrested by Iran's morality police earlier.

May Mahsa Amini rest in peace.🥀🖤

✌We stand for #Woman_Life_Freedom.

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#neurology
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©Medical Mnemonics

⏳ Case-based MCQ | #Case_465
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A 14-year-old girl is brought into the ED by her mother as she is worried about her daughter's weight. On history, she has lost 13.5 kg in the last six months and admits to fatigue, dry skin, hair loss, constipation, and poor concentration at school.

Upon hospital admission, the patient is started on nasogastric feeds to meet minimum caloric requirements. A few days after being admitted, the patient starts complaining of nausea, "stabbing" abdominal pain as well as vomiting without diarrhea. An abdominal radiograph shows a distended stomach but is otherwise normal.

✔ B

Superior mesenteric artery syndrome (SMA) (choice B) is the correct answer. This rare, but life-threatening condition must be considered in any patient with a history of rapid weight loss presenting with gastrointestinal symptoms. SMA syndrome describes the compression of the third portion of the duodenum by the abdominal aorta and the overlying superior mesenteric artery (see image below). Retroperitoneal fat and lymphatic tissue normally serve as a cushion for the duodenum, protecting it from compression by the SMA. This cushion effect is lost in cases of rapid weight loss. The resulting duodenal obstruction causes symptoms of epigastric pain (especially postprandial), nausea, vomiting, and early satiety. Abdominal CT scan is the modality of choice to make the diagnosis however signs of duodenal obstruction (gastric distension) may be present on radiographs.

⚠ Viral gastroenteritis (choice A) can have the described symptoms, but would typically be accompanied by lower GI tract symptoms as well (diarrhea). In addition, given this risk for SMA syndrome in this patient, a viral illness would be a diagnosis of exclusion.

⚠ While appendicitis (choice C) could be a possibility in any patient with nausea, vomiting and abdominal pain, the fact that she lacks fever and has a normal white count make it less likely. In addition, appendicitis would not explain the findings of stomach distension on the radiograph.  

⚠ Nutcracker syndrome (choice D) describes compression of the left renal vein between the aorta and the SMA. Symptoms are typically left flank pain and hematuria due to venous hypertension. This is an anatomical entrapment syndrome and, unlike SMA syndrome, is not related to sudden weight loss. 

⚠ Renal colic (choice E) typically presents with lower back/flank pain radiating to the groin. Most urinary calculi develop from the age of 20-40 (peak from 35-45 years), making it less likely in this adolescent.

🔖 Key point:

Superior mesenteric artery syndrome is rare, but life-threatening condition that must be considered in any patient with a history of rapid weight loss presenting with gastrointestinal symptoms. SMA syndrome describes the compression of the third portion of the duodenum by the abdominal aorta and the overlying superior mesenteric artery.

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The ratio of plasma aldosterone concentration to plasma renin activity is the preferred initial screening test for primary hyperaldosteronism.  Adrenal suppression testing can confirm the diagnosis, and positive tests require further adrenal imaging.  Adrenal venous sampling is the most sensitive test for differentiating adrenal adenoma and bilateral adrenal hyperplasia in patients without discrete unilateral adrenal mass on imaging.

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A 43-year-old man comes to the physician reporting acute-onset right knee pain.  He was diagnosed with diabetes mellitus a year ago and takes metformin.  He does not use tobacco, alcohol, or illicit drugs.  The patient is in a monogamous relationship.  His father also has diabetes.  His temperature is 37 C (98.6 F), blood pressure is 134/86 mm Hg, pulse is 86/min, and respirations are 16/min.  BMI is 26 kg/m2.  Physical examination shows a slightly swollen and tender right knee and mild hepatomegaly.  Right knee x-ray reveals chondrocalcinosis and a moderate effusion.  Appropriate analgesic is administered for joint pain.  Which of the following is the best next step in management of this patient?

A. Anticitrullinated peptide antibodies
B. Antismooth muscle antibodies
C. Liver biopsy
D. Serum iron studies
E. Serum uric acid level
F. Slit-lamp eye examination

Clinical manifestations of hereditary hemochromatosis

Skin

Hyperpigmentation (bronze diabetes)

Musculoskeletal

Arthralgia, arthropathy & chondrocalcinosis

Gastrointestinal

Elevated hepatic enzymes with hepatomegaly (early), cirrhosis (later) & increased risk of hepatocellular carcinoma

Endocrine

Diabetes mellitus, secondary hypogonadism & hypothyroidism

Cardiac

Restrictive or dilated cardiomyopathy & conduction abnormalities

Infections

Increased susceptibility to Listeria, Vibrio vulnificus & Yersinia enterocolitica

This patient has acute monoarticular arthritis with chondrocalcinosis (calcified articular cartilage on radiographs), diagnostic of calcium pyrophosphate dihydrate crystal deposition (CPPD) disease (pseudogout).  Patients with pseudogout should be evaluated for secondary causes such as hyperparathyroidism, hypothyroidism, and hemochromatosis.  Given this patient's recently diagnosed diabetes mellitus and hepatomegaly, hereditary hemochromatosis (HH) is highly likely.  HH-induced iron deposition in the synovial fluid appears to promote CPPD.  Diabetes in HH appears to be due primarily to loss of insulin secretion and often requires injectable insulin; however, mild or early disease is frequently managed with oral agents.

The initial evaluation of HH includes serum iron studies, which will show increased levels of serum iron, ferritin, and transferrin saturation.  The diagnosis can be confirmed with genetic testing for hemochromatosis-associated mutations (eg, HFE).  Liver biopsy is not required but may be useful to stage the extent of liver involvement (eg, in patients with significant liver function test abnormalities) or to confirm the diagnosis in patients who have iron studies indicating iron overload but negative results on the classic HFE gene markers (Choice C).  Long-term management of hemochromatosis involves serial phlebotomy to deplete excess iron stores.

(Choices A and E)  Chondrocalcinosis is not a typical feature of gout or rheumatoid arthritis (which is associated with anticitrullinated peptide antibodies).

(Choice B)  Antismooth muscle antibodies are seen in autoimmune hepatitis, which can be associated with other autoimmune disorders including type 1 diabetes mellitus, thyroid disease, and rheumatoid arthritis.  Patients may develop a subacute, symmetric polyarthritis involving the small joints, but acute monoarthritis with chondrocalcinosis would not be seen.

(Choice F)  Slit-lamp eye examination is helpful in identifying the Kayser-Fleischer rings of Wilson disease.  Wilson disease can cause hepatomegaly; however, it typically presents with neuropsychiatric manifestations, and almost all patients are diagnosed before age 35.

Educational objective:

Hereditary hemochromatosis is commonly associated with calcium pyrophosphate dihydrate crystal deposition in joints, leading to chondrocalcinosis, pseudogout, and chronic arthropathy.  Patients commonly also have diabetes and liver disease.  Diagnosis is suggested by iron overload on serum iron studies and can be confirmed by genetic tests

A 76-year-old woman comes to the office for evaluation of leukopenia.  The patient came to the United States to visit her son a month ago and was seen at an urgent care clinic 2 weeks ago for acute sinusitis, where she was found to have leukopenia.  She was prescribed an oral antibiotic, and a repeat blood test was advised.  The patient has had 2 episodes of skin infections over the past 3 months.  She also has had pain and swelling in the joints of her hands and knees for the past several years.  The patient does not use tobacco, alcohol, or illicit drugs.  Temperature is 37.2 C (98.9 F), blood pressure is 130/80 mm Hg, and pulse is 74/min.  Physical examination shows normal heart and lung sounds, moderate splenomegaly, generalized lymphadenopathy, no sinus tenderness, and well-healing lower extremity ulcerations.  The small joints of the hands are swollen and deformed.  Laboratory results are as follows:

Hemoglobin 11.8 g/dL
Mean corpuscular volume 92 µm3
Platelets 280,000/mm3
Leukocytes 1,800/mm3 (20% neutrophils)
Creatinine 0.8 mg/dL
Calcium 9.2 mg/dL
Erythrocyte sedimentation rate 68 mm/h
HIV serology negative
Additional evaluation of this patient is most likely to reveal which of the following?

A. Anticitrullinated peptide antibodies
B. Decreased vitamin B12 level
C. Hypocellular bone marrow
D. Philadelphia (Ph1) chromosome
E. Serum monoclonal proteins

Felty syndrome

⚪Clinical features

Rheumatoid arthritis
Severe erosive joint disease & deformity
Rheumatoid nodules
Vasculitis (mononeuritis multiplex, necrotizing skin lesions)
Neutropenia (ANC <2000/µL)
Splenomegaly

⚪Diagnosis

Anti-CCP & RF are positive in >90% of patients
Markedly elevated ESR, often >85 mm/hr
Peripheral smear & bone marrow biopsy to rule out other causes of neutropenia

ANC = absolute neutrophil count; anti-CCP = anticyclic citrullinated peptide; ESR = erythrocyte sedimentation rate; RF = rheumatoid factor.

This patient with swollen, deformed hand joints and an elevated erythrocyte sedimentation rate likely has untreated inflammatory polyarthritis.  The presence of concurrent neutropenia and splenomegaly raise strong suspicion for Felty syndrome, an uncommon but serious complication of long-standing, erosive rheumatoid arthritis (RA).

Felty syndrome is marked by the formation of autoantibodies against neutrophil components and granulocyte colony-stimulating factor, leading to neutropenia (ie, absolute neutrophil count <2,000/mm3) and an increased risk of recurrent bacterial infection (particularly of the skin and sinuses).  Neutrophils coated with antibodies are also trapped in the spleen, which usually results in splenomegaly.  Most patients also have extraarticular manifestations of RA such as lymphadenopathy, rheumatoid nodules, and/or necrotizing skin lesions.

The diagnosis is made based on clinical features but is supported by the presence of high-titer rheumatoid factor and anticitrullinated peptide antibodies (both of which are usually elevated in RA).  Most patients are also HLA-DR4 positive (indicating a genetic susceptibility).  Other causes of neutropenia should be ruled out with bone marrow biopsy and peripheral smear prior to establishing the diagnosis.  Symptoms generally improve with treatment of the underlying RA.

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🧩 Medical Mnemonics


Causes of delirium

🇮‌  ‌🇼‌‌🇦‌‌🇹‌‌🇨‌‌🇭‌    ‌🇩‌‌🇪‌‌🇦‌‌🇹‌‌🇭‌ ❗👽


🪧 🅘nfectious (encephalitis, meningitis, UTI)

🪧 🅦ithdrawal (alcohol, benzodiazepines)
🪧 🅐cute metabolic disorder (electrolyte imbalance)
🪧 🅣rauma (head injury, postoperative)
🪧 🅒NS pathology (stroke, hemorrhage, tumor)
🪧 🅗ypoxia (anemia, cardiac failure)

🪧 🅓eficiencies (vitamin B12, folic acid, thiamine)
🪧 🅔ndocrinopathies (thyroid, glucose)
🪧 🅐cute vascular (shock, vasculitis,
hypertension)
🪧 🅣oxins, substance use, medications
🪧 🅗eavy metals (arsenic, lead, mercury)

#psychiatry 
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©Medical Mnemonics