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Review Question - QID 100645

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QID 100645 (Type "100645" in App Search)
A 58-year-old female presents to her primary care physician with a 1-month history of facial and chest flushing, as well as intermittent diarrhea and occasional difficulty breathing. On physical exam, a new-onset systolic ejection murmur is auscultated and is loudest at the left second intercostal space. Subsequent echocardiography reveals leaflet thickening secondary to fibrous plaque deposition on both the pulmonic and tricuspid valves. Which of the following laboratory abnormalities would most likely in this patient?

Decreased serum chromogranin A

9%

12/132

Elevated serum bicarbonate

16%

21/132

Elevated urinary vanillylmandelic acid

23%

30/132

Elevated serum potassium

9%

12/132

Elevated urinary 5-hydroxyindoleacetic acid

35%

46/132

Select Answer to see Preferred Response

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This patient's presentation is consistent with a diagnosis of carcinoid syndrome. Elevated 24 hour urine levels of 5-hydroxyindoleacetic acid (5-HIAA) are diagnostic of carcinoid syndrome.

The GI tract is a common location for carcinoid tumors; however, carcinoid syndrome does not manifest until the tumor has metastasized to the liver or outside the GI tract, allowing for the released serotonin to escape hepatic degradation. Common presenting symptoms of carcinoid syndrome include flushing, diarrhea, tachycardia/hypotension, bronchospasm, telangiectasia, and right-sided heart failure. The right-sided heart disease of carcinoid syndrome involves endocardial plaques and fibrous intimal thickening, resulting in pulmonic stenosis, tricuspid insufficiency, and possibly restrictive cardiomyopathy.

Moerman et al. discuss the typical findings of carcinoid syndrome on echocardiography and cardiac MRI. Echo demonstrates thickening of leaflets and valvular insufficiency of both the tricuspid and pulmonic valves, ultimately leading to right heart failure. Cardiac MRI can visualize deposition of fibrous plaque on the walls of the right ventricle and can also be used to assess dilatation of the right ventricle.

Robertson et al. review the presentation, diagnosis, treatment, and prognosis of carcinoid tumors. Presentation of carcinoid tumors can be highly variable, ranging from asymptomatic to a more classic presentation, as in the above vignette. Carcinoid syndrome appears in only 10% of patients with carcinoid tumors and commonly does not present until the tumor has metastasized to the liver or lungs. Diagnosis centers around urine analysis for 5-HIAA, serum levels of Chromogranin A, radiographic imaging, and nuclear medicine scans targeting somatostatin receptors using radiolabeled octreotide.

Illustration A summarizes the clinical manifestations of carcinoid syndrome.
Illustration B depicts the right sided heart disease associated with carcinoid syndrome; note the deposition of plaques on the walls of the right ventricle, tricuspid insufficiency, and the stenosis of the pulmonic valve.

Incorrect Answers:
Answer 1: Carcinoid syndrome is associated with elevated levels of chromogranin A.
Answer 2: If the diarrhea associated with carcinoid syndrome was severe, metabolic acidosis (not alkalosis) would be expected due to loss of alkaline material.
Answer 3: Elevated urinary VMA would be expected in neuroblastoma or pheochromocytoma; VMA is a metabolite of epinephrine and norepinephrine.
Answer 4: If the diarrhea associated with carcinoid syndrome was severe, hypokalemia might be expected.

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