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General Surgery · Thyroid: MEN2 prophylaxis
Sample itemA 3-year-old child is found by family screening to carry a RET codon 634 mutation (MEN2A). Calcitonin is normal and the neck is clinically normal. What is the recommended management of the thyroid?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
C. Prophylactic total thyroidectomy at or before 5 years of age
Medullary thyroid carcinoma develops in virtually all RET carriers, and the age of onset correlates with the codon. For codon 634 (high-risk), total thyroidectomy is advised at or before age 5, guided by calcitonin, while codon 918 (highest-risk) mutations need surgery in the first year of life. Phaeochromocytoma is screened for before any surgery.
Option by option
A. Bilateral adrenalectomy first
The adrenal is not the first priority, since prophylactic thyroid surgery is driven by medullary carcinoma risk.
B. Waiting until a thyroid nodule appears
Waiting for a nodule risks metastatic disease, because spread can precede a palpable lump.
C. Prophylactic total thyroidectomy at or before 5 years of age (correct)
Correct. Early prophylactic total thyroidectomy prevents or cures the medullary carcinoma.
D. Annual ultrasound only until adulthood
Surveillance alone does not remove the near-certain risk of carcinoma.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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