Medicine · Diabetes Mellitus and Endocrine Disorders (Thyroid, Adrenal, Pituitary, Parathyroid)

A 9-year-old asymptomatic boy whose mother had medullary thyroid carcinoma is found to carry a germline RET proto-oncogene mutation. Basal calcitonin is elevated. What is the recommended surgical management?

  • A Total thyroidectomy with central compartment lymph node dissection
  • B Annual calcitonin surveillance with surgery once nodules appear
  • C Hemithyroidectomy followed by radioactive iodine ablation
  • D Total thyroidectomy with lateral neck dissection only if calcitonin exceeds 500 pg/mL
Correct answer: A. Total thyroidectomy with central compartment lymph node dissection

Explanation

Medullary thyroid carcinoma arises from parafollicular C cells, secretes calcitonin, and is not radioiodine avid, which eliminates options involving radioactive iodine. In a germline RET carrier, prophylactic total thyroidectomy with central lymph node dissection is performed in childhood because C-cell hyperplasia progresses to malignancy early, and waiting for nodules risks metastatic spread. Calcitonin is the tumor marker used for follow-up, not a trigger to defer surgery.

Reference: Robbins and Cotran Pathologic Basis of Disease, 10th ed.

High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP

Written and medically reviewed by the StethoPrep medical team.

Sponsored

Want to test yourself?

Create a free account for timed mock tests, mistake tracking, and FSRS spaced-repetition revision across 43,000+ MCQs.

Start free → Log in

More Diabetes Mellitus and Endocrine Disorders (Thyroid, Adrenal, Pituitary, Parathyroid) MCQs

See all Diabetes Mellitus and Endocrine Disorders (Thyroid, Adrenal, Pituitary, Parathyroid) MCQs →