Pathology · Endocrine Pathology (Thyroid, Adrenal, Pituitary)

Multiple endocrine neoplasia type 2A (MEN2A) is caused by germline gain-of-function mutations in the RET proto-oncogene and includes medullary thyroid carcinoma (MTC), pheochromocytoma, and primary hyperparathyroidism. MTC arises from which thyroid cell type?

  • A Parafollicular C cells secreting calcitonin
  • B Follicular cells secreting thyroid hormone
  • C Sustentacular cells of the thyroid stroma
  • D Hurthle cell (oxyphilic) variant of follicular cells
Correct answer: A. Parafollicular C cells secreting calcitonin

Explanation

Medullary thyroid carcinoma arises from parafollicular C cells, which are neural crest-derived neuroendocrine cells that secrete calcitonin. Elevated serum calcitonin is the diagnostic tumor marker. Histologically, MTC shows amyloid stroma (calcitonin-derived AA amyloid) and stains positive for calcitonin and CEA. In MEN2A, RET Cys634 mutations are most frequent; in MEN2B, RET Met918Thr predominates.

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

High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP

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