Rare Tumors (Dec 2016)

Oncocytic variant of medullary thyroid carcinoma: a rare case of sporadic multifocal and bilateral RET wild-type neoplasm with revision of the literature

  • Gian Luca Rampioni Vinciguerra,
  • Niccolò Noccioli,
  • Claudia Cippitelli,
  • Angelo Minucci,
  • Ettore Capoluongo,
  • Armando Bartolazzi

DOI
https://doi.org/10.4081/rt.2016.6537
Journal volume & issue
Vol. 8, no. 4

Abstract

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Oncocytic variant of medullary thyroid carcinoma (OV-MTC) is a very unusual entity, up to date only 17 cases have been reported in the literature. MTC is a neuro-endocrine malignancy arising from the para-follicular C cells of the thyroid gland. It generally has a slight female predominance and appears as a single lesion. However in the Multiple Endocrine Neoplasia Syndrome 2, linked to the point mutation of RET oncogene, multifocal MTCs may also occur. Herein, we report the case of a 75 years old man with a rare form of sporadic multifocal and bilateral OV-MTC expressing wild-type RET gene. The histological and molecular features of this rare entity are presented and discussed with revision of the pertinent literature.

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