Histopathologic and clinical features of medullary microcarcinoma and C-cell hyperplasia in prophylactic thyroidectomies for medullary carcinoma: a study of 42 cases

Arch Pathol Lab Med. 2008 Nov;132(11):1767-73. doi: 10.5858/132.11.1767.

Abstract

Context: Prophylactic thyroidectomies are increasingly performed on patients at risk for developing medullary thyroid carcinoma (MTC); consequently, pathologists are more commonly encountering these specimens in routine practice.

Objective: To describe the detailed clinicopathologic features of prophylactic thyroidectomies for medullary carcinoma.

Design: We present a retrospective series of 42 prophylactic thyroidectomies for MTC performed for one or more of the following: family history of multiple endocrine neoplasia (MEN) or MTC, elevated serum calcitonin level, or detection of a RET proto-oncogene mutation.

Results: Patients included 22 men and 20 women (mean age, 26.2 years). Among those with known RET proto-oncogene mutations, affected sites included exons 10, 11, 14, and 16. In 93% (n = 39) of cases, either C-cell hyperplasia (n = 36), medullary microcarcinoma (MMC; n = 29), or medullary macrocarcinoma (n = 1) was found. C-cell hyperplasia was often multifocal (n = 30) and bilateral (n = 23) and included both nonnodular and nodular patterns. A total of 94% of C-cell hyperplasia cases and all MMC cases were microscopically detectable using hematoxylin-eosin stains. The MMCs were characterized by a complex microarchitectural pattern with a desmoplastic stromal response (n = 29) and focal amyloid deposition (n = 12). Most MMCs exhibited a solid pattern (n = 24) of round, polygonal, spindled, or plasmacytoid-shaped cells. Only 1 case of MMC showed evidence of metastatic disease to a pretracheal lymph node.

Conclusions: Based upon our clinicopathologic findings and review of the literature, we conclude that thyroidectomies in at-risk patients are very frequently associated with C-cell hyperplasia and/or MMC; however, the clinical prognosis for these patients is very good.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Calcitonin / blood
  • Carcinoma, Medullary / pathology*
  • Carcinoma, Medullary / prevention & control*
  • Carcinoma, Medullary / surgery
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Hyperplasia / pathology
  • Lymph Nodes / pathology
  • Male
  • Middle Aged
  • Mutation / genetics
  • Parathyroid Glands / pathology
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins c-ret / genetics
  • Retrospective Studies
  • Thyroid Gland / pathology*
  • Thyroid Gland / surgery
  • Thyroid Neoplasms / pathology*
  • Thyroid Neoplasms / prevention & control*
  • Thyroid Neoplasms / surgery
  • Thyroidectomy

Substances

  • MAS1 protein, human
  • Proto-Oncogene Mas
  • Calcitonin
  • Proto-Oncogene Proteins c-ret