J Korean Soc Endocrinol.  2002 Oct;17(5):730-738.

A Case of Papillary Thyroid Carcinoma Combined with Multiple Endocrine Neoplasia Type 2A

Affiliations
  • 1Department of Internal Medicine, National Health Insurance Corporation Ilsan Hospital, Korea.
  • 2Department of Surgery, National Health Insurance Corporation Ilsan Hospital, Korea.
  • 3Department of Pathology, National Health Insurance Corporation Ilsan Hospital, Korea.
  • 4Department of Internal Medicine, Yonsei University College of Medicine, Korea.
  • 5Familial Cancer Clinic, National Cancer Center, Korea.

Abstract

Multiple endocrine neoplasia (MEN) type 2A is a syndrome of medullary thyroid carcinomas, pheochromocytomas and parathyroid hyperplasia. The simultaneous occurrence of medullary, and papillary, thyroid carcinomas is rare because they are derived from, apparently, different germ layers, the former from the neuroectoderm and the latter from the endoderm. We report a case of a papillary thyroid carcinoma, combined with a medullary thyroid carcinoma, in a patient with MEN type 2A. Molecular genetic studies for screening a RET proto-oncogene mutation revealed a point mutation in codon 631 on chromosome 10, which is reported as highly uncommon in MEN type 2A.


MeSH Terms

Chromosomes, Human, Pair 10
Codon
Endoderm
Germ Layers
Humans
Hyperplasia
Male
Mass Screening
Molecular Biology
Multiple Endocrine Neoplasia Type 2a*
Multiple Endocrine Neoplasia*
Neural Plate
Pheochromocytoma
Point Mutation
Proto-Oncogenes
Thyroid Gland*
Thyroid Neoplasms*
Codon
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