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Case Report of Rare Hereditary Endocrine Cancer Syndrome: Multiple Endocrine Neoplasia Type 2B

JOURNAL TITLE: Indian Journal of Endocrine Surgery and Research

Author

1. MJ Paul
2. Deepak Thomas Abraham
3. Varghese Thomas
4. Supriya Sen
5. Priyanka Rohit Singh
6. Shawn Sam Thomas
7. Shreya Surendra

ISSN

DOI

10.5005/jp-journals-10088-11188

Volume

Issue

Publishing Year

2022

Pages

Author Affiliations

Department of Endocrine Surgery, Christian Medical College, Vellore, Tamil Nadu, India

Department of Endocrine Surgery, Christian Medical College, Vellore, Tamil Nadu, India

Department of Endocrine Surgery, Christian Medical College, Vellore, Tamil Nadu, India
Christian Medical College, Vellore, Tamil Nadu, India

Medical College Hospital, Calicut, Kerala, India
Calicut Medical College
Government Medical College, Kozhikode, Kerala, India

Department of Endocrine Surgery, Christian Medical College, Vellore, Tamil Nadu, India

Department of Endocrine Surgery, Christian Medical College, Tamil Nadu, India

Department of Endocrine Surgery, CMC Hospital Vellore, Tamil Nadu, India, e-mail: mjpaul@cmcvellore.ac.in

Article keywords

Medullary thyroid carcinoma, Mucosal neuromas, Multiple endocrine neoplasia type 2B

Abstract

Abstract

Multiple endocrine neoplasia type 2B (MEN2B) is an extremely rare hereditary thyroid cancer syndrome. The individuals are presented with an aggressive form of medullary thyroid carcinoma (MTC). They have classic morphology features that aid in the diagnosis of the syndrome.