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Arch Iran Med. 2015;18(5): 0.
PMID: 25959917
Scopus ID: 84928896788
  Abstract View: 2173
  PDF Download: 1426

Case Report

A Case of Familial Carney Complex

Yan-Li Zhang, Xiao-Cong Wang*, Wei Yu, Li-Ping Pei, Yan Ma, Shu Jiang, Yun-Peng Sun
*Corresponding Author: Email: 772431677@qq.com

Abstract

Carney complex is a syndrome characterized by skin pigmentation abnormalities, myxomas, endocrine tumors/overactivity, and schwannomas. It is caused by a mutation in the PRKAR1A gene that encodes the enzyme protein kinase A regulatory subunit type 1 alpha. A 23-year old male was diagnosed with Carney complex on the basis of spotty skin lentigines on his face and lips, multiple thyroid neoplasms, a right ventricular myxoma, and bilateral testicular tumors. A total bilateral orchectomy was performed and the pathological findings revealed Leydig's cell tumors on one side and a Sertoli cell tumor on the other side. When his first-degree relatives were examined, his mother was found to have Carney complex as well. This is the first reported case of familial Carney complex in China.

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ePublished: 01 May 2015
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