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A Case of Familial Carney Complex 期刊论文

编号：

93e0cb1b-49af-4963-9062-63e69b49cd97
作者：

Zhang, YanLi(张艳丽)#^[1]Wang, XiaoCong(王小丛)*^[1]Yu, Wei(于微)^[1]Pei, LiPing(裴莉平)^[1]Ma, Yan(马雁)^[1]Jiang, Shu^[1];Sun, YunPeng(孙云鹏)^[1]
语种：

英文
期刊：

ARCHIVES OF IRANIAN MEDICINE ISSN：1029-2977 2015 年 18 卷 5 期 (324 - 328) ; MAY
收录：
关键词：

Carney complex Leydig"s cell tumors myxomas PRKAR1A gene schwannomas Sertoli cell tumors skin lentigines
摘要：

Carney complex is a syndrome characterized by skin pigmentation abnormalities, mykomas, 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.
推荐引用方式
GB/T 7714：

Zhang Yan-Li,Wang Xiao-Cong,Yu Wei, et al. A Case of Familial Carney Complex [J].ARCHIVES OF IRANIAN MEDICINE,2015,18(5):324-328.
APA：

Zhang Yan-Li,Wang Xiao-Cong,Yu Wei,Pei Li-Ping,&Sun Yun-Peng.(2015).A Case of Familial Carney Complex .ARCHIVES OF IRANIAN MEDICINE,18(5):324-328.
MLA：

Zhang Yan-Li, et al. "A Case of Familial Carney Complex" .ARCHIVES OF IRANIAN MEDICINE 18,5(2015):324-328.
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