Gardner fibroma with localized hypertrichosis without adenomatous polyposis coli gene mutation  

作　　者：Xue-Yan Yao Guang-Dong Wen Dong-Dong Che Dan-Hua Shen Jiang-Zhong Zhang Cheng Zhou 

机构地区：[1]Department of Dermatology, Peking University People’s Hospital, Beijing 100044, China [2]Department of Ultrasound, Peking University People’s Hospital, Beijing 100044, China [3]Department of Pathology, Peking University People’s Hospital, Beijing 100044, China

出　　处：《Chinese Medical Journal》2019年第17期2129-2130,共2页中华医学杂志（英文版）

基　　金：This work was supported by grants from the National Natural Science Foundation of China (No. 81402588 and 81773311).

摘　　要：To the Editor: Gardner fibroma (GAF)[1] is usually companied by familial adenomatous polyposis (FAP), which is related to mutations in adenomatous polyposis coli (APC).[2,3,4] Both GAF and FAP present with signs of Gardner syndrome (GS), triad of intestinal polyposis, soft tissue tumor (including GAF and desmoid), and osteomas.[2,3,4] Here, we presented a man who was diagnosed with sporadic GAF without APC gene mutations. In addition, a tubular adenoma was revealed in his sigmoid.

关 键 词：FIBROMA DESMOID adenomatous 

分 类 号：R[医药卫生]