医学
骨肉瘤
软骨肉瘤
病理
皮肤病科
沃纳综合征
生物
基因
生物化学
核糖核酸
解旋酶
作者
Kaoru Murata,Atsushi Hatamochi,Hiroshi Shinkai,Yuichi Ishikawa,Noriyoshi Kawaguchi,Makoto Goto
标识
DOI:10.1111/j.1346-8138.1999.tb02072.x
摘要
Abstract We described a case of Werner's syndrome associated with osteosarcoma. A 37‐year‐old Japanese man was diagnosed as having Werner's syndrome by the presence of juvenile cataracts, skin sclerosis and hyperpigmentation of the feet, high‐pitched voice, characteristic bird‐like appearance of the face with beak‐shaped nose, thinning of the entire skin and hyperkeratoses on soles, hyperlipemia, hyperuricemia, diabetes melitus, and the mutated responsible gene (WRN). He had a 3‐month history of a tumor on his left forearm. Histologically, the tumor included four histological patterns; a malignant fibrous histiocytoma‐like, a desmoid‐like, a dermatofibrosarcoma protuberans‐like, and a chondrosarcoma‐like pattern. Tumoral osteoid formation was also found in the tumor. Therefore, the tumor was diagnosed as osteosarcoma.
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