Congenital atrophic dermatofibrosarcoma protuberans
Congenital atrophic dermatofibrosarcoma protuberans
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先天性萎缩性隆突性皮肤纤维肉瘤
DOI：
10.1046/j.1365-4362.2001.01217.x
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发表时间：
2001
影响因子：
3.6
通讯作者：
Laura Remorino
中科院分区：
文献类型：
--
作者：
Mario Alberto Marini;A. Saponaro;G. Magariños;Alejandra De Baldrich;P. Lynch;Laura Remorino
一名16岁的女孩在其右腿前部出现先天性萎缩斑块。病变慢慢扩大，直到她9岁;随后，几个肿瘤出现在表面，后来变得发红，发热和轻微疼痛。 几个月内，所有的肿瘤都变平并消退。先前的活检显示为先天性纤维瘤。患者健康状况良好;体格检查、胸部X线片和实验室检查正常。没有记录个人或家族疾病史。
A 16‐year‐old girl presented with a congenital atrophic plaque on the anterior aspect of her right leg. The lesion had slowly enlarged until she was 9 years of age; subsequently, several tumors appeared on the surface and later became reddish, hot, and mildly painful. Within a few months, all the tumors flattened and involuted. A previous biopsy showed a congenital fibroma. The patient was in good health; the physical examination, chest X‐ray films, and laboratory studies were normal. No history of personal or familial diseases was recorded.