[斯图尔特-特雷夫斯综合征]
[Stewart-Treves syndrome].
作者信息
Pirard C, Bourlond A
出版信息
Dermatologica. 1985;170(6):286-92.
PMID:4018337
Abstract
A Stewart-Treves angiosarcoma (Stewart-Treves syndrome) developed 14 years after mastectomy (Halsted) and radiotherapy for breast cancer in a woman now 56 years old. Limited excision, graft and complementary radiotherapy have controlled the disease for 20 months. The microscopical and ultrastructural features of this angiosarcoma are presented and the last advances in immunopathology briefly commented.
摘要
一名56岁女性在接受乳腺癌根治术（霍尔斯特德术式）及放疗14年后发生了斯图尔特-特里夫斯血管肉瘤（斯图尔特-特里夫斯综合征）。有限切除、植皮及辅助放疗已使病情得到控制达20个月。本文展示了该血管肉瘤的显微镜及超微结构特征，并简要评述了免疫病理学的最新进展。
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