Denisov L E, Kudrina M I, Iarygin L M, Gribunov Iu P
Khirurgiia (Mosk). 1999(5):59-60.
Stewart-Treves Syndrome ('STS) is a rare, extremely malignant and quickly progressing tumor. It is angiosarcoma developing in lymphostasis of an arm after radical mastectomy for cancer. The patient aged 80 years was followed-up, in whom STS had developed 19 years after radical mastectomy. Clinical diagnosis was confirmed by pathomorphological examination of dermal biopsy. Advanced age and severe associated diseases made it impossible to carry out specific therapy. The patient died of intoxication and increasing cardio-vascular insufficiency 9 months after the onset of the disease.
斯图尔特-特里夫斯综合征('STS')是一种罕见、极具恶性且进展迅速的肿瘤。它是在乳腺癌根治术后手臂淋巴淤积处发生的血管肉瘤。对一名80岁患者进行了随访,该患者在乳腺癌根治术后19年发生了斯图尔特-特里夫斯综合征。通过皮肤活检的病理形态学检查证实了临床诊断。高龄和严重的相关疾病使得无法进行特异性治疗。患者在疾病发作9个月后死于中毒和日益加重的心血管功能不全。