Al'pidovskiĭ V K, Suvorova E V, Halil M A
Ter Arkh. 1990;62(9):124-6.
A female patient with intravitally diagnosed splenic angiosarcoma is described. Progress of the cancerous process was attended by the development of consumption coagulopathy with profound fibrinogenopenia and thrombocytopenia. In this case the DIC syndrome was characterized by the lack of systemic fibrinolysis activation. The rupture of the cavernous tumor of the spleen and profound disorders of hemostasis determined profuse intraperitoneal hemorrhage and the patient's death. Diagnostic criteria that contribute to early recognition of splenic angiosarcoma are suggested.
本文描述了一名经活体诊断为脾血管肉瘤的女性患者。癌症进展过程中出现了消耗性凝血病,伴有严重的纤维蛋白原减少和血小板减少。在该病例中,弥散性血管内凝血(DIC)综合征的特征是缺乏全身性纤维蛋白溶解激活。脾海绵状肿瘤破裂及严重的止血障碍导致了大量腹腔内出血,最终患者死亡。文中还提出了有助于早期识别脾血管肉瘤的诊断标准。