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肝脾的原发性血管肉瘤是极其罕見的,文献报导甚少。除嬰儿的肝脾血管內皮瘤外,国内仅見有江氏等(1957)报告一例脾脏原发性恶性血管瘤。本例为一尸检的脾肝血管肉瘤,肉瘤細胞进入骨髓及血液,并引起紅原細胞反应。今将本例略加整理,报导于后。
Primary splenic sarcoma of the liver and spleen is extremely rare, the literature reported little. In addition to the baby’s liver and spleen vascular endothelioma, the domestic only see Jiang et al (1957) reported a case of spleen primary malignant hemangioma. In this case an autopsy of splenic hepatic angiosarcoma, sarcoma cells into the bone marrow and blood, and cause erythroid cells response. This case a little finishing, reported later.