论文部分内容阅读
脾原发性恶性肿瘤少见。我处1964年11月至1980年10月收治3例。报告于下:病例介绍例1 女15岁,住院号15201。二日前因上腹痛治疗缓解后发现腹块。伴有低烧,1964年5月29日以左上腹肿物收入院。一般情况中等,表浅淋巴结不大,胸部(一),左上腹部隆起可触及19×17×7cm 肿块,边界清楚,硬,表面不光滑。RBC301万,WBC12,450,血小板计数163,000,骨髓穿刺未见特殊异常。印象为脾血管瘤或淋巴肉瘤。
Splenic primary malignant tumors are rare. I was admitted to 3 cases from November 1964 to October 1980. Reported below: Case Introduction Case 1 Female, 15 years old, hospital number 15201. Abdominal mass was found after remission due to treatment of upper abdominal pain two days ago. Accompanied by low-grade fever, May 29, 1964 to the left upper abdominal mass was admitted to the hospital. Normal condition is moderate, superficial lymph nodes are not large, and the chest (1) and the left upper abdomen uplift can touch 19×17×7 cm masses with clear boundaries, hard and non-smooth surfaces. RBC 3.01 million, WBC12, 450, platelet count 163,000, no special abnormalities in bone marrow puncture. The impression is splenic hemangioma or lymphosarcoma.