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麦格氏综合征以卵巢实质性肿瘤伴有胸水,腹水为特征。手术治疗预后良好。我们近年来遇到三例,其中两例来源子女性卵巢之功能性细胞瘤,另一例伴有肉眼血性胸腹水,病程短,肿瘤增长快,临床拟恶性卵巢肿瘤,经手术切除后,腹水、胸水消失,彻底治愈。现报道如下: 例一:张××,女性,53岁,住院号28832,因下腹部包块逐渐长大5个月伴腹胀、胸闷气急不能平卧两周,于1978年9月11日入院。以往月经正常,孕6产6,曾闭经8年。49岁月经复潮,近2个月月经紊乱,
Mackey’s syndrome is characterized by ovarian parenchymal tumor with pleural effusion and ascites. Surgical treatment of good prognosis. In recent years, we have encountered three cases, of which two cases originated from ovarian function of children’s tumors, the other case with gross bloody ascites, short course, rapid tumor growth, clinically malignant ovarian tumors, after surgical resection, ascites, Pleural effusion disappeared, completely cured. Now reported as follows: Example 1: Zhang × ×, female, 53 years old, hospitalization 28832, due to the lower abdomen mass gradually grew 5 months with abdominal distension, chest tightness, shortness of breath can not supine two weeks, admitted on September 11, 1978 . Normal menstruation in the past, 6 pregnant 6, had amenorrhea for 8 years. 49 years after the tide, nearly 2 months of menstrual disorders,