卵巢原发性恶性黑色素瘤伴麦格氏综合征罕见,我们遇一例,兹报告如下。患者鲍××,女,20岁。诉腹部逐渐增大伴隐痛3～4月。于1982年4月5日突感脐周与上腹部疼痛伴恶心、呕吐而拟诊为“胃炎”,经治疗未见好转,且腹部增大迅速伴发热、咳嗽.呼吸困难,不能平卧。于1982年4月30日入院。体检:呼吸急促,不能平卧。呼吸26次/分,脉搏90次/分,体温38.2℃。血压110/70mmHg,周身皮肤无色素痣。浅表淋巴结无肿大。心(-)。两肺下部叩诊呈实音,呼吸音明显减低,未闻啰音姓锒闲源┐坛榈糜倚厍坏粕禾逶?50ml,左胸腔淡黄色液体约60ml。腹部明显膨 Ovarian primary malignant melanoma with Magnus syndrome is rare. We have encountered one case and are hereby reported as follows. Patient Bao X, female, 20 years old. The v. abdomen gradually increases with pain from March to April. On April 5th, 1982, she was diagnosed with “gastritis” with pain in the umbilical cord and upper abdomen, accompanied by nausea and vomiting. The treatment did not improve, and her abdomen increased rapidly with fever and cough. Her breathing was difficult and she could not lie flat. He was admitted to hospital on April 30, 1982. Physical examination: shortness of breath, not lying. Breathing 26 beats/minute, pulse 90 beats/minute, body temperature 38.2°C. The blood pressure is 110/70mmHg, and the whole body has no pigmentation. Superficial lymph nodes are not swollen. heart(-). The lower lungs of the two lungs were diagnosed as real sounds, and the breath sounds were significantly reduced. No voice was heard, no name was found, and there was 50 ml of the left palm. The pale yellow liquid was about 60 ml in the left chest. Abdominal swelling