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盲肠原发性恶性纤维组织细胞瘤临床上较少见。患者,男,47岁,近一年来右下腹间歇性隐痛,入院前一日右下腹痛加剧,放射到会阴部疼痛,伴发烧,无呕吐,无明显过敏史,于1983年1月20日入院。体检:体温39.5℃,脉博90次,血压120/80,发育正常,贫血貌,巩膜无黄染,表浅淋巴结无肿大,心肺正常,腹部稍有膨胀,可见肠形及蠕动波,右下腹压痛,反跳痛,未触及包块,肝脾不肿大,无腹水征,肠鸣音亢进,肛门指检无血
Primary cecal malignant fibrous histiocytoma is rare in clinical practice. Patient, male, 47 years old, had intermittent pain in the right lower abdomen for the past year, aggravated right lower abdominal pain on the day before hospital admission, pain radiating to the perineum, fever, no vomiting, and no history of allergies. She was admitted to hospital on January 20, 1983. . Physical examination: body temperature 39.5 °C, pulse 90 times, blood pressure 120/80, normal development, anemia appearance, sclera without yellow stain, superficial lymph nodes without enlargement, normal heart and lung, abdominal slightly expanded, visible intestinal and peristaltic waves, right Lower abdominal tenderness, rebound tenderness, untouched mass, no hepatosplenomegaly, no ascites, hyperactive bowel sounds, no anal blood test