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尼曼-匹克氏病(Nieman-Pick’s disease)为一罕见的先天性家族性疾病。本病可分为婴幼型与成年型二种,前者较多见。现将遇到的1例报告于下。兰××,女性,21岁,农民,住院号13077。患者以反复鼻衄5年、左上腹痞块3个月为主诉入院。患者于入院前5年发现脸色逐渐苍白,体力不断下降,且常发生鼻衄,时有皮肤紫癜及左上腹闷痛。入院前3个
Nieman-Pick’s disease is a rare, congenital familial disease. The disease can be divided into two types of infant and adult type, the former more common. Now encountered in 1 case reported below. Lan × ×, female, 21 years old, farmer, hospital number 13077. Patients with repeated epistaxis 5 years, the left upper quadrant lumbar lumps for 3 months based on admission. 5 years before admission, patients found his face gradually pale, physical decline, and often occur epistaxis, purpura and left skin when there was pain in the left upper quadrant. 3 before admission