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韩—薛—柯氏综合征(Hand—Schuller—Christian syndrome)是组织细胞增生症X(HistiocytosisX)中的一种类型,又称骨损害伴其它器官侵犯型。多发于幼儿,发病较慢。主要特征为颅骨缺损。突眼和尿崩。我们近见一例,临床症状典型,并经细胞病理学检查和X线摄片证实,现报告如下: 患儿刘××,男,3岁,因左眼突出、多饮多尿,于1981年11月入院。患儿在一年多前即开始左眼突出,不痛、不红,无任何不适。半年多来开始多饮、多尿,患儿常烦渴,每天要喝两水瓶水,小便约3000ml,夜间睡眠要起床小便2—3次,尿色清淡。
Hand-Schuller-Christian syndrome is a type of Histiocytosis X, also known as bone damage associated with other organ-invasive types. Occur in young children, the incidence is slower. The main feature is skull defects. Exophthalmos and insipidus. We recently saw a case of typical clinical symptoms, and confirmed by cytopathology and X-ray confirmed the report is as follows: Children Liu × ×, male, 3 years old, due to left eye prominent, polydipsi polyuria, in 1981 November admission. Children with left eye prominent more than a year ago, no pain, no red, no discomfort. More than six months began to drink more, more urine, children often polydipsia, drink two bottles of water a day, about 3000ml of urine, night sleep to get up 2-3 times urine, urine color light.