wiskott—Aldrich综合症女性患者一例

• 作 者: 冯启高 吴元重 李世平
• 机 构: 蚌埠市第一人民医院,蚌埠市第一人民医院,蚌埠市第一人民医院,
• 出 处: 蚌埠医药
• 发表日期: 1987年02期
• 关键词: Aldrich wiskott 消化道出血 面黄 免疫缺陷病 女性病例 联合免疫缺陷 重度贫血貌 男性患儿 机会感染

Wiskott—Aldrich综合征(以下简称WAS)自1980年国内首次报道一例以来,已有18例相继被发表,但女性病例尚未见报导。我科于1986年收治一例女性患儿,现报导如下: 丁××,女,4岁。住院号86—388。因面黄、气喘、呕血、黑便十余天于86年1月25日入院。患儿终常发热、腹泻,生后2—3个月起面部及双下肢经常出现湿疹,痒感明显。近二年来因反复呕血、黑便先后三次在其他医院住院治疗,以“血小板减少症”、“消化道出血原因待查”诊断,给予相应处理,但效果不佳而转入我院。

Wiskott-Aldrich syndrome (hereinafter referred to as WAS) since the first report of a case in 1980, 18 cases have been published, but the female cases have not been reported. Our department admitted to a female child in 1986, is now reported as follows: Ding × ×, female, 4 years old. Hospital number 86-388. Due to face yellow, asthma, hematemesis, black stool more than ten days January 25, 1986 admission. Children with fever, diarrhea, 2-3 months after birth from the face and lower extremities often appear eczema, itching obvious. The past two years due to repeated hematemesis, black will have three other hospital treatment, with “thrombocytopenia”, “gastrointestinal bleeding due to be diagnosed,” given the appropriate treatment, but the results were poor and transferred to our hospital.