{"title":"高免疫球蛋白E综合征伴肾病综合征1例报告","authors":"S. Elfaituri","doi":"10.15406/JDC.2020.04.00168","DOIUrl":null,"url":null,"abstract":"A 3 years old child with coarse facial appearance was suffered from generalized eczema associated with secondary infections and recurrent multiple skin abscesses since he was 1 year old. The dermatitis and infections was present to some degree at all times. The patient had wheezy chest, food (cow milk) allergy and recurrent attacks of otitis media, candidiasis and herpes simplex virus infection with Kaposi varicelliform eruption. There was positive consanguinity between parents and positive family history with his older brother -5 years old, had similar disease. Routine blood counts revealed leukocytosis with persistent eosinophilia (40%).Blood chemistry was normal. The serum IgE level was11.000IU/ml with normal levels of other immunoglobulin classes.","PeriodicalId":23420,"journal":{"name":"Ukrainian Journal of Dermatology, Venerology, Cosmetology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Hyperimmunoglobulin E syndrome associated with nephrotic syndrome–case report\",\"authors\":\"S. Elfaituri\",\"doi\":\"10.15406/JDC.2020.04.00168\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A 3 years old child with coarse facial appearance was suffered from generalized eczema associated with secondary infections and recurrent multiple skin abscesses since he was 1 year old. The dermatitis and infections was present to some degree at all times. The patient had wheezy chest, food (cow milk) allergy and recurrent attacks of otitis media, candidiasis and herpes simplex virus infection with Kaposi varicelliform eruption. There was positive consanguinity between parents and positive family history with his older brother -5 years old, had similar disease. Routine blood counts revealed leukocytosis with persistent eosinophilia (40%).Blood chemistry was normal. The serum IgE level was11.000IU/ml with normal levels of other immunoglobulin classes.\",\"PeriodicalId\":23420,\"journal\":{\"name\":\"Ukrainian Journal of Dermatology, Venerology, Cosmetology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ukrainian Journal of Dermatology, Venerology, Cosmetology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15406/JDC.2020.04.00168\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ukrainian Journal of Dermatology, Venerology, Cosmetology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15406/JDC.2020.04.00168","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
一名面部粗糙的3岁儿童,自1岁起患有全身湿疹并继发感染和复发性多发性皮肤脓肿。皮炎和感染在任何时候都不同程度地存在。患者有胸鸣、食物(牛奶)过敏,中耳炎、念珠菌病、单纯疱疹病毒感染反复发作,伴卡波济水痘样疹。父母间有阳性血缘关系,与哥哥-5岁,有类似疾病,家族史阳性。常规血球计数显示白细胞增多伴持续性嗜酸性粒细胞增多(40%)。血液化学正常。血清IgE水平为11.000 iu /ml,其他免疫球蛋白类正常。
Hyperimmunoglobulin E syndrome associated with nephrotic syndrome–case report
A 3 years old child with coarse facial appearance was suffered from generalized eczema associated with secondary infections and recurrent multiple skin abscesses since he was 1 year old. The dermatitis and infections was present to some degree at all times. The patient had wheezy chest, food (cow milk) allergy and recurrent attacks of otitis media, candidiasis and herpes simplex virus infection with Kaposi varicelliform eruption. There was positive consanguinity between parents and positive family history with his older brother -5 years old, had similar disease. Routine blood counts revealed leukocytosis with persistent eosinophilia (40%).Blood chemistry was normal. The serum IgE level was11.000IU/ml with normal levels of other immunoglobulin classes.