{"title":"儿童扩张型心肌病伴高免疫球蛋白E综合征1例","authors":"T. Alemayehu, E. Tefera","doi":"10.4314/EAMJ.V94I11","DOIUrl":null,"url":null,"abstract":"Hyper-immunoglobulin E syndrome is a rare primary immunodeficiency. We report a 6-year-old girl diagnosed with hyper immunoglobulin E syndrome and dilated cardiomyopathy. She presented with recurrent pneumonia and chronic eczema since infancy; onychomycosis, eosinophilia, high immunoglobulin E levels, previous treatment for severe infections and dilated cardiomyopathy. She was treated with diuretics, afterload reducers, inotropes, aspirin, steroids and antibiotics. Whether the cardiomyopathy is a co-incidental finding or a result of viral myocarditis due to the recurrent chest infections she had was difficult to conclusively determine.","PeriodicalId":11399,"journal":{"name":"East African medical journal","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Dilated cardiomyopathy in a child with hyper-immunoglobulin E syndrome\",\"authors\":\"T. Alemayehu, E. Tefera\",\"doi\":\"10.4314/EAMJ.V94I11\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Hyper-immunoglobulin E syndrome is a rare primary immunodeficiency. We report a 6-year-old girl diagnosed with hyper immunoglobulin E syndrome and dilated cardiomyopathy. She presented with recurrent pneumonia and chronic eczema since infancy; onychomycosis, eosinophilia, high immunoglobulin E levels, previous treatment for severe infections and dilated cardiomyopathy. She was treated with diuretics, afterload reducers, inotropes, aspirin, steroids and antibiotics. Whether the cardiomyopathy is a co-incidental finding or a result of viral myocarditis due to the recurrent chest infections she had was difficult to conclusively determine.\",\"PeriodicalId\":11399,\"journal\":{\"name\":\"East African medical journal\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"East African medical journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4314/EAMJ.V94I11\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"East African medical journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4314/EAMJ.V94I11","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
Dilated cardiomyopathy in a child with hyper-immunoglobulin E syndrome
Hyper-immunoglobulin E syndrome is a rare primary immunodeficiency. We report a 6-year-old girl diagnosed with hyper immunoglobulin E syndrome and dilated cardiomyopathy. She presented with recurrent pneumonia and chronic eczema since infancy; onychomycosis, eosinophilia, high immunoglobulin E levels, previous treatment for severe infections and dilated cardiomyopathy. She was treated with diuretics, afterload reducers, inotropes, aspirin, steroids and antibiotics. Whether the cardiomyopathy is a co-incidental finding or a result of viral myocarditis due to the recurrent chest infections she had was difficult to conclusively determine.
期刊介绍:
The East African Medical Journal is published every month. It is intended for publication of papers on original work and reviews of all aspects of medicine. Communications bearing on clinical and basic research on problems relevant to East Africa and other African countries will receive special attention. Papers submitted for publication are accepted only on the understanding they will not be published elsewhere without the permission of the Editor-in-Chief