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* Năm 2019 - Tập 23 - Số 4
BÁNG BỤNG: MỘT ĐẶC ĐIỂM HIẾM GẶP DO VIÊM DẠ DÀY RUỘT TĂNG BẠCH CẦU ÁI TOAN TẠI BỆNH VIỆN NHI ĐỒNG 2: BÁO CÁO TRƯỜNG HỢP

Hà Văn Thiệu*, Nguyễn Minh Ngọc*, Ngô Văn Bách*, Vũ Bảo Sơn*

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Ha Van Thieu, Nguyen Minh Ngoc, Ngo Van Bach, Vu Bao Son
* Ho Chi Minh City Journal of Medicine * Supplement of Vol. 23 – No. 4 - 2019: 55 – 59

Eosinophilic gastroenteritis (EGE) is a rare disease of unknown etiology. It is characterized by eosinophilic infiltration of the gastrointestinal (GI) tract and elevated peripheral eosinophilia. This disease was first described by Kajiser in 1937. The prevalence of EGE in the United States estimated to be 22 to 28 per 100,000 persons. The clinical manifestations vary and a number of tests may aid in the diagnosis of EGE as there are no standards for diagnosis. Diagnosis of EGE requires three criterias: presence of GI symptoms, histologic evidence of eosinophilic infiltration in one or more areas of the GI tract and exclusion of other causes of tissue eosinophilia. Ascites due to EGE is an exceedingly uncommon diagnosis in the medical literature. Here, we present a rare case of EGE with ascites and discuss the clinical characteristics and differential diagnosis. The management and follow up plan still needs more consensus because it almost depends on an elemental formula and steroids. We reported EGE in a child admitted to Childrens Hopital 2 from 04/2018 to 06/2018.

Keywords: eosinophilic gastroenteritisin children

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