CHANG-MU CHENHONG-SHIEE LAILin C.-L.Hsieh K.-S.2020-03-162020-03-1619950022-3468https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028844967&doi=10.1016%2f0022-3468%2895%2990412-3&partnerID=40&md5=f96330d44306a972143eede4dff37914https://scholars.lib.ntu.edu.tw/handle/123456789/476299A Taiwanese boy was diagnosed as having hyperimmunoglobulin E syndrome at the age of 4 years. At age 18 he was admitted to the hospital because of pneumonia in the left lower lobe. Abdominal pain developed 9 days later, and his condition progressed to peritonitis. Colon perforation, 10 cm distal to the ileocecal valve, was found. Double-barrel ileostomy was performed, and reanastomosis was done 1 1 2months later. Afterward, he was fine, and he had no significant gastrointestinal problems after being discharged. To the authors' knowledge, this is the first reported case of hyperimmunoglobulin E syndrome complicated by colon perforation. ? 1995.[SDGs]SDG3ciprofloxacin; immunoglobulin e; adult; article; child; chronic granulomatous disease; clinical feature; colon perforation; echography; eczema; histopathology; human; human tissue; hyperimmunoglobulinemia e; ileostomy; laparotomy; lung abscess; male; medical record; pneumonia; priority journal; skin abscess; upper respiratory tract infection; Adolescent; Adult; Case Report; Child, Preschool; Colonic Diseases; Human; Intestinal Perforation; Job's Syndrome; Male; Staphylococcal Infectionsjournal article10.1016/0022-3468(95)90412-387864942-s2.0-0028844967