Hwang E H, Oh J T, Han S J, Kim H
Department of Pediatric Surgery and Pathology, Yonsei University College of Medicine, Seoul, Korea.
J Pediatr Surg. 1998 Sep;33(9):1420-2. doi: 10.1016/s0022-3468(98)90025-2.
Colon perforation from hyperimmunoglobulin E syndrome is very rare, and only one case has been reported in the English-language literature. Herein, the authors report another case of colon perforation experienced in hyperimmunoglobulin E syndrome. The patient was an 8-year-old girl with frequent infection, eczematoid dermatitis, and an increased serum level of immunoglobulin E. During admission, panperitonitis developed caused by colon perforation. Treatment was resection of the perforated segment of the colon and a double-barrel colostomy. The patient has been doing well 18 months after treatment.
高免疫球蛋白E综合征导致的结肠穿孔非常罕见，英文文献中仅报道过一例。在此，作者报告了另一例高免疫球蛋白E综合征患者发生结肠穿孔的病例。该患者为一名8岁女童，有频繁感染、湿疹样皮炎，血清免疫球蛋白E水平升高。入院期间，因结肠穿孔发展为弥漫性腹膜炎。治疗方法是切除结肠穿孔段并进行双腔结肠造口术。治疗后18个月，患者情况良好。
