Santos J, Junquera F, de Torres I, Molero X, Vilaseca J, Malagelada J R
Digestive System Research Unit, Hospital General Vall d'Hebron, Autonomous University of Barcelona, Spain.
Eur J Gastroenterol Hepatol. 1995 Jul;7(7):675-8.
A 25-year-old man with a 1 year history of episodic abdominal pain presented with splenomegaly, eosinophilic ascites and peripheral eosinophilia. Full-thickness biopsies from his gastrointestinal tract revealed intense eosinophilic infiltration involving both muscular and serosal layers and extending from his stomach to his ileum. When given oral steroids, the patient's condition improved and he was discharged without symptoms. Eighteen months later, he remains asymptomatic and without recurrence of ascites or splenomegaly. This report adds to the scarce data on extraintestinal involvement in eosinophilic gastroenteritis. Special attention is drawn to the differential diagnosis of eosinophilic ascites and to the optimal approach to its management.
一名有1年发作性腹痛病史的25岁男性,出现脾肿大、嗜酸性粒细胞性腹水和外周血嗜酸性粒细胞增多。来自其胃肠道的全层活检显示,嗜酸性粒细胞强烈浸润,累及肌层和浆膜层,从胃延伸至回肠。给予口服类固醇后,患者病情改善,无症状出院。18个月后,他仍无症状,腹水和脾肿大未复发。本报告增加了关于嗜酸性粒细胞性胃肠炎肠外受累的稀少数据。特别关注嗜酸性粒细胞性腹水的鉴别诊断及其最佳管理方法。