Valente A I, Pinto H C, Ramalho F, Cabrita P F, Catarino C, Serejo F, Baptista A, Saragoça A, Bordalo O, Moura M C
Department of Medicine 2, University Hospital of Santa Maria, Lisbon, Portugal.
Eur J Gastroenterol Hepatol. 1997 Aug;9(8):815-7. doi: 10.1097/00042737-199708000-00015.
We report the case of a 34-year-old white man with recurrent episodes of abdominal pain, cholestasis and eosinophilia. The diagnosis of idiopathic hypereosinophilic syndrome (IHS) was made after exclusion of all known causes of eosinophilia. Liver biopsy revealed an eosinophilic infiltrate with biliary damage. The patient recovered after prednisolone treatment. We review the literature on the association between IHS and liver disease.
我们报告了一例34岁白人男性，其反复出现腹痛、胆汁淤积和嗜酸性粒细胞增多。在排除所有已知的嗜酸性粒细胞增多原因后，诊断为特发性高嗜酸性粒细胞综合征（IHS）。肝脏活检显示嗜酸性粒细胞浸润伴胆汁损伤。患者经泼尼松龙治疗后康复。我们回顾了关于IHS与肝脏疾病关联的文献。
