Vandewiele I A, Maeyaert B M, Van Cutsem E J, Geboes K R, Knockaert D C
Department of Internal Medicine, University Hospital Gasthuisberg, Leuven, Belgium.
Acta Clin Belg. 1991;46(1):37-41. doi: 10.1080/17843286.1991.11718139.
This paper describes a patient with massive eosinophilic ascites as presenting manifestation probably due to idiopathic hypereosinophilic syndrome. Eosinophilic ascites and stomach wall involvement were the first detected abnormalities. The subsequent course was characterised by interstitial pulmonary disease and pleural and pericardial effusion. Grand mal epilepsy and numbness of the left arm indicated central nervous system involvement. Treatment with corticosteroids resulted in complete remission. The differential diagnosis of eosinophilic gastroenteritis and idiopathic hypereosinophilic syndrome is discussed.
本文描述了一名以大量嗜酸性腹水为首发表现的患者,可能是由于特发性嗜酸性粒细胞增多综合征所致。嗜酸性腹水和胃壁受累是最早检测到的异常情况。随后的病程特点为间质性肺疾病以及胸腔和心包积液。癫痫大发作和左臂麻木提示中枢神经系统受累。使用皮质类固醇治疗后完全缓解。文中讨论了嗜酸性胃肠炎和特发性嗜酸性粒细胞增多综合征的鉴别诊断。