Talley N J, Shorter R G, Phillips S F, Zinsmeister A R
Department of Pathology, Mayo Clinic, Rochester, MN 55905.
Gut. 1990 Jan;31(1):54-8. doi: 10.1136/gut.31.1.54.
The aim of this study was to evaluate the clinicopathological spectrum of eosinophilic gastroenteritis and identify possible difficulties in establishing the diagnosis. All patients with a diagnosis of eosinophilic gastroenteritis, defined by the presence of gastrointestinal symptoms and eosinophilic infiltration of the gut (38), or a radiological diagnosis with peripheral eosinophilia (two), were identified from the Mayo Clinic records; in none was there evidence of extraintestinal disease. Patients were divided into three groups according to the Klein classification: predominant mucosal (23), muscular (12), or subserosal disease (five). A fourth group of patients (10) for comparison had abdominal symptoms and unexplained peripheral eosinophilia but no proven eosinophilic infiltration of the gut. It was found that a history of allergy was reported by 20 of 40 patients with eosinophilic gastroenteritis. Peripheral eosinophilia was absent in nine of 40. The patients with subserosal disease were distinct from the other groups in presentation (abdominal bloating, ascites), higher eosinophil counts and in their dramatic responses to steroid therapy. Otherwise the patients were similar regarding demographic factors, presenting symptoms (abdominal pain, nausea, weight loss, diarrhoea), and laboratory parameters. The ESR was moderately raised in 10 of 40 patients. The disease may affect any area of the gastrointestinal tract; eosinophilic infiltration was documented in the oesophagus in one patient and in the colon in two cases. Endoscopic biopsies missed the diagnosis in five of 40 presumably because of patchy disease. Eosinophilic gastroenteritis should be considered in the differential diagnosis of unexplained gastrointestinal symptoms even in the absence of peripheral eosinophilia.
本研究的目的是评估嗜酸性粒细胞性胃肠炎的临床病理谱,并确定在建立诊断时可能遇到的困难。从梅奥诊所的记录中识别出所有诊断为嗜酸性粒细胞性胃肠炎的患者,其定义为存在胃肠道症状且肠道有嗜酸性粒细胞浸润(38例),或经放射学诊断且外周血嗜酸性粒细胞增多(2例);所有患者均无肠道外疾病的证据。根据克莱因分类法,将患者分为三组:主要为黏膜型(23例)、肌层型(12例)或浆膜下型疾病(5例)。第四组患者(10例)作为对照,有腹部症状且外周血嗜酸性粒细胞增多原因不明,但未证实有肠道嗜酸性粒细胞浸润。结果发现,40例嗜酸性粒细胞性胃肠炎患者中有20例有过敏史。40例中有9例外周血嗜酸性粒细胞未增多。浆膜下型疾病患者在表现(腹胀、腹水)、嗜酸性粒细胞计数较高以及对类固醇治疗的显著反应方面与其他组不同。在人口统计学因素、出现的症状(腹痛、恶心、体重减轻、腹泻)和实验室参数方面,其他患者相似。40例患者中有10例血沉中度升高。该疾病可累及胃肠道的任何部位;1例患者食管有嗜酸性粒细胞浸润记录,2例患者结肠有嗜酸性粒细胞浸润记录。40例中有5例经内镜活检漏诊,可能是因为病变呈斑片状。即使在没有外周血嗜酸性粒细胞增多的情况下,对于不明原因的胃肠道症状进行鉴别诊断时也应考虑嗜酸性粒细胞性胃肠炎。