Department of Surgical Pathology, Hospital Clínico, San Carlos, Madrid, Spain.
Department of Gastroenterology, Hospital Clínico, San Carlos, Madrid, Spain.
Pathol Res Pract. 2018 Jan;214(1):100-104. doi: 10.1016/j.prp.2017.09.029. Epub 2017 Oct 18.
INTRODUCTION: Primary eosinophilic colitis (EC) in adults is a rare and poorly studied disease, with 3 case series, 2 database-based studies and 52 case reports published to date. METHODS: Retrospective study of all adult EC cases diagnosed in a large tertiary hospital (Hospital Clínico San Carlos, Madrid) between 2006 and 2016. We included all cases with a histopathological diagnosis of EC and we selected only those cases that were clinically recognized primary EC. We report their clinical, endoscopic and histopathological features and review the literature on this topic. RESULTS: We identified 22 primary EC cases. Patients were mostly women (77%) with a mean age of 41 years. 4 patients (18%) had coexistent allergic diseases. Most patients consulted with diarrhea (86%) and 3 patients also suffered from rectal bleeding. Blood tests showed peripheral eosinophilia in 4 cases (18%). 19 patients had no endoscopic lesions, 2 had features of unspecific colitis and one showed features suggestive of IBD. Mean and maximum number of eosinophils per high power field ranged from 16 to 199 and 20 to 253 (mean: 48 and 70). They were mainly located in the lamina propria and most cases were associated with signs of eosinophil activation. Most patients were treated by corticosteroids, diet or budesonide and the result of treatment was generally good. No complications or recurrences were reported. CONCLUSIONS: EC etiology and pathogenesis is unknown. Its clinical, endoscopical and imaging features are not specific, and clear histopathological criteria are lacking. Identification of signs of eosinophilic activation could be helpful.
简介:成人原发性嗜酸性粒细胞性结肠炎(EC)是一种罕见且研究甚少的疾病,目前已有 3 个病例系列研究、2 项基于数据库的研究和 52 个病例报告。
方法:回顾性分析 2006 年至 2016 年期间在一家大型三级医院(马德里圣卡洛斯临床医院)诊断的所有成人 EC 病例。我们纳入了所有经组织病理学诊断为 EC 的病例,并仅选择了那些临床上被认为是原发性 EC 的病例。我们报告了其临床、内镜和组织病理学特征,并复习了该主题的文献。
结果:我们共确定了 22 例原发性 EC 病例。患者大多为女性(77%),平均年龄为 41 岁。4 例(18%)患者合并过敏性疾病。大多数患者以腹泻(86%)就诊,3 例患者还伴有直肠出血。4 例(18%)患者的外周血嗜酸性粒细胞增多。19 例患者无内镜下病变,2 例患者存在非特异性结肠炎特征,1 例患者存在提示 IBD 的特征。高倍镜视野下嗜酸性粒细胞的平均和最大数目分别为 16-199 个和 20-253 个(平均:48 和 70)。它们主要位于固有层,大多数病例与嗜酸性粒细胞活化的迹象相关。大多数患者接受了皮质类固醇、饮食或布地奈德治疗,治疗效果通常较好。未报告并发症或复发。
结论:EC 的病因和发病机制尚不清楚。其临床、内镜和影像学特征不具有特异性,且缺乏明确的组织病理学标准。识别嗜酸性粒细胞活化的迹象可能有帮助。
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