Gheorghe C, Aposteanu G, Popescu C, Gheorghe L, Oproiu A, Popescu I
Department of Gastroenterology, Fundeni Hospital, Carol Davila University of Medicine, Bucharest, Romania.
Hepatogastroenterology. 1998 May-Jun;45(21):738-41.
Crohn's disease of the esophagus is rare, and it is very unusual for it to be located only in the esophagus. We report a case of Crohn's disease confined to the esophagus in a 26-year-old female. The patient was admitted because of progressive dysphagia, odynophagia and weight loss. A barium-swallow examination showed an irregular narrowing of the esophagus below the level of the aortic arch which was 15 cm long, with marginal ulcers and a pseudopolypoid appearance of the mucosa; a computed tomographic scan of the thorax revealed a thickened esophageal wall. Esophagoscopy revealed an esophageal stricture 25 cm distal to the incisor teeth, 2 mm in diameter, with "punched out" ulcers and pseudopolypoid mucosa. Endobiopsy specimens showed chronic lymphocytic infiltration into the corion in the absence of neutrophils, basal-cell hyperplasia and elongation of the stromal papillae. The patient underwent an esophagectomy through a combined cervico-abdominal approach followed by a cervical esogastrostomy. The specimen was 18 cm long, the thickness of the wall was 1.7 cm with fibrosis involving all layers of the esophageal wall and a cobblestone appearance of the mucosa. A heavy lymphoplasmocytic infiltrate extended from the mucosa deep into the muscularis, fibrosis and granulomas were found transmurally. Crohn's disease of the esophagus is a rare and specific entity which can present in various ways; strictures resembling those from reflux esophagitis or a tumor are common. Diagnosis may be suggested by the presence of a chronic lymphocytic infiltrate with or without non-caseating granulomas, and no histologic evidence of chronic reflux esophagitis.
食管克罗恩病较为罕见,仅局限于食管的情况非常少见。我们报告一例26岁女性的食管克罗恩病病例。该患者因进行性吞咽困难、吞咽痛和体重减轻入院。吞钡检查显示主动脉弓水平以下食管出现不规则狭窄,长度为15厘米,伴有边缘溃疡和黏膜假息肉样外观;胸部计算机断层扫描显示食管壁增厚。食管镜检查发现距门齿25厘米处有食管狭窄,直径2毫米,伴有“凿孔样”溃疡和假息肉样黏膜。内镜活检标本显示在无中性粒细胞的情况下,真皮有慢性淋巴细胞浸润、基底细胞增生和间质乳头延长。患者通过颈腹联合入路接受了食管切除术,随后进行了颈部食管胃吻合术。标本长18厘米,壁厚1.7厘米,食管壁各层均有纤维化,黏膜呈鹅卵石样外观。重度淋巴浆细胞浸润从黏膜延伸至肌层,全层可见纤维化和肉芽肿。食管克罗恩病是一种罕见的特殊疾病,可表现为多种形式;类似反流性食管炎或肿瘤所致的狭窄较为常见。慢性淋巴细胞浸润伴或不伴有非干酪样肉芽肿,且无慢性反流性食管炎的组织学证据时,可提示诊断。