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慢性非特异性溃疡性十二指肠空肠回肠炎:4例报告

Chronic non-specific ulcerative duodenojejunoileitis: report of four cases.

作者信息

Modigliani R, Poitras P, Galian A, Messing B, Guyet-Rousset P, Libeskind M, Piel-Desruisseaux J L, Rambaud J C

出版信息

Gut. 1979 Apr;20(4):318-28. doi: 10.1136/gut.20.4.318.

Abstract

Four patients with chronic non-specific ulcerative duodenojejunoileitis (CNSUDJI) are reported. The clinical picture included abdominal pain, fever, and a malabsorption syndrome. Main rediological findings were diffuse narrowing of the jejunal loops with total effacement of the mucosal folds. Multiple peroral biopsies of the small intestine showed various degrees of mucosal abnormalities from total villous atrophy to normal villi, but ulcerations were diagnosed only by operative full thickness biopsies or resection of the small bowel. The ulcerative process was associated with well-documented coeliac disease in two patients: in one of them it occurred as a fatal complication involving also the colon, three years after the start of a gluten free diet, while the disease was in full clinical and histological remission. In the other case, coeliac disease was revealed by obstructive symptoms due to stenosing ulcerations; five months after surgical resection of the stenosis, institution of a gluten free diet induced a dramatic improvement. In the two other patients ulcerations were not associated with coeliac disease: one of them had a patchy villous atrophy and resisted a gluten free diet and total parenteral nutrition; she was improved by and dependent upon steroids but finally died. The last patient had normal villous height; ulcerations were located exclusively along the mesenteric border of the small bowel; he had a low-grade protracted evolution resisting any form of therapy and developed a peripheral neuropathy of unknown aetiology. On the basis of our cases and of a review of the literature the discussion focuses on the difficulty in diagnosing CNSUDJI, its relationship with coeliac disease, and its management and prognosis.

摘要

本文报告了4例慢性非特异性溃疡性十二指肠空肠回肠炎(CNSUDJI)患者。临床表现包括腹痛、发热和吸收不良综合征。主要影像学表现为空肠袢弥漫性狭窄,黏膜皱襞完全消失。多次经口小肠活检显示从完全绒毛萎缩到正常绒毛的不同程度黏膜异常,但仅通过手术全层活检或小肠切除才能诊断溃疡。在2例患者中,溃疡性病变与确诊的乳糜泻相关:其中1例在开始无麸质饮食3年后,作为致命并发症出现,累及结肠,而此时疾病处于完全临床和组织学缓解期。在另一例中,由于狭窄性溃疡导致的梗阻症状揭示了乳糜泻;狭窄手术切除5个月后,开始无麸质饮食使病情显著改善。另外2例患者的溃疡与乳糜泻无关:其中1例有斑片状绒毛萎缩,对无麸质饮食和全胃肠外营养无反应;她经类固醇治疗后病情改善但仍依赖类固醇,最终死亡。最后1例患者绒毛高度正常;溃疡仅沿小肠系膜缘分布;他病情进展缓慢,对任何形式的治疗均无反应,并出现了病因不明的周围神经病变。基于我们的病例及文献复习,讨论集中在CNSUDJI的诊断困难、其与乳糜泻的关系以及治疗和预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0186/1412403/e29af1b2880a/gut00449-0073-a.jpg

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