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显微镜下结肠炎

Microscopic colitis.

作者信息

Stroehlein John R

机构信息

John R. Stroehlein, MD University of Texas MD Anderson Cancer Center, Department of GI Medicine and Nutrition, 1515 Holcombe Boulevard, Houston, TX 77030, USA.

出版信息

Curr Treat Options Gastroenterol. 2007 Jun;10(3):231-6. doi: 10.1007/s11938-007-0016-0.

Abstract

As the diagnosis of microscopic colitis (MC) is made on the basis of histologic criteria, it is crucial to render an accurate microscopic interpretation. Features include 20 or more lymphocytes per 100 epithelial cells, mixed lamina propria inflammatory infiltrate, and preservation of crypt architecture for both lymphocytic and collagenous colitis (CC). CC is further characterized by a collagen band at least 10 mum thick. Although the pathogenesis of MC is poorly understood, medication-induced toxicity to the colonic mucosa is important to recognize, as medication cessation leads to prompt improvement. If MC is mild, symptomatic treatment is all that is needed, because some cases are self-limiting. Budesonide, 9 mg daily for at least 8 weeks, is the best documented treatment of choice for more severe or protracted cases. A 75% response rate has been reported; however, when treatment is discontinued, relapse is common, and longer-term tapering dose therapy often is necessary. There are disadvantages and no advantage to other forms of steroid therapy. Cholestyramine, bismuth, and 5-aminosalicylate derivatives appear to be less efficacious but are reasonable therapeutic options for less severe cases. Use of immunosuppressant therapy such as azathioprine or 6-mercaptopurine should be highly restricted because MC is a benign condition that does not result in other complications. Probiotic therapy with Lactobacillus acidophilus and Bifidobacterium animalis has not been shown to be effective in reducing bowel frequency. Surgical diversion of the fecal stream can control diarrhea and improve histology but is very rarely indicated and should be reserved for highly selected cases of severely symptomatic steroid-refractory MC.

摘要

由于显微镜下结肠炎(MC)的诊断基于组织学标准,因此做出准确的显微镜解释至关重要。其特征包括每100个上皮细胞中有20个或更多淋巴细胞、固有层混合性炎症浸润,以及淋巴细胞性结肠炎和胶原性结肠炎(CC)的隐窝结构保留。CC的进一步特征是有一条至少10微米厚的胶原带。尽管MC的发病机制尚不清楚,但认识到药物对结肠黏膜的毒性很重要,因为停药后病情会迅速改善。如果MC病情较轻,对症治疗即可,因为有些病例是自限性的。布地奈德,每日9毫克,至少服用8周,是更严重或病程较长病例的最佳记录治疗选择。据报道有效率为75%;然而,停药后复发很常见,通常需要长期逐渐减量治疗。其他形式的类固醇疗法有缺点且无优势。消胆胺、铋剂和5-氨基水杨酸衍生物似乎疗效较差,但对于病情较轻的病例是合理的治疗选择。应严格限制使用硫唑嘌呤或6-巯基嘌呤等免疫抑制疗法,因为MC是一种良性疾病,不会导致其他并发症。嗜酸乳杆菌和动物双歧杆菌的益生菌疗法尚未显示能有效减少排便次数。粪便转流手术可以控制腹泻并改善组织学表现,但很少需要进行,应仅用于极少数有严重症状的类固醇难治性MC病例。

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