...
首页> 外文期刊>BMC Gastroenterology >The concurrent association of inflammatory polymyositis and Crohn’s ileo-colitis in a Sri Lankan man: a case report of a rare association and literature review
【24h】

The concurrent association of inflammatory polymyositis and Crohn’s ileo-colitis in a Sri Lankan man: a case report of a rare association and literature review

机译:一名斯里兰卡男子同时患有炎症性多发性肌炎和克罗恩回肠结肠炎:一例罕见病例的报道和文献综述

获取原文
           

摘要

Background Crohn’s disease is a relapsing, systemic inflammatory disease affecting the gastrointestinal tract with associated extraintestinal manifestations and immune disorders. Among the few cases reported, the association of Crohn’s disease with polymyositis varies in its complexity and severity. We report here the first known case of inflammatory polymyositis leading to rhabdomyolysis in a male patient diagnosed with Crohn’s ileocolitis. Case presentation A 42-year-old previously healthy man presented with acute polymyositis leading to rhabdomyolysis. The acute nature of the illness raised the suspicion of an infective, toxic, or metabolic insult, which was excluded during further investigations. Prolonged low-grade fever and raised inflammatory markers led to the suspicion of inflammatory polymyositis, which was confirmed by electromyography and muscle histology. In the absence of an infective cause, the concurrent association of prolonged diarrhea containing blood and mucous after recovery from an acute phase of myositis proved a diagnostic challenge. Ileocolonoscopy findings of extensive aphthous ulceration with skip lesions extending to the terminal ileum, and histology showing polymorph infiltration of the lamina propria, transmural involvement, and micro abscess formation was suggestive of Crohn’s disease. Sensory motor axonal peripheral neuropathy, which is another rare association of inflammatory bowel disease, was also present. Conclusion An unrecognized genetic predisposition or altered gut permeability causing disruption of the gut immune barrier triggering an immune response against skeletal muscles may have contributed to this unique association. Both polymyositis and Crohn’s ileocolitis responded well to corticosteroids and azathioprine, which is supportive of their immune pathogenesis. Myositis can be considered to be a rare extraintestinal manifestation of Crohn’s disease and can be used in the differential diagnosis of corticosteroid or hypokalemia-induced myopathy in Crohn’s disease.
机译:背景克罗恩氏病是一种复发性全身性炎症性疾病,会影响胃肠道并伴有相关的肠外表现和免疫紊乱。在少数报道的病例中,克罗恩氏病与多发性肌炎的关系在复杂性和严重性方面有所不同。我们在这里报告了首例已知的炎症性多发性肌炎,该病例在被诊断为克罗恩氏回肠结肠炎的男性患者中导致横纹肌溶解。病例介绍一名42岁以前健康的人,出现了导致横纹肌溶解的急性多发性肌炎。这种疾病的急性性质引起了人们对传染性,中毒或新陈代谢的侮辱的怀疑,在进一步的调查中将其排除在外。长时间的低烧和炎性标志物升高引起对炎性多肌炎的怀疑,这已通过肌电图和肌肉组织学证实。在没有感染原因的情况下,从肌炎急性期恢复后,含有血液和粘液的长时间腹泻并存,证明了诊断上的挑战。结肠镜检查发现广泛的口腔溃疡,跳跃性病变延伸至回肠末端,组织学显示固有层多态性浸润,透壁受累和微脓肿形成提示克罗恩病。还存在感觉运动轴突周围神经病,这是炎症性肠病的另一种罕见关联。结论无法识别的遗传易感性或改变的肠道通透性导致肠道免疫屏障的破坏,从而触发了针对骨骼肌的免疫反应,可能与这种独特的联系有关。多发性肌炎和克罗恩氏回肠结肠炎对皮质类固醇和硫唑嘌呤的反应都很好,这支持了它们的免疫发病机理。肌炎被认为是克罗恩病罕见的肠道外表现,可用于克罗恩病中皮质类固醇激素或低钾血症引起的肌病的鉴别诊断。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号