Concomitant Lupus Enteritis and Lupus Cystitis: Case Report and Literature Review.

IF 0.8
Doan Nguyen, Huong Nguyen, Uyen Tran, Luu Le
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Abstract

Lupus enteritis and lupus cystitis share a common etiology, characterized by smooth muscle dysmotility resulting from immune complex-mediated damage. This paper describes a case of a patient presenting with concomitant lupus enteritis and lupus cystitis without a prior systemic lupus erythematosus (SLE) diagnosis. The onset of symptoms occurred five months earlier with frequent loose stools, persistent abdominal pain, nausea, vomiting, and a significant weight loss of 16 kg. The patient presented with abdominal pain, distension, dysuria, and urinary urgency lasting for a week. A computed tomography scan upon admission revealed diffuse thickening of the gastric, intestinal, and colon walls, as well as cystitis, ureteral dilation, and bilateral hydronephrosis. Extensive screening excluded infections and other autoimmune diseases, confirming SLE according to the 2019 EULAR/ACR criteria, with a high SLE disease activity index score of 18 points. Treatment with corticosteroids resulted in symptomatic improvement in the intestinal and bladder symptoms and other organ involvements. This case highlights the significance of recognizing autoimmune causes, such as lupus, in cases of widespread gastrointestinal and bladder inflammation.

狼疮肠炎及狼疮膀胱炎合并病例报告及文献复习。
狼疮肠炎和狼疮膀胱炎有一个共同的病因,其特征是由免疫复合物介导的损伤引起的平滑肌运动障碍。这篇论文描述了一个病例的病人提出伴随狼疮肠炎和狼疮膀胱炎没有先前的系统性红斑狼疮(SLE)诊断。症状出现早5个月,出现频繁稀便、持续性腹痛、恶心、呕吐,体重明显减轻16公斤。患者腹痛、腹胀、排尿困难、尿急持续一周。入院时的计算机断层扫描显示胃、肠和结肠壁弥漫性增厚,以及膀胱炎、输尿管扩张和双侧肾积水。广泛筛查排除了感染和其他自身免疫性疾病,根据2019年EULAR/ACR标准确认SLE, SLE疾病活动性指数高,得分为18分。皮质类固醇治疗导致肠道和膀胱症状及其他器官受累的症状改善。本病例强调了在广泛的胃肠道和膀胱炎症病例中识别自身免疫性原因(如狼疮)的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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