狼疮性肾炎、溃疡性结肠炎和通讯性脑积水共存:一个21岁男性的报告。

Case Reports in Nephrology Pub Date : 2022-02-04 eCollection Date: 2022-01-01 DOI:10.1155/2022/1079300
Bushra Ali Khan, Nida Saleem, Danyal Hassan, Shabaz Kiani, Muhammad Haneef
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摘要

系统性红斑狼疮(SLE)和溃疡性结肠炎(UC)是多系统自身免疫性疾病,很少共存。我们报告一个21岁男性的病例史,表现为出血性腹泻,后来,结肠活检诊断为溃疡性结肠炎。临床无症状的肾脏损害导致终末期肾脏疾病,需要血液透析,可能继发于持续的狼疮肾炎,狼疮特异性抗体检测阳性。除此之外,根据CT脑部表现诊断狼疮合并早期交通性脑积水,临床对免疫抑制治疗的开始反应良好。有胃肠道(GI)表现的SLE患者必须牢记溃疡性结肠炎的可能性很小。沟通性脑积水是SLE中一种罕见的神经学表现,可导致癫痫发作,对类固醇和免疫抑制剂的起始治疗反应良好。因此,即使是患有终末期肾病(ESRD)的患者,也必须进行免疫抑制药物的试验,以遏制肾外罕见的狼疮表现。
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Coexistence of Lupus Nephritis, Ulcerative Colitis, and Communicating Hydrocephalus: A Report of a 21-Year-Old Male.

Systemic lupus erythematosus (SLE) and ulcerative colitis (UC) are multisystem autoimmune disorders that rarely coexist. We report a case history of a 21-year-old male, presenting with bloody diarrhea and, later, diagnosed to have ulcerative colitis on colonic biopsy. There was clinically silent renal impairment leading to end-stage kidney disease requiring hemodialysis possibly secondary to ongoing lupus nephritis as suggested by positive lupus-specific antibodies' detection. Besides this, the diagnosis of lupus associated with early communicating hydrocephalus was made on CT brain findings which clinically responded well to the initiation of immunosuppressive therapy. It is imperative to keep in mind the remote possibility of ulcerative colitis in an SLE patient with gastrointestinal (GI) manifestations. Communicating hydrocephalus is a rare neurological manifestation of SLE leading to seizures and can respond well to the initiation of steroids and immunosuppressants. Therefore, a trial of immunosuppressant medications must be given even in a patient with end-stage renal disease (ESRD) to halter extra renal rare lupus manifestations.

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来源期刊
Case Reports in Nephrology
Case Reports in Nephrology Medicine-Nephrology
CiteScore
1.70
自引率
0.00%
发文量
32
期刊最新文献
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