Khan Bushra Ali, Saleem Nida, Hassan Danyal, Kiani Shabaz, Haneef Muhammad
Shifa International Hospital, H-8/4, Pitras Bukhari Road, Islamabad, Pakistan.
Case Rep Nephrol. 2022 Feb 4;2022:1079300. doi: 10.1155/2022/1079300. eCollection 2022.
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.
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,很少同时存在。我们报告一例21岁男性的病史,该患者最初表现为血性腹泻,随后经结肠活检诊断为溃疡性结肠炎。存在临床无症状的肾功能损害,导致终末期肾病,需要进行血液透析,这可能继发于狼疮性肾炎,因为检测到狼疮特异性抗体呈阳性。除此之外,根据脑部CT检查结果诊断为狼疮合并早期交通性脑积水,免疫抑制治疗开始后临床反应良好。对于有胃肠道(GI)表现的SLE患者,必须牢记溃疡性结肠炎的可能性。交通性脑积水是SLE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治疗反应良好。因此,即使是终末期肾病(ESRD)患者,也必须尝试使用免疫抑制药物来控制肾脏外罕见的狼疮表现。