Mohsin Muhammad Bilal, Rasool Uswah, Rana Laiba A, Hashmi Tahir M
Internal Medicine, Shifa International Hospital Islamabad, Islamabad, PAK.
Rheumatology, Shifa International Hospital Islamabad, Islamabad, PAK.
Cureus. 2024 Sep 9;16(9):e68997. doi: 10.7759/cureus.68997. eCollection 2024 Sep.
We discuss the case of a 45-year-old male with complaints of abdominal pain, loose stools with on and off melena, and multiple joint pains bilaterally. The patient reported having similar episodes in the past, with slight variations in the symptoms and relief with short courses of steroids. Initially, a workup was done to identify an infectious etiology of the diarrhea. However, no such cause was identified. Similarly, an autoimmune profile was ordered to investigate the patient's joint complaints, albeit with no conclusive findings. His renal function tests and urinalysis showed findings indicative of an acute kidney injury. This prompted an antineutrophil cytoplasmic antibody (ANCA) profile, which was positive for c-ANCA. A diagnosis of granulomatosis with polyangiitis (GPA) was made, and the patient was started on pulse steroid and immunomodulator therapy with improvement in the patient's condition. This case is atypical due to its involvement of the gastrointestinal system, which is relatively rare, as well as polyarthritis of the small joints.
我们讨论了一名45岁男性患者的病例,该患者主诉腹痛、伴有间歇性黑便的稀便以及双侧多关节疼痛。患者报告过去有类似发作,症状略有不同,短期使用类固醇后症状缓解。最初,进行了一系列检查以确定腹泻的感染性病因。然而,未发现此类病因。同样,为调查患者的关节问题进行了自身免疫相关检查,但没有确凿结果。他的肾功能检查和尿液分析结果显示有急性肾损伤的迹象。这促使进行抗中性粒细胞胞浆抗体(ANCA)检测,结果显示c-ANCA呈阳性。最终诊断为肉芽肿性多血管炎(GPA),患者开始接受脉冲类固醇和免疫调节剂治疗,病情有所改善。该病例具有非典型性,因为它累及了相对罕见的胃肠道系统以及小关节多关节炎。