Modi Rangesh, Erazo Gloria, Anand Reddy
Department of Internal Medicine, Section of Gastroenterology, Hepatology and Nutrition, University of Chicago Medicine, Chicago, IL.
Department of Internal Medicine, Texas Tech University Health Sciences Center Permian Basin, Odessa, TX.
ACG Case Rep J. 2024 Aug 29;11(9):e01478. doi: 10.14309/crj.0000000000001478. eCollection 2024 Sep.
We report the case of a 70-year-old woman diagnosed with neural epidermal growth factor-like 1 antigen-positive membranous nephropathy and nephrotic syndrome. Following thorough exclusion of autoimmune diseases, medications, or infections as potential causes, colonoscopy was performed as part of malignancy evaluation, revealing an 18 mm villous adenoma in the sigmoid colon and a 7 mm tubulovillous adenoma in the cecum. Despite the absence of gastrointestinal symptoms initially and the absence of high-grade dysplasia in the pathology report, the patient experienced a remarkable improvement in symptoms and a reduction in nephrotic-range proteinuria following polypectomy, observed within a few months.
我们报告了一例70岁女性患者,诊断为神经表皮生长因子样1抗原阳性的膜性肾病和肾病综合征。在彻底排除自身免疫性疾病、药物或感染等潜在病因后,作为恶性肿瘤评估的一部分进行了结肠镜检查,结果显示乙状结肠有一个18毫米的绒毛状腺瘤,盲肠有一个7毫米的管状绒毛状腺瘤。尽管患者最初没有胃肠道症状,且病理报告中没有高级别发育异常,但在息肉切除术后几个月内,患者症状显著改善,肾病范围蛋白尿减少。