Kufukihara Ryohei, Niwa Naoya, Mizuno Ryuichi, Ohara Kentaro, Mikami Shuji, Kikuchi Eiji, Oya Mototsugu
Department of Urology, Keio University School of Medicine, Tokyo, Japan.
Department of Urology, Keio University School of Medicine, Tokyo, Japan,
Urol Int. 2019;103(4):488-490. doi: 10.1159/000495570. Epub 2018 Dec 13.
Immunoglobulin G4-related disease (IgG4-RD) is a recently described inflammatory disease with multiorgan involvement. Although there were reports of IgG4-related kidney disease or prostatitis, this disease rarely presents in the bladder. In this report, we describe a case of IgG4-RD arising from bladder wall. This patient had a past history of autoimmune pancreatitis and presented with incidental bladder tumor. Magnetic resonance imaging showed low signal intensity tumor on T2-weighted image, and no invasion to the muscular layer. We performed transurethral resection. Pathological findings showed that there were chronic inflammatory changes infiltrates under the epithelium, and IgG4-positive plasma cells were scattered throughout the lesion. They met the pathological diagnostic criteria for IgG4-RD. We think this is the first case of IgG4-RD arising from and confined to the inside of the bladder wall.
免疫球蛋白G4相关性疾病(IgG4-RD)是一种最近被描述的累及多器官的炎症性疾病。尽管有关于IgG4相关性肾病或前列腺炎的报道,但该疾病很少累及膀胱。在本报告中,我们描述了一例起源于膀胱壁的IgG4-RD病例。该患者有自身免疫性胰腺炎病史,因偶然发现膀胱肿瘤就诊。磁共振成像显示T2加权像上肿瘤呈低信号强度,未侵犯肌层。我们进行了经尿道切除术。病理结果显示上皮下有慢性炎症浸润,IgG4阳性浆细胞散在分布于整个病变中。它们符合IgG4-RD的病理诊断标准。我们认为这是首例起源于并局限于膀胱壁内的IgG4-RD病例。