Htoo Arkar, George Rose S, Mian Badar M, Akgul Mahmut
Department of Pathology and Laboratory Medicine, Albany Medical Center, Albany, NY, USA.
Department of Surgery in the Division of Urology at Albany Medical College, Albany, NY, USA.
Acad Pathol. 2023 Apr 11;10(2):100078. doi: 10.1016/j.acpath.2023.100078. eCollection 2023 Apr-Jun.
Eosinophilic cystitis (EC) is an uncommon diagnosis, mimicking urothelial carcinoma. Multiple etiologies including iatrogenic, infectious, and neoplastic have been suggested, effecting both adults and pediatric population. A retrospective clinicopathologic review of patients with EC in our institution between 2003 and 2021 was conducted. Age, gender, presenting symptoms, cystoscopic findings, and history of urinary bladder instrumentation were recorded. Histologically, urothelial and stromal changes were noted, and mucosal eosinophilic infiltration was graded as mild (scattered eosinophils in the lamina propria), moderate (visible small clusters of eosinophils without brisk reactive changes), or severe (dense eosinophilic infiltrate with ulcer formation and/or muscularis propria infiltration). Twenty-seven patients (male to female ratio = 18/9, median age 58 [12-85 years]), of whom two were in the pediatric age group were identified. Leading presenting symptoms were hematuria (9/27, 33%), neurogenic bladder (8/27, 30%), and lower urinary tract symptoms (5/27, 18%). Four of 27 (15%) patients had history of urothelial carcinoma of urinary bladder. Cystoscopy commonly revealed erythematous mucosa (21/27, 78%) and/or urinary bladder mass (6/27, 22%). Seventeen of 27 (63%) of patients had history of long-term/frequent catheterization. Mild, moderate, and severe eosinophilic infiltrates were seen in 4/27 (15%), 9/27 (33%), and 14/27 (52%) of cases. Proliferative cystitis (19/27, 70%) and granulation tissue (15/27, 56%) were additional common findings. All cases of long-term/frequent instrumentation cases had moderate or severe eosinophilic infiltrate. EC should be in the differential diagnosis; particularly in patients with long term/frequent catheterization.
嗜酸性膀胱炎(EC)是一种罕见的诊断,易与尿路上皮癌混淆。已提出多种病因,包括医源性、感染性和肿瘤性,影响成人和儿童人群。对2003年至2021年间我院EC患者进行回顾性临床病理分析。记录年龄、性别、症状、膀胱镜检查结果及膀胱器械操作史。组织学上,观察到尿路上皮和间质变化,黏膜嗜酸性粒细胞浸润分为轻度(固有层散在嗜酸性粒细胞)、中度(可见小簇嗜酸性粒细胞,无明显反应性改变)或重度(密集嗜酸性粒细胞浸润伴溃疡形成和/或肌层浸润)。共确定27例患者(男:女 = 18/9,中位年龄58岁[12 - 85岁]),其中2例为儿童。主要症状为血尿(9/27,33%)、神经源性膀胱(8/27,30%)和下尿路症状(5/27,18%)。27例患者中有4例(15%)有膀胱尿路上皮癌病史。膀胱镜检查常见黏膜红斑(21/27,78%)和/或膀胱肿物(6/27,22%)。27例患者中有17例(63%)有长期/频繁导尿史。轻度、中度和重度嗜酸性粒细胞浸润分别见于4/27(15%)、9/27(33%)和14/27(52%)的病例。增生性膀胱炎(19/27,70%)和肉芽组织(15/27,56%)是另外常见的表现。所有长期/频繁器械操作病例均有中度或重度嗜酸性粒细胞浸润。EC应列入鉴别诊断;尤其是长期/频繁导尿的患者。