Xu Hewei, Chen Zhengsen, Shen Baixin, Wei Zhongqing
Urology Department, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Medicine (Baltimore). 2020 Jul 10;99(28):e20825. doi: 10.1097/MD.0000000000020825.
Primary bladder mucosa-associated lymphoid tissue (MALT) lymphoma is a rare tumor. To date, the PubMed database contains only 39 English articles covering 63 cases of primary bladder MALT lymphoma. Herein, we report a case of this disease and review the current literature.
A 77-year-old woman presented with frequent urination, urinary urgency, and dysuria for 3 years. In the past 3 years, the patient's symptoms recurred and progressively worsened, and she was admitted to the hospital.
A histopathological examination revealed the bladder mass as a tumor with high proliferation of atypical B-lymphocytes. Immunohistochemistry showed positive results for CD20, PAX-5, Ki-67, BCL-2, and CD21 and negative results for CD10, MUM1, TDT, and cyclin D1. These data supported the diagnosis of primary bladder MALT lymphoma.
A transurethral resection of bladder tumor was performed to treat the disease.
The patient was alive and healthy at the 15-month follow-up.
Primary bladder MALT lymphoma is a rare disease and can be easily missed or misdiagnosed before achieving a histological confirmation. Surgery may be the best choice for both diagnosis and treatment.
原发性膀胱黏膜相关淋巴组织(MALT)淋巴瘤是一种罕见肿瘤。截至目前,PubMed数据库中仅有39篇英文文章报道了63例原发性膀胱MALT淋巴瘤。在此,我们报告1例该疾病病例并回顾当前文献。
一名77岁女性,出现尿频、尿急及尿痛3年。在过去3年中,患者症状反复且逐渐加重,遂入院治疗。
组织病理学检查显示膀胱肿物为非典型B淋巴细胞高度增殖的肿瘤。免疫组化显示CD20、PAX-5、Ki-67、BCL-2和CD21呈阳性,CD10、MUM1、TDT和细胞周期蛋白D1呈阴性。这些数据支持原发性膀胱MALT淋巴瘤的诊断。
行经尿道膀胱肿瘤切除术治疗该疾病。
在15个月的随访中,患者存活且健康。
原发性膀胱MALT淋巴瘤是一种罕见疾病,在获得组织学确诊之前很容易被漏诊或误诊。手术可能是诊断和治疗的最佳选择。