Tu Xi, Zhuang Xiyao, Li Fen, Huang Chaoyou, Qian Youliang
Department of Urology, Chengdu Second People's Hospital, Chengdu, Sichuan, China.
Department of Internal Medicine, Chengdu Shuangliu Hospital of Traditional Chinese Medicine, Chengdu, Sichuan, China.
Front Oncol. 2023 Jan 5;12:1042459. doi: 10.3389/fonc.2022.1042459. eCollection 2022.
Primary bladder mucosa-associated lymphoid tissue (MALT) lymphoma is an extremely rare bladder tumor. Only scarce reports have been reported. We hereby report a case of an 81-year-old female patient with bladder tumor presenting with frequent urination and dysuria, whose pelvic magnetic resonance imaging (MRI) considered bladder cancer. She underwent transurethral resection of the bladder tumor (TURBT), and histopathology confirmed the mass to be bladder MALT lymphoma. The patient refused further treatment, and no disease recurrence one year after surgery. The current data are insufficient to draw conclusions about the long-term efficacy of treatment for this tumor, regular follow-up is necessary. To further understand the clinical features, pathology, treatment and prognosis of this tumor, we have searched the literature from 1990 to the present, analyzing a total of 64 cases of primary MALT lymphoma.
原发性膀胱黏膜相关淋巴组织(MALT)淋巴瘤是一种极其罕见的膀胱肿瘤。仅有少量相关报道。我们在此报告一例81岁女性膀胱肿瘤患者,该患者表现为尿频和排尿困难,其盆腔磁共振成像(MRI)考虑为膀胱癌。她接受了经尿道膀胱肿瘤切除术(TURBT),组织病理学证实肿块为膀胱MALT淋巴瘤。患者拒绝进一步治疗,术后一年无疾病复发。目前的数据不足以得出关于该肿瘤治疗长期疗效的结论,有必要进行定期随访。为进一步了解该肿瘤的临床特征、病理、治疗及预后,我们检索了1990年至今的文献,共分析了64例原发性MALT淋巴瘤病例。