Wadhwa Karan, Singh Raj, Solomon Lemke Z
Department of Urology, Queen Alexandra Hospital, Portsmouth, UK.
Open Access J Urol. 2011 Feb 15;3:25-7. doi: 10.2147/OAJU.S10897. eCollection 2011.
A 69-year-old man presented with sudden onset of macroscopic hematuria. While an ultrasound of the bladder revealed a posterior bladder mass, subsequent flexible cystoscopy demonstrated only an area of irregular urothelium. Initial general anesthetic cytoscopy and biopsy revealed conventional G2/3 T1 TCC. Histology of a further formal resection of this irregular area revealed carcinoma-in-situ and population of atypical cells with enlarged nuclei, prominent nucleoli, and varying quantities of cytoplasm showing plasma cell features. The immunohistochemistry was consistent with a plasmacytoma. There must be a high index of suspicion when ultrasound demonstrates a mass not detected by flexible cystoscopy, and biopsies/resection are advised to exclude extramedullary plasmacytoma (EMP) as the cause. EMP of the urinary bladder is a rare entity with only 21 cases reported in the literature. In this report we describe a further case of EMP of the bladder associated with synchronous transitional cell carcinoma (TCC) of the urothelium. We also highlight the important histopathological findings and review the current literature to report the outcomes of existing approaches to management of this rare form of bladder cancer. We believe this to be the first case reported in which a patient presented concurrently with bladder EMP and urothelial TCC. EMPs are highly radiosensitive tumors and in the case of head/neck disease, survival at 10 years is in the order of 65% following radical radiotherapy. Given the paucity of reported cases of primary bladder EMP, the optimal treatment regime remains unclear. In keeping with other anatomical sites current treatment is based to the assumed benefit of radical radiotherapy and prognosis appears to be better in those with no evidence of systemic disease.
一名69岁男性突发肉眼血尿。膀胱超声检查发现膀胱后部有一肿块,随后的软性膀胱镜检查仅发现一处不规则尿路上皮区域。初次全身麻醉下的膀胱镜检查及活检显示为常规的G2/3 T1期移行细胞癌。对该不规则区域进一步进行正式切除后的组织学检查发现原位癌以及一群非典型细胞,这些细胞细胞核增大、核仁突出,且有不同数量的细胞质,具有浆细胞特征。免疫组化结果与浆细胞瘤一致。当超声显示出软性膀胱镜未检测到的肿块时,必须高度怀疑,建议进行活检/切除以排除髓外浆细胞瘤(EMP)作为病因。膀胱EMP是一种罕见疾病,文献中仅报道过21例。在本报告中,我们描述了另一例与尿路上皮同步移行细胞癌(TCC)相关的膀胱EMP病例。我们还强调了重要的组织病理学发现,并回顾了当前文献,以报告现有治疗这种罕见膀胱癌方法的结果。我们认为这是首例报道的患者同时患有膀胱EMP和尿路上皮TCC的病例。EMP是对放疗高度敏感的肿瘤,对于头颈部疾病,根治性放疗后10年生存率约为65%。鉴于原发性膀胱EMP的报道病例较少,最佳治疗方案仍不明确。与其他解剖部位一致,目前的治疗基于根治性放疗的假定益处,且对于无全身疾病证据的患者,预后似乎更好。