Bladder extramedullary plasmacytoma and synchronous bladder urothelial transitional cell carcinoma: A case report and review of the literature.

Open Access Journal of Urology Pub Date : 2011-02-15 eCollection Date: 2011-01-01 DOI:10.2147/OAJU.S10897
Karan Wadhwa, Raj Singh, Lemke Z Solomon
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引用次数: 4

Abstract

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.

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膀胱髓外浆细胞瘤及同步膀胱尿路上皮移行细胞癌1例报告及文献复习。
一名69岁男性,表现为突然出现肉眼可见的血尿。膀胱超声检查显示膀胱后部肿块,随后的柔性膀胱镜检查仅显示不规则尿路上皮区域。初始全麻细胞镜和活检显示常规G2/3 T1 TCC。进一步正式切除该不规则区域的组织学显示原位癌和非典型细胞群,细胞核增大,核仁突出,细胞质数量变化,显示浆细胞特征。免疫组化符合浆细胞瘤。当超声显示软性膀胱镜检查未发现的肿块时,必须高度怀疑,建议活检/切除以排除髓外浆细胞瘤(EMP)作为病因。膀胱EMP是一种罕见的疾病,文献中仅报道了21例。在本报告中,我们描述了另一例膀胱EMP合并尿路上皮同步移行细胞癌(TCC)。我们还强调了重要的组织病理学发现,并回顾了目前的文献,报告了现有方法治疗这种罕见形式的膀胱癌的结果。我们认为这是首例同时出现膀胱EMP和尿路上皮性TCC的病例。emp是高度放射敏感的肿瘤,在头颈部疾病的情况下,根治性放疗后10年生存率约为65%。由于原发性膀胱EMP病例报道较少,最佳治疗方案仍不清楚。与其他解剖部位保持一致,目前的治疗是基于假设的根治性放疗的益处,并且在没有全身性疾病证据的患者中预后似乎更好。
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