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原发性尿道浆细胞瘤:一例报告及文献复习

Primary urethral plasmacytoma: a case report and literature review.

作者信息

Gokce Ozgur, Acar Omer, Tunc Murat, Kilicaslan Isin, Esen Tarik, Ozcan Faruk

机构信息

Department of Urology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.

出版信息

Kaohsiung J Med Sci. 2008 May;24(5):274-7. doi: 10.1016/S1607-551X(08)70153-0.

Abstract

Plasmacytomas of the urethra are extremely rare neoplasias; they may occur as isolated tumors or concomitantly with generalized multiple myeloma. Herein, we describe the clinical presentation and characteristics of a patient with primary plasmacytoma of the urethra. A 51-year-old man presented with terminal hematuria and a palpable penile mass. Magnetic resonance urethrography revealed a 3-cm long stenotic segment along which the urethral mucosa was found to be irregular. On urethroscopy, papillary mucosal projections extending to the presphincteric area were noted. Lesions were found to be composed primarily of neoplastic plasma cells capable of producing mainly lambda light chain. Upon diagnosis, the patient received external beam radiation therapy targeting the pelvic region. The lesion diminished in size progressively during the treatment course. He was disease-free after 6 months. Although it is a relatively rare disease, primary urethral plasmacystoma should be considered in the differential diagnosis of urethral tumors and radiation therapy should be an integral part of the treatment strategy.

摘要

尿道浆细胞瘤是极为罕见的肿瘤;它们可能以孤立性肿瘤的形式出现,或与全身性多发性骨髓瘤同时发生。在此,我们描述一名原发性尿道浆细胞瘤患者的临床表现和特征。一名51岁男性出现终末血尿和可触及的阴茎肿块。磁共振尿道造影显示一段3厘米长的狭窄段,沿该段尿道黏膜不规则。尿道镜检查时,注意到乳头状黏膜突起延伸至括约肌前区。病变主要由能够产生主要为λ轻链的肿瘤性浆细胞组成。诊断后,患者接受了针对盆腔区域的外照射放疗。在治疗过程中,病变大小逐渐缩小。6个月后他无病生存。尽管这是一种相对罕见的疾病,但在尿道肿瘤的鉴别诊断中应考虑原发性尿道浆细胞瘤,放疗应是治疗策略的一个组成部分。

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