Mainali Naba Raj, Jalota Leena, Pathak Ranjan, Jain Shashank
Department of Medicine, Reading Health System, West Reading, Pennsylvania, USA.
BMJ Case Rep. 2014 Jul 3;2014:bcr2013202563. doi: 10.1136/bcr-2013-202563.
Retroperitoneal extramedullary plasmacytoma (EMP) is a rare condition that often poses a diagnostic challenge. This is mainly due to its unusual location and non-specific symptoms especially in its early stages. Retroperitoneal plasmacytoma with renal involvement is an extremely rare entity and to date, less than 25 cases have been reported in the literature. We describe a case of a 65-year-old woman with primary retroperitoneal plasmacytoma, confirmed by ultrasound-guided biopsy and histopathological examination, with unilateral left obstructive hydronephrosis and metastasis to the lungs. Our patient was started on chemotherapy to which she did not respond. Subsequently, she resorted to palliative measures. Our case highlights key aspects of clinical presentation, diagnosis and treatment options available for management of retroperitoneal plasmacytoma.
腹膜后髓外浆细胞瘤(EMP)是一种罕见疾病,常带来诊断挑战。这主要归因于其不寻常的位置和非特异性症状,尤其是在疾病早期。累及肾脏的腹膜后浆细胞瘤极为罕见,迄今为止,文献报道不足25例。我们描述了一例65岁女性原发性腹膜后浆细胞瘤病例,经超声引导下活检和组织病理学检查确诊,伴有左侧单侧梗阻性肾积水和肺转移。我们的患者开始接受化疗,但无反应。随后,她采取了姑息治疗措施。我们的病例突出了腹膜后浆细胞瘤临床表现、诊断及可用治疗方案的关键要点。