Khandakar Binny, Maiti Moumita, Dey Soumit, Ray Prasenjit Sen, Bhattacharyya Palas, Sarkar Ranu
Department of Pathology, Nil Ratan Sircar Medical College & Hospital, KOLKATA, INDIA.
Turk Patoloji Derg. 2018;34(3):251-254. doi: 10.5146/tjpath.2015.01340.
Ewing sarcoma/primitive neuroectodermal tumor (PNET) is a high-grade malignant neoplasm commonly affecting bones of the thoracic region. Primary Ewing sarcoma/PNET of the kidney is exceptional; it commonly affects young adults and is rarely reported in children. Here we describe a case of renal PNET in a 10-year-old girl who presented at our institute with haematuria and abdominal lump. Computer tomography scan revealed a huge mass in the right kidney. Computer tomography-guided aspiration from the mass showed cytomorphological features of a small blue round cell tumor. The patient underwent right radical nephrectomy. Histopathology with supplementary immunohistochemistry confirmed the diagnosis of PNET. She has been receiving treatment with adjuvant chemotherapy post-surgery and is currently disease free. Primary renal PNET is a distinct and rare entity. This tumor is very aggressive with low survival rate, even with a multi-disciplinary approach. We reported the case because it is rare in children, poses diagnostic challenges, is aggressive in behaviour and responds poorly to treatment.
尤因肉瘤/原始神经外胚层肿瘤(PNET)是一种高级别恶性肿瘤,通常累及胸部骨骼。肾脏原发性尤因肉瘤/PNET极为罕见;它常见于年轻人,儿童中鲜有报道。在此,我们描述一例10岁女孩的肾PNET病例,该女孩因血尿和腹部肿块前来我院就诊。计算机断层扫描显示右肾有一个巨大肿块。对该肿块进行计算机断层扫描引导下穿刺,显示为小蓝圆细胞瘤的细胞形态学特征。患者接受了右肾根治性切除术。组织病理学检查及补充免疫组化确诊为PNET。她术后一直在接受辅助化疗,目前无疾病迹象。原发性肾PNET是一种独特且罕见的实体。即使采用多学科方法治疗,这种肿瘤也极具侵袭性,生存率低。我们报告该病例是因为它在儿童中罕见,存在诊断挑战,行为侵袭性强且对治疗反应不佳。