Gupta Sahil, Majumder Kaustav, Chahal Anurag, Saini Ashish K, Gupta Arjun
University of Texas Southwestern Medical Centre, Dallas, Tex., USA.
Curr Urol. 2016 Feb;9(1):47-50. doi: 10.1159/000442851. Epub 2016 Feb 10.
Primitive neuroectodermal tumors (PNET) are an aggressive group of small round cell tumors usually arising in the nervous system and affecting children. They have a tendency for local invasion, distant spread and formation of tumor thrombi. The kidney is a rare primary location for these tumors. Outcomes are frequently poor due to late diagnosis (Wilms tumor is a more common tumor in this population) and early spread. Immunohistochemistry is invaluable in making the diagnosis of PNET. We report a case of a primary renal PNET with extensive tumor thrombus into the inferior vena cava, and lung metastasis in a pediatric patient, and its successful management. Our 14-year-old patient with renal PNET was managed with radical nephrectomy, thrombectomy and chemotherapy and remains disease free to date. The diagnosis of renal PNETs should be considered in young adult patients who present with aggressive renal masses at initial presentations. Despite its aggressive nature, good outcomes can be achieved by a multimodality therapeutic strategy.
原始神经外胚层肿瘤(PNET)是一组侵袭性较强的小圆细胞肿瘤,通常发生于神经系统,多见于儿童。它们易于局部浸润、远处转移并形成肿瘤血栓。肾脏是这些肿瘤罕见的原发部位。由于诊断较晚(该人群中威尔姆斯瘤更为常见)且早期发生转移,其预后通常较差。免疫组织化学对于PNET的诊断具有重要价值。我们报告了一例小儿原发性肾PNET病例,肿瘤广泛形成血栓并延伸至下腔静脉,同时伴有肺转移,以及对该病例的成功治疗。我们14岁的肾PNET患者接受了根治性肾切除术、血栓切除术及化疗,至今无疾病复发。对于初诊时出现侵袭性肾肿块的年轻成年患者,应考虑肾PNET的诊断。尽管其具有侵袭性,但通过多模式治疗策略可取得良好疗效。