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肾尤文肉瘤/原始神经外胚层肿瘤:一例报告及文献复习

Renal Ewing's sarcoma/primitive neuroectodermal tumor: a case report and literature review.

作者信息

Liu C, Cui L G, Wang H L

机构信息

Department of Ultrasound, Peking University Third Hospital, Beijing 100191, China.

Department of Radiology, Peking University Third Hospital, Beijing 100191, China.

出版信息

Beijing Da Xue Xue Bao Yi Xue Ban. 2017 Oct 18;49(5):919-923.

Abstract

Ewing's sarcoma/primitive neuroectodermal tumor (EWS/PNET) in the kidney is a rare but high-grade malignant tumor that affects predominantly elder children and adolescents. Patients mostly present with nonspecific symptoms such as abdominal pain and gross hematuria. Since EWS/PNET has a rapid clinical progression with early metastasis and death, it is essential to make an accurate and early diagnosis. Once diagnosed, multimodality treatment, including radical surgery combined with adjuvant chemotherapy, and radiotherapy if necessary, is recommended. Unfortunately, there are no characteristic signsthat have been described in ultrasonography or any other imaging modalities so far. The diagnosis of EWS/PNET is now based on a classical histological and immunohistochemical investigation complemented by a demonstration of specific chromosomal changes. Strong immunoreactivity to CD99 is ubiquitous, and t(11;22) translocation is seen in approximately 90% of EWS/PNET. Herein, we report a patient with such condition. The patient was a young woman, and she presented with sudden right flank pain clinically. Ultrasonography revealed a large heterogeneous mass in the lower pole of her right kidney. The tumor compressed the renal pelvis and led to upper pole caliectasis. Color Doppler demonstrated blood flow with a pulsatile arterialized waveform within the mass. The patient received radical nephrectomy with right renal vein and vena cava thrombectomy. A search for other sites of tumor involvement yielded negative results. And six cycles of chemotherapy were sequentially performed. The diagnosis of EWS/PNET was confirmed based on primitive small round cell histology and characteristic immunohistochemical results. She was still alive with no evidence of recurrence five years after initial diagnosis. We would like to point out that ultrasound is still a useful method for initial assessment, and ultrasound-guided fine needle aspiration may play an important role in determining preoperative diagnosis.

摘要

肾脏尤文肉瘤/原始神经外胚层肿瘤(EWS/PNET)是一种罕见但高度恶性的肿瘤,主要影响大龄儿童和青少年。患者大多表现为腹痛和肉眼血尿等非特异性症状。由于EWS/PNET临床进展迅速,早期即发生转移并导致死亡,因此准确早期诊断至关重要。一旦确诊,建议采取多模式治疗,包括根治性手术联合辅助化疗,必要时进行放疗。不幸的是,目前超声检查或任何其他影像学检查方法均未发现其特征性表现。EWS/PNET的诊断目前基于经典的组织学和免疫组织化学检查,并辅以特定染色体改变的检测。对CD99的强免疫反应性普遍存在,约90%的EWS/PNET可见t(11;22)易位。在此,我们报告一例患有该疾病的患者。该患者为年轻女性,临床上表现为突发右侧腰痛。超声检查显示右肾下极有一个大的不均匀肿块。肿瘤压迫肾盂,导致上极肾盏扩张。彩色多普勒显示肿块内有搏动性动脉化血流波形。患者接受了根治性肾切除术及右肾静脉和腔静脉血栓切除术。对其他肿瘤累及部位的检查结果为阴性。随后进行了六个周期的化疗。根据原始小圆形细胞组织学和特征性免疫组织化学结果确诊为EWS/PNET。初次诊断五年后,她仍然存活,无复发迹象。我们想指出,超声仍然是初步评估的有用方法,超声引导下细针穿刺在确定术前诊断方面可能发挥重要作用。

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