Che Shao-Min, Cao Pei-Long, Chen Hong-Wei, Liu Zi, Meng Du
Department of Radiation Oncology, First Affiliated Hospital, Xi'an Jiaotong University School of Medicine, Xi'an, 710061, China.
J Obstet Gynaecol Res. 2013 Mar;39(3):746-9. doi: 10.1111/j.1447-0756.2012.02019.x. Epub 2012 Oct 29.
Ewing sarcomas/peripheral primitive neuroectodermal tumors (ES/pPNET) are extremely rare in the vulva. A review of the literature reveals only 14 previously reported possible cases. Here we reported a case of primary extraskeletal Ewing's sarcoma (EES) of the vulva in a 37-year-old woman. Characteristic histologic features of ES/pPNET were present in this case, including a monomorphic population of small round blue cells with cytoplasmic glycogen confirmed by periodic acid-Schiff, membrane staining with CD99 and nuclear staining with FLI-1. After surgery, the patient was found to have pulmonary metastasis and then received six cycles of polychemotherapy. She is still alive with stable disease after 1 year of follow up. Our findings underline the crucial role of immunohistochemical techniques in the differential diagnosis of small round cell tumors in these unusual locations. We also give a summary about the clinical and pathological features of the primary ES/pPNET in the vulva reported previously in the literature.
尤因肉瘤/外周原始神经外胚层肿瘤(ES/pPNET)在外阴极为罕见。文献回顾显示,此前仅报道过14例可能的病例。在此,我们报告了一例37岁女性外阴原发性骨外尤因肉瘤(EES)。该病例具有ES/pPNET的典型组织学特征,包括单形性的小圆形蓝色细胞群,经高碘酸希夫染色证实有细胞质糖原,CD99膜染色及FLI-1核染色阳性。手术后,患者被发现有肺转移,随后接受了六个周期的多药化疗。随访1年后,她仍存活且病情稳定。我们的研究结果强调了免疫组化技术在这些不寻常部位小圆形细胞肿瘤鉴别诊断中的关键作用。我们还总结了文献中此前报道的外阴原发性ES/pPNET的临床和病理特征。