Kalra Sonali, Gupta Ruchika, Singh Sompal, Gupta Kusum, Kudesia Madhur
Department of Pathology, Hindu Rao Hospital, Malka Ganj, Delhi, India.
Acta Cytol. 2010 Mar-Apr;54(2):193-6. doi: 10.1159/000325008.
Extraskeletal Ewing's sarcoma (ES) was first recognized as a soft tissue tumor in 1975. Primacy cutaneous occurrence of Ewing's sarcoma/primitive neuroectodermnal tumor (ES/PNET) has been reported in only 31 cases so far. To the best of our knowledge, there is no report of preoperative cytologic diagnosis of cutaneous ES/PNET in the available literature except for this one.
A young adult presented with a recurrent swelling on the medial aspect of the left leg that had been present for the past 5 years. Fine needle aspiration cytology yielded cellular smears showing a small round cell tumor. Immunostaining on cell block material showed positivity for CD99, S-100 protein and neuron-specific enolase. A cytologic diagnosis of primary cutaneous ES/PNET was made. Local excision was performed, and the patient was well after 2 years of follow-up.
Primary cutaneous ES/PNET is a rare cutaneous tumor with a favorable clinical outcome. It can be diagnosed on cytology; however, immunocytochemistry is mandatory for differentiation from other small round cell tumors.
骨外尤因肉瘤(ES)于1975年首次被确认为一种软组织肿瘤。原发性皮肤尤因肉瘤/原始神经外胚层肿瘤(ES/PNET)迄今为止仅报道了31例。据我们所知,除本文外,现有文献中尚无关于皮肤ES/PNET术前细胞学诊断的报道。
一名年轻成人,左腿内侧反复出现肿胀,已持续5年。细针穿刺细胞学检查获得的细胞涂片显示为小圆形细胞肿瘤。细胞块材料的免疫染色显示CD99、S-100蛋白和神经元特异性烯醇化酶呈阳性。做出了原发性皮肤ES/PNET的细胞学诊断。进行了局部切除,患者经过2年随访情况良好。
原发性皮肤ES/PNET是一种罕见的皮肤肿瘤,临床预后良好。它可以通过细胞学诊断;然而,免疫细胞化学对于与其他小圆形细胞肿瘤进行鉴别是必不可少的。