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原发性皮肤尤因肉瘤/原始神经外胚层肿瘤:首例经细针穿刺抽吸细胞学诊断病例报告

Primary cutaneous ewing's sarcoma/primitive neuroectodermal tumor: report of the first case diagnosed on aspiration cytology.

作者信息

Kalra Sonali, Gupta Ruchika, Singh Sompal, Gupta Kusum, Kudesia Madhur

机构信息

Department of Pathology, Hindu Rao Hospital, Malka Ganj, Delhi, India.

出版信息

Acta Cytol. 2010 Mar-Apr;54(2):193-6. doi: 10.1159/000325008.

Abstract

BACKGROUND

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.

CASE

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.

CONCLUSION

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.

摘要

背景

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。

病例

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。

结论

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。

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