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伪装成尤因肉瘤/原始神经外胚层肿瘤的恶性周围神经鞘瘤

Malignant Peripheral Nerve Sheath Tumors Masking as Ewing Sarcoma/Primitive Neuroectodermal Tumors.

作者信息

Shaikh Marwan, Rana Fauzia

机构信息

University of Florida College of Medicine Jacksonville, 7651 Gate Parkway #1211, Jacksonville, FL 32256, USA.

Division of Hematology and Medical Oncology, University of Florida College of Medicine Jacksonville, UF Hematology/Oncology at Pavilion, 4th Floor North, Pavilion, 555 West 8th Street, Jacksonville, FL 32209, USA.

出版信息

World J Oncol. 2013 Jun;4(3):161-164. doi: 10.4021/wjon661w. Epub 2013 Jul 15.

Abstract

Malignant peripheral nerve tumors, a small subset of soft tissue sarcomas, provide a unique diagnostic challenge. Although they may arise from peripheral nerves or from cells associated with nerve sheaths, malignant peripheral nerve tumors often present with diverse immunohistochemical features similar to those of other tumors. These features make MPNSTs difficult to diagnose and classify. We present a case of a 26-year-old female presenting with a rapidly growing soft tissue mass. The mass was excised and immunohistological staining suggested a Ewing's sarcoma/Primitive neuroectodermal tumor. Confirmational studies did not confirm this diagnosis and upon further review, the diagnosis was changed to a malignant peripheral nerve sheath tumor. We reviewed this case in the setting of the reported literature concerning MPNSTs with focus on the epidemiologic, diagnostic, and immunohistologic features that distinguish this tumor from other similar malignancies.

摘要

恶性外周神经肿瘤是软组织肉瘤中的一个小分支,带来了独特的诊断挑战。尽管它们可能起源于外周神经或与神经鞘相关的细胞,但恶性外周神经肿瘤通常呈现出与其他肿瘤相似的多种免疫组化特征。这些特征使得恶性外周神经鞘瘤难以诊断和分类。我们报告一例26岁女性患者,其出现快速生长的软组织肿块。该肿块被切除,免疫组织化学染色提示为尤因肉瘤/原始神经外胚层肿瘤。确诊研究未证实这一诊断,经进一步复查,诊断改为恶性外周神经鞘瘤。我们结合已报道的有关恶性外周神经鞘瘤的文献来回顾该病例,重点关注将此肿瘤与其他相似恶性肿瘤区分开来的流行病学、诊断和免疫组化特征。

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