青年多形性低级别神经上皮肿瘤:罕见肿瘤及文献复习

IF 0.9 Q4 ONCOLOGY
Ali H. Palejwala, Christen M. O’Neal, Michael R Quinton, J. Battiste, J. Peterson, I. Dunn
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引用次数: 7

摘要

多形性青年低级别神经上皮肿瘤(PLNTY)是一种最近描述的低级别神经表皮肿瘤,具有浸润性生长模式和CD34免疫阳性的少突胶质细胞样细胞。相关的组织学和分子检测结果对于正确诊断PLNTY至关重要,因为它的组织学外观与少突胶质瘤相似,并且与其他低度癫痫相关肿瘤(LEAT)有共同的遗传异常。在本病例报告中,我们描述了一名患有顽固性癫痫的31岁女性,经组织病理学和分子检测,发现其颞部有肿块,并被诊断为PLNTY。我们描述了与该患者癫痫和肿瘤学结果相关的放射学、组织学和遗传学特征。然后,我们将这些特征和结果与文献中描述的PLNTY的其他病例进行比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polymorphous low-grade neuroepithelial tumor of the young: Rare tumor and review of the literature
Polymorphous low-grade neuroepithelial tumor of the young (PLNTY) is a recently described low-grade neuroepithelial tumor with an infiltrative growth pattern and oligodendrocyte-like cells that are CD34 immunopositive. Correlating histology and results from molecular testing is critical to correctly diagnosing PLNTY, as its histologic appearance is similar to oligodendrogliomas and shares genetic abnormalities common to other low-grade epilepsy associated tumors (LEATs). In this case report, we describe a 31-year-old female with intractable epilepsy found to have a temporal mass and diagnosed with PLNTY after histopathologic and molecular testing. We describe the radiographic, histologic, and genetic features in relation to the epileptic and oncologic outcomes for this patient. Then, we compare these features and outcomes to other cases of PLNTY described in the literature.
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来源期刊
Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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