Lisievici Antonia Carmen, Bohîlţea Roxana Elena, Berceanu Costin, Lisievici Mihai Gheorghe, Varlas Valentin, Grigoriu Corina, Vlădăreanu Emilia Maria, Georgescu Tiberiu-Augustin
Department of Pathology, "Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania.
Department of Obstetrics and Gynecology, "Carol Davila" University of Medicine and Pharmacy,Filantropia Clinical Hospital, Bucharest, Romania.
Curr Health Sci J. 2021 Oct-Dec;47(4):523-528. doi: 10.12865/CHSJ.47.04.07. Epub 2021 Dec 31.
Gangliogliomas are extremely rare central nervous tumors composed of an admixture of glial and neuroepithelial elements. Gangliogliomas mainly affect the temporal lobe and occur in the pediatric population. There are several controversies in the scientific literature regarding these tumors, which debuted with the exclusion of grade II gangliogliomas in the 2006 edition of the current World Health Organization (WHO) classification. The upcoming edition due in the last months of 2021 is not expected to include changes regarding the current classification of glio-neuronal tumors. This vision has led to a number of articles that have pushed for the reintroduction of this category. However, these articles support the reintroduction of this degree in terms of prognosis and evolution, without providing clear criteria for the inclusion of certain gangliogliomas in this category. On the other hand, there are uncertainties about the relationship of gangliogliomas with focal cortical dysplasia. The coexistence of the two entities, as well as their succession are occasionally encountered in practice and have led to numerous studies that have tried to clarify the relationship between them. The most common and most accessible element in routine practice is the immunoreactivity for CD34. Both entities express this marker, and dual lesions express the highest percentage of immunoreactivity for CD34. In this article, we study the expression of CD34 on a series of cases including both grade I gangliogliomas and anaplastic gangliogliomas diagnosed between 2011 and 2020 in a Neuropathology Unit in Bucharest Romania.
神经节胶质瘤是极为罕见的中枢神经系统肿瘤,由神经胶质和神经上皮成分混合组成。神经节胶质瘤主要累及颞叶,好发于儿童群体。关于这些肿瘤,科学文献中存在诸多争议,自2006年版世界卫生组织(WHO)分类中排除II级神经节胶质瘤起就有相关争议。预计将于2021年最后几个月发布的下一版分类预计不会对目前神经胶质-神经元肿瘤的分类做出改变。这种观点引发了一些主张重新引入该类别的文章。然而,这些文章在预后和演变方面支持重新引入该级别,但未提供将某些神经节胶质瘤纳入该类别的明确标准。另一方面,神经节胶质瘤与局灶性皮质发育异常之间的关系存在不确定性。在实际中偶尔会遇到这两种情况的共存及其先后出现,这引发了众多试图阐明它们之间关系的研究。常规实践中最常见且最易获取的要素是CD34的免疫反应性。这两种情况均表达该标志物,而双重病变中CD34免疫反应性的表达百分比最高。在本文中,我们研究了2011年至2020年间在罗马尼亚布加勒斯特一家神经病理学单位诊断的一系列包括I级神经节胶质瘤和间变性神经节胶质瘤病例中CD34的表达情况。