Clinical Service of Pathology, Department of Pathology, "Sf. Apostol Andrei" Emergency County Hospital, 900591 Constanta, Romania.
Center for Research and Development of the Morphological and Genetic Studies of Malignant Pathology, "Ovidius" University of Constanta, 900591 Constanta, Romania.
Curr Oncol. 2022 Jul 28;29(8):5316-5323. doi: 10.3390/curroncol29080422.
Giant cell glioblastoma is a rare tumor entity of IDH-wildtype glioblastoma. It is usually found in the pediatric population. We describe a particular case of a female patient diagnosed histopathologically with giant cell glioblastoma, who had two recurrences in different lobes of the same cerebral hemisphere, despite positive prognostic factors and appropriate treatment. We performed an immunohistochemical characterization of giant cell glioblastoma as well as an analysis of its aggressiveness using the cytogenetic markers TP53, CDKN2A, and TP73 using the FISH technique. The clinical picture was inconsistant, the suspicion being completely different initially. Paraclinical examination and imaging initially suggested a metastasis to the insular lobe. After surgery, histopathological and immunohistochemical examinations were the basis for the diagnosis. Despite the prognostic factors known so far in the literature, the aggressiveness denoted by multiple relapses and morphogenetic tests particularizes the case and improves the literature by bringing new information about this rare neoplasm of the central nervous system.
巨细胞胶质母细胞瘤是一种罕见的 IDH 野生型胶质母细胞瘤肿瘤实体。它通常发生在儿科人群中。我们描述了一例女性患者的特殊病例,该患者经组织病理学诊断为巨细胞胶质母细胞瘤,尽管存在阳性预后因素和适当的治疗,但在同一大脑半球的不同叶中发生了两次复发。我们对巨细胞胶质母细胞瘤进行了免疫组织化学特征分析,并使用 FISH 技术分析了其细胞遗传学标志物 TP53、CDKN2A 和 TP73 的侵袭性。临床症状不一致,最初的怀疑完全不同。最初,临床检查和影像学检查提示岛叶转移。手术后,组织病理学和免疫组织化学检查是诊断的基础。尽管目前已知文献中的预后因素,但多次复发和形态发生测试所表示的侵袭性使该病例具有特殊性,并通过提供有关这种中枢神经系统罕见肿瘤的新信息来完善文献。