A Case of Diffuse Multicentric Metachronous Astrocytoma of Temporoinsular and Intramedullary Location

J. Torres, G. Botella, Antonio Selfa Rodríguez, La Larrazabal, Julia Casado Ruiz, Miguel Ángel Arráez Sánchez
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Abstract

Multiple gliomas are rare glial tumors with a histology that is typically consistent with high-grade gliomas. A distinction is made between multifocal and multicentric gliomas according to criteria of anatomical continuity, as well as between synchronous and metachronous gliomas according to chronological time of onset. We present the case of a professional saxophonist with a left temporoinsular lesion who underwent awake craniotomy with monitoring of verbal and musical ability as well as primary sensory and motor cortices. Histopathological study revealed an isocitrate dehydrogenase 1 (IDH)-mutant diffuse astrocytoma. After 4 years of complete oncological remission, the patient developed impaired proprioception in all four extremities. An intramedullary lesion was detected at the level of C4 consistent with an IDH wild-type diffuse astrocytoma. We highlight the singularity of this case as it involved two low-grade glial lesions, separated in time (metachronous) and location (multicentric), as well as genetic differences between both lesions (IDH mutant and wild type).
颞岛及髓内弥漫性多中心异时星形细胞瘤1例
多发性胶质瘤是一种罕见的神经胶质瘤,其组织学特征与高级别胶质瘤一致。根据解剖连续性的标准来区分多灶性和多中心胶质瘤,以及根据发病时间来区分同步性和异时性胶质瘤。我们提出的情况下,专业萨克斯风与左颞岛病变谁接受清醒开颅监测语言和音乐能力,以及初级感觉和运动皮层。组织病理学研究显示为异柠檬酸脱氢酶1 (IDH)突变的弥漫性星形细胞瘤。肿瘤完全缓解4年后,患者四肢本体感觉受损。在C4水平检测到髓内病变,与IDH野生型弥漫性星形细胞瘤一致。我们强调该病例的独特性,因为它涉及两个低级别胶质病变,在时间(异时性)和位置(多中心)上分离,以及两种病变(IDH突变型和野生型)之间的遗传差异。
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