Atypical Teratoid Rhabdoid Tumor of the Pineal Region in a 33-Month-Old Child: A Case Report

MICHELLE ALEJANDRA MACIAS GRAGEDA, Jorge Andres Montenegro Salcedo, Jorge Alejandro Rodríguez Ruiz, Alfonso Sánchez Terán, Oscar García Gonzalez, Edgard Lozada Hernandez
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Abstract

Purpose: The present article describes a patient with an atypical teratoid/rhabdoid tumor of the pineal region and a literature review about this uncommon pathology. Methods: Literature review about Atypical Teratoid Rhabdoid Tumor between March and July of 2023 using 7 databases: Web of Science, Pubmed, Cochrane Library, SCOPUS, Science Direct, Clinical key and Medscape. Clinical features: A 33-month-old patient with an Atypical Teratoid Rhabdoid Tumor (ATRT) of the pineal region presented headache, VI cranial nerve paralysis, bilateral ataxia and loss of sphincters control during 3 months. Intervention: Endoscopic ventriculostomy with biopsy that reported ATRT. Conclusions: Recent statistics show that this tumor has been underdiagnosed throughout the time and evaluation of surgical material by a neuropathologist is required for its correct diagnosis.
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33月龄儿童松果体区非典型畸胎体样横纹肌样肿瘤1例报告
目的:本文报道一例不典型的松果体区畸胎瘤/横纹肌样瘤,并对这种罕见的病理进行文献回顾。方法:采用Web of Science、Pubmed、Cochrane Library、SCOPUS、Science Direct、Clinical key、Medscape等7个数据库,对2023年3 - 7月关于非典型畸胎体横纹肌样肿瘤的文献进行综述。临床特征:一例33个月大的松果体区非典型畸胎体横纹肌瘤(ATRT)患者,在3个月内出现头痛、脑神经麻痹、双侧共济失调和括约肌控制丧失。干预:内窥镜脑室造口术和活检报告ATRT。结论:最近的统计数据显示,该肿瘤一直被误诊,需要神经病理学家对手术材料进行评估才能正确诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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