第三脑室间变性少突胶质细胞瘤1例

Tamajyoti Ghosh, S. Dey
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引用次数: 0

摘要

背景和重要性:无定形少突胶质瘤(ODG)占所有儿童ODG的24%。ODG的平均发病年龄为12±6岁。它们最常见于额叶和颞叶;然而,脑室内ODG的罕见病例也有报道。最常见的是发生在侧脑室的前部。第三脑室ODG极为罕见,仅报告了少数侧脑室和第三脑室间变性ODG病例。ODG局部浸润到脑膜,很少有软脑膜扩散。因此,ODG形成了儿童脑室内肿瘤的鉴别诊断。病例介绍:我们报告一例15个月大的男性儿童,因梗阻性脑积水导致颅内压升高。患者在术前被检测为新冠肺炎RT–PCR(逆转录酶聚合酶链式反应)阳性,并接受了紧急右侧脑室腹膜(VP)分流。他的对比MRI(磁共振成像)大脑显示,在第三脑室有一个50×24×39mm的不均匀增强的肿块中心,并延伸到侧脑室和第四脑室,伴有脊髓滴状转移。对Ependymoma进行术前鉴别诊断,并在儿童从新冠肺炎中康复后进行最终手术。然而,他的活检标本病理学和免疫组织化学(IHC)提示为间变性少突胶质瘤,该儿童对化疗反应良好。结论:脑室ODG是一种极为罕见的儿童肿瘤。患者通常表现为梗阻性脑积水。对比MRI检查结果是非特异性的,有助于检测软脑膜向脊柱的扩散。IHC和染色体分析是重要的诊断和治疗预测工具。这些肿瘤尽管全部切除,但复发率高,预后差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Third Ventricle Anaplastic Oligodendroglioma: A Case Report
Background and Importance: Anaplastic Oligodendroglioma (ODG) constitutes 24% of all pediatric ODG. The mean age of presentation of ODG is 12±6 years. They are most common in frontal and temporal lobes; however, rare cases of intraventricular ODGs are reported. Most commonly they arise from the anterior part of lateral ventricles. Third ventricle ODG is extremely rare and only a few cases of lateral and third ventricle anaplastic ODG are reported. ODGs infiltrate locally to meninges and rarely have leptomeningeal spread. Thus, ODG forms a differential diagnosis of pediatric intraventricular tumor. Case Presentation: Here we present a case of a 15-month-old male child with raised intracranial pressure due to obstructive hydrocephalus. The patient was detected to be COVID-19 RT–PCR (Reverse Transcriptase Polymerase Chain Reaction) positive in the preoperative period and underwent emergency Right-sided Ventriculo Peritoneal (VP) shunt. His contrast MRI (Magnetic Resonance Imaging) Brain showed a 50×24×39 mm heterogeneously enhancing mass epicenter at third ventricle and extending to lateral and fourth ventricle with spinal drop metastasis. Preoperative differential diagnosis of Ependymoma was made and definitive surgery was done once the child recovered from COVID-19. However, his biopsy specimen pathology and Immunohistochemistry (IHC) were suggestive of anaplastic oligodendrogliomas and the child responded well to chemotherapy. Conclusion: Intraventricular ODG is an extremely rare pediatric tumor. Patients usually present with obstructive hydrocephalus. Contrast MRI findings are nonspecific and help in detecting leptomeningeal spread to the spine. IHC and chromosomal analysis are important diagnostic and treatment prognostication tools. These tumors have a high recurrence and poor prognosis despite gross total resection.
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CiteScore
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