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首页> 外文期刊>Cureus. >Large Adult Spinal Diffuse Midline Histone H3 Lysine27-to-Methionine-Mutant Glioma With Intramedullary and Extramedullary Components Presenting With Progressive Hydrocephalus: A Case Report Highlighting Unique Imaging Findings and Treatment
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Large Adult Spinal Diffuse Midline Histone H3 Lysine27-to-Methionine-Mutant Glioma With Intramedullary and Extramedullary Components Presenting With Progressive Hydrocephalus: A Case Report Highlighting Unique Imaging Findings and Treatment

机译:大型成年脊髓扩散中线组蛋白H3赖氨酸27-甲硫氨酸 - 突变胶质胶质胶质胶质瘤,具有渐进性脑积水的髓内和蛋白质组分:案例报告突出了独特的成像结果和治疗

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摘要

Diffuse midline glioma with histone H3 lysine27-to-methionine mutation (H3 K27M mutation) is a rare, aggressive tumor that is designated as World Health Organization (WHO) grade IV regardless of histologic features. Preoperative diagnosis remains challenging due to limited evidence regarding distinctive clinical and imaging characteristics. We describe the case of a young woman who presented with progressively worsening headaches due to communicating hydrocephalus. MR imaging with contrast of the cervical and thoracic spine revealed diffuse leptomeningeal enhancement with focal areas of intramedullary and subarachnoid T2 hyperintensity and enhancement, suggestive of a potential infectious process. Intraoperatively, no epidural pathology was identified, and with the differential diagnosis remaining broad, a second procedure was conducted involving intradural exploration and biopsy of a lesion. This was then identified as a diffuse midline glioma with H3 K27M mutation. The nonfocal clinical presentation in the setting of communicating hydrocephalus?as well as the significant exophytic tumor growth and imaging findings made the initial diagnosis unique and challenging. This case, therefore, emphasizes the rare presentation of this tumor, and the need for further understanding of the clinical and imaging characteristics of this disease?as well as the need for effective therapeutics.
机译:弥漫性中线胶质瘤与组蛋白H3赖氨酸27-蛋氨酸突变(H3 K27M突变)是一种罕见的侵蚀性肿瘤,其被指定为世界卫生组织(WHO)IV级,无论组织学特征如何。由于有关独特的临床和影像学特征的证据有限,术前诊断仍然挑战。我们描述了一位年轻女性的案例,他们由于沟通脑积水而逐渐恶化。宫颈和胸椎脊柱的对比先生揭示了弥漫性百分之肌增强与髓内和蛛网膜瘤T2超强度和增强的焦点区域,提出了潜在的传染过程。术中,没有发现硬膜外病理学,并且随着差异的诊断宽容,进行了第二种程序,涉及病变的内部探测和活组织检查。然后将其鉴定为具有H3 K27M突变的弥漫性中线胶质瘤。在沟通脑积水环境中的非焦临床介绍?以及显着的突出肿瘤生长和成像结果使初步诊断独特和具有挑战性。因此,这种情况强调了这种肿瘤的罕见呈现,需要进一步了解这种疾病的临床和影像特征?以及有效治疗的需求。

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