Vanishing Contrast Enhancement of a Diffuse Midline Glioma.

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY
Neuropathology Pub Date : 2025-02-19 DOI:10.1111/neup.70002
Charles Champeaux Depond, Philippe Metellus, Emmanuel Gross, Romain Appay
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Abstract

Diffuse midline glioma, is a highly aggressive deep-seated glioma whose diagnosis must be confirmed through histopathological analysis of stereotactic biopsies. Hemorrhagic complications after intracranial biopsies may occur, potentially leading to severe neurological sequelae or significantly altering the outcome. A 55-year old male with no significant medical history presented to the local emergency department with 4 days of diplopia. A magnetic resonance imaging (MRI) confirmed the presence of tumor whose characteristics were highly suggestive of a high-grade infiltrating causing blocked hydrocephalus. As no safe resection was achievable, a third ventriculostomy followed by an endoscopic biopsy of the tumor was performed. Unfortunately, the procedure was complicated by an massive intraventricular bleeding of the tumor and, the tiny tumor specimens collected were not contributive. Fortunately, the patient survived and, his clinical state slowly improved. Follow up MRIs depicted a progressive regression of the tumor. As such a wait and see policy was preferred over a chemoradiotherapy. Ultimately, the gadolinium enhancement totally vanished. Unfortunately, 27 months after the initial presentation, he presented with a quick neurological worsening with severe hemiparesis and seizures for which cerebral imaging showed a malignant-looking deep-situated unresectable brain tumor. A second biopsy was performed without any specific complication. The histopathological examination of the tumor revealed a high-grade glial tumor characterized by hypercellularity, marked atypia, mitosis, microvascular proliferation, and areas of necrosis with positive H3 p.K28M nuclear staining in combination with the loss of nuclear H3 p.K28me3. He was referred for best supportive care and, died 29.6 months after the initial presentation. To our knowledge, this is the first report of the gadolinium enhancement of a diffuse midline glioma H3 K27-altered.

弥漫性中线胶质瘤造影增强消失。
弥漫性中线胶质瘤是一种高度侵袭性的深部胶质瘤,其诊断必须通过立体定向活检的组织病理学分析来证实。颅内活检后可能出现出血性并发症,可能导致严重的神经系统后遗症或显著改变结果。55岁男性,无明显病史,因复视4天就诊于当地急诊科。磁共振成像(MRI)证实肿瘤的存在,其特征高度提示高度浸润导致脑积水阻塞。由于无法实现安全切除,因此进行了第三次脑室造口术,随后进行了肿瘤的内窥镜活检。不幸的是,由于肿瘤的大量脑室内出血,手术变得复杂,而且收集到的微小肿瘤标本也没有帮助。幸运的是,病人活了下来,他的临床状况慢慢好转。后续mri显示肿瘤逐渐消退。因此,观望政策优于放化疗。最终,钆增强完全消失了。不幸的是,在初次发病27个月后,患者出现神经系统快速恶化,伴有严重偏瘫和癫痫发作,脑成像显示深部恶性肿瘤,不可切除。第二次活检没有任何特殊并发症。肿瘤的组织病理学检查显示为高级别胶质肿瘤,其特征为细胞增生、明显的异型性、有丝分裂、微血管增生和坏死区域,H3 p.K28M核染色阳性,并伴有细胞核H3 p.K28me3缺失。他接受了最好的支持治疗,在初次就诊后29.6个月死亡。据我们所知,这是第一次报道弥漫性中线胶质瘤H3 k27改变的钆增强。
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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来源期刊
Neuropathology
Neuropathology 医学-病理学
CiteScore
4.10
自引率
4.30%
发文量
105
审稿时长
6-12 weeks
期刊介绍: Neuropathology is an international journal sponsored by the Japanese Society of Neuropathology and publishes peer-reviewed original papers dealing with all aspects of human and experimental neuropathology and related fields of research. The Journal aims to promote the international exchange of results and encourages authors from all countries to submit papers in the following categories: Original Articles, Case Reports, Short Communications, Occasional Reviews, Editorials and Letters to the Editor. All articles are peer-reviewed by at least two researchers expert in the field of the submitted paper.
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