Uchimura Masahiro, Araki Asuka, Eda Hirotake, Kimura Yoriyoshi, Hayashi Kentaro
Department of Neurosurgery, NHO Hamada Medical Center, 777-12 Asai-cho, Hamada-shi, Shimane, 697-0022, Japan.
Department of Neurosurgery, Shimane University Faculty of Medicine, Izumo, Shimane, Japan.
Brain Tumor Pathol. 2025 Sep 17. doi: 10.1007/s10014-025-00515-1.
A limited number of cases involving non-midline lesions have been documented in diffuse midline glioma (DMG), H3K27-altered, for which a definitive classification has yet to be developed. Additionally, no studies have investigated the temporal evolution of imaging features in diffuse non-midline gliomas. We herein report a case of DMG, H3K27-altered, initially presenting with a gliomatosis cerebri-like appearance, cystic lesions in the right frontal lobe, and progression toward the brainstem. Histopathological analysis and comprehensive genomic profiling indicated glioblastoma (GBM) or DMG, H3K27-altered. The patient was diagnosed with GBM because of imaging characteristics atypical for DMG; however, 9 months after the initial diagnosis, a pontine glioma emerged. This case indicates that DMG, H3K27-altered, may exhibit atypical characteristics, including non-midline cystic lesions, that can subsequently progress to pontine gliomas. Considering the limited therapeutic options available for this malignancy, the early recognition of such atypical presentations is crucial for achieving a timely and accurate diagnosis of DMG, H3K27-altered.
在H3K27改变的弥漫性中线胶质瘤(DMG)中,有少数涉及非中线病变的病例被记录下来,对此尚未形成明确的分类。此外,尚无研究调查弥漫性非中线胶质瘤影像学特征的时间演变情况。我们在此报告一例H3K27改变的DMG病例,该病例最初表现为大脑胶质瘤病样外观、右侧额叶囊性病变,并向脑干进展。组织病理学分析和综合基因组分析表明为胶质母细胞瘤(GBM)或H3K27改变的DMG。由于影像学特征不符合DMG,该患者被诊断为GBM;然而,在初次诊断9个月后,出现了桥脑胶质瘤。该病例表明,H3K27改变的DMG可能表现出非典型特征,包括非中线囊性病变,随后可能进展为桥脑胶质瘤。鉴于针对这种恶性肿瘤的治疗选择有限,早期识别此类非典型表现对于及时、准确诊断H3K27改变的DMG至关重要。