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弥漫性中线胶质瘤H3K27改变伴胸椎硬膜外转移:病例说明

Diffuse midline glioma H3K27-altered with thoracic epidural metastasis: illustrative case.

作者信息

Sumita Kan, Sawada Masahiro, Hattori Etsuko Yamamoto, Sano Noritaka, Takada Shigeki, Tanji Masahiro, Mineharu Yohei, Kikuchi Takayuki, Arakawa Yoshiki

机构信息

Department of Neurosurgery, Kyoto University Graduate School of Medicine, Kyoto, Kyoto, Japan.

Department of Artificial Intelligence in Healthcare and Medicine, Kyoto University Graduate School of Medicine, Kyoto, Kyoto, Japan.

出版信息

J Neurosurg Case Lessons. 2025 Jul 14;10(2). doi: 10.3171/CASE25249.

Abstract

BACKGROUND

Diffuse midline glioma (DMG) H3K27-altered is a newly recognized diffuse high-grade tumor entity in the 5th edition of the WHO classification of CNS tumors. Spinal extradural metastasis is extremely rare in patients with DMG H3K27-altered, while the occurrence of spinal intramedullary DMG, intradural dissemination, and osseous metastasis has been reported.

OBSERVATIONS

The authors report the case of a 6-year-old female presenting with acute-onset urinary retention and paraplegia, who was found to have a pontine DMG, an intradural mass at the level of T1-6, and an extradural lesion at T6-9. The thecal sac was severely compressed by the extradural mass; thus, a T6-9 laminectomy and extradural tumor resection were performed. After the procedure, an amelioration of weakness was observed. The patient was treated with radiotherapy to the spine. Pathology revealed an increase in chromatin, the proliferation of atypical cells, and microvascular proliferation. The H3K27 mutation was confirmed.

LESSONS

This case demonstrates an operative view in the metastasis of DMG H3K27-altered to the spinal epidural space without visceral or osseous metastasis. The possibility of spinal epidural metastasis and its surgical treatability should be considered if patients with DMG present spinal cord symptoms. https://thejns.org/doi/10.3171/CASE25249.

摘要

背景

H3K27改变的弥漫性中线胶质瘤(DMG)是《世界卫生组织中枢神经系统肿瘤分类》第5版中新近确认的一种弥漫性高级别肿瘤实体。H3K27改变的DMG患者发生脊柱硬膜外转移极为罕见,不过已有脊髓内DMG、硬膜内播散及骨转移发生的报道。

观察结果

作者报告了1例6岁女性患者,该患者急性起病,出现尿潴留和截瘫,检查发现患有桥脑DMG、T1-6水平的硬膜内肿块以及T6-9水平的硬膜外病变。硬膜外肿块严重压迫硬脊膜囊;因此,实施了T6-9椎板切除术及硬膜外肿瘤切除术。术后观察到肌无力有所改善。患者接受了脊柱放疗。病理检查显示染色质增多、非典型细胞增殖以及微血管增生。H3K27突变得到确认。

经验教训

本病例展示了H3K27改变的DMG转移至脊柱硬膜外间隙且无内脏或骨转移时的手术视野。如果DMG患者出现脊髓症状,应考虑脊柱硬膜外转移的可能性及其手术可治疗性。https://thejns.org/doi/10.3171/CASE25249

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