弥漫性中线胶质瘤h3k27伴胸椎硬膜外转移:说明性病例。

Kan Sumita, Masahiro Sawada, Etsuko Yamamoto Hattori, Noritaka Sano, Shigeki Takada, Masahiro Tanji, Yohei Mineharu, Takayuki Kikuchi, Yoshiki Arakawa
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引用次数: 0

摘要

背景:弥漫性中线胶质瘤(Diffuse midline glioma, DMG) H3K27-altered是WHO第5版中枢神经系统肿瘤分类中新认定的弥漫性高级别肿瘤实体。在DMG h3k27改变的患者中,脊髓硬膜外转移极为罕见,而脊髓髓内DMG、硬膜内播散和骨转移的发生已被报道。观察:作者报告了一名6岁女性急性尿潴留和截瘫的病例,她被发现有脑桥DMG,硬膜内肿块在T1-6水平,硬膜外病变在T6-9。硬膜外肿块严重压迫硬膜囊;因此,我们进行了T6-9椎板切除术和硬膜外肿瘤切除术。手术后,观察到虚弱的改善。病人接受脊椎放射治疗。病理显示染色质增加,非典型细胞增生,微血管增生。H3K27突变被证实。经验:本病例展示了DMG h3k27转移到脊髓硬膜外腔的手术观点,没有内脏或骨转移。如果DMG患者出现脊髓症状,应考虑脊髓硬膜外转移的可能性及其手术治疗。https://thejns.org/doi/10.3171/CASE25249。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diffuse midline glioma H3K27-altered with thoracic epidural metastasis: illustrative case.

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.

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