# Case Report: A case of diffuse midline glioma, H3 K27-altered presenting with long-segment spinal cord lesions

**Authors:** Chengcheng Lu, Songke Lu, Rongrong Li, Rui Pang, Ruijiao Zhao, Yao Cui, Jianguo Zhang, Wei Li, Huiqin Liu

PMC · DOI: 10.3389/fonc.2026.1658494 · Frontiers in Oncology · 2026-03-03

## TL;DR

This case report describes a rare brain tumor in a young adult that initially appeared as spinal cord lesions and was later diagnosed as diffuse midline glioma H3 K27-altered.

## Contribution

The report highlights the unusual spinal cord presentation of a rare pediatric-type glioma in an adult, aiding in clinical recognition.

## Key findings

- The patient presented with progressive quadriparesis and spinal cord lesions initially misdiagnosed as myelitis.
- MRI showed abnormal signals in the medulla oblongata and thoracic spinal cord, confirmed by biopsy as H3 K27-altered glioma.
- Despite treatment, the patient's condition worsened, leading to respiratory failure and death within 12 days of diagnosis.

## Abstract

Diffuse midline glioma H3 K27-altered is a subtype of pediatric-type diffuse high-grade gliomas, characterized as an infiltrative high-grade glioma involving midline structures with H3 K27 mutation. This clinically rare entity poses diagnostic challenges in the early stages and carries an extremely poor prognosis. We report a case of diffuse midline glioma H3 K27-altered, primarily manifesting as spinal cord lesions, and detail its clinical characteristics to enhance understanding of this disease entity. A 21-year-old male presented with “progressive quadriparesis over 7 months.” Seven months prior, he had developed bilateral lower limb weakness (grade II) following a cold. MRI at a local hospital revealed abnormal signals at T2–T5, diagnosed as “myelitis.” The disease progressed with lesion expansion despite treatment with glucocorticoid pulse therapy and intravenous immunoglobulin. The patient visited our hospital 7 months after the onset of the disease. At that time, the patient exhibited grade I muscle strength in the right upper limb and grade 0 in all other limbs, with sensory impairment below the neck. MRI revealed abnormal signals in the medulla oblongata and thoracic spinal cord. The patient received high-dose glucocorticoid pulse therapy again, but the symptoms did not improve despite treatment. The definitive diagnosis of diffuse midline glioma H3 K27-altered was established through spinal cord biopsy. The patient was discharged from the hospital due to respiratory failure 12 days post-diagnosis.

## Linked entities

- **Diseases:** diffuse midline glioma H3 K27-altered (MONDO:1060171), myelitis (MONDO:0002565)

## Full-text entities

- **Diseases:** myelitis (MESH:D009187), respiratory failure (MESH:D012131), Diffuse midline glioma (MESH:D005910), quadriparesis (MESH:D011782), lower limb weakness (MESH:D018908), spinal cord lesions (MESH:D013118), sensory impairment (MESH:D012678)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12992005/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12992005/full.md

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Source: https://tomesphere.com/paper/PMC12992005