Progression of a pontine cavernous malformation and delayed bilateral hypertrophic olivary degeneration: illustrative case

BACKGROUND: Hypertrophic olivary degeneration (HOD) is a rare form of transsynaptic degeneration caused by disruption of the dentato-rubro-olivary pathway (Guillain-Mollaret triangle). It is most described following surgical intervention or acute hemorrhagic injury affecting that pathway. However, longitudinal imaging documenting the natural progression of HOD in patients with brainstem cerebral cavernous malformations (CCMs) remains sparsely described at the individual patient level. OBSERVATIONS: The authors present the case of a 70-year-old woman with a pontine CCM followed longitudinally over 4 years. Initial imaging demonstrated a right-sided pontine lesion with unilateral HOD in the absence of symptoms. Over time, the CCM enlarged and extended across the midline, coinciding with the development of bilateral HOD and delayed onset of gait imbalance and palatal myoclonus. No surgical intervention was performed. LESSONS: In this case, the radiographic evolution from unilateral to bilateral involvement occurred concurrently with the delayed clinical manifestation of HOD. https://thejns.org/doi/10.3171/CASE26577.

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Journal
Journal of Neurosurgery Case Lessons
Published
2026-09-14
DOI
https://doi.org/10.3171/case26577
Primary Topic
Glycogen Storage Diseases and Myoclonus
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article
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article

Progression of a pontine cavernous malformation and delayed bilateral hypertrophic olivary degeneration: illustrative case

Kelly D. Flemming, Stephen Graepel, Giuseppe Lanzino, Delal Bektas
Journal of Neurosurgery Case Lessons
Glycogen Storage Diseases and Myoclonus
article

Progression of a pontine cavernous malformation and delayed bilateral hypertrophic olivary degeneration: illustrative case

Kelly D. Flemming, Stephen Graepel, Giuseppe Lanzino, Delal Bektas
article en

Abstract

BACKGROUND: Hypertrophic olivary degeneration (HOD) is a rare form of transsynaptic degeneration caused by disruption of the dentato-rubro-olivary pathway (Guillain-Mollaret triangle). It is most described following surgical intervention or acute hemorrhagic injury affecting that pathway. However, longitudinal imaging documenting the natural progression of HOD in patients with brainstem cerebral cavernous malformations (CCMs) remains sparsely described at the individual patient level. OBSERVATIONS: The authors present the case of a 70-year-old woman with a pontine CCM followed longitudinally over 4 years. Initial imaging demonstrated a right-sided pontine lesion with unilateral HOD in the absence of symptoms. Over time, the CCM enlarged and extended across the midline, coinciding with the development of bilateral HOD and delayed onset of gait imbalance and palatal myoclonus. No surgical intervention was performed. LESSONS: In this case, the radiographic evolution from unilateral to bilateral involvement occurred concurrently with the delayed clinical manifestation of HOD. https://thejns.org/doi/10.3171/CASE26577.

Journal of Neurosurgery Case LessonsVol. 12(11)
Mayo Clinic (US), University Hospital of Zurich (CH)
Good health and well-being
Openalex Percentile: Top 10%
Glycogen Storage Diseases and Myoclonus
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Progression of a pontine cavernous malformation and delayed bilateral hypertrophic olivary degeneration: illustrative case — Kelly D. Flemming, Stephen Graepel, et al. · Journal of Neurosurgery Case Lessons (2026) | TGRS Research Map | TGRS