Hypertrophic Olivary Degeneration: A Neurosurgical Point of View

Carlos Henrique Carvalho, Hubert Kimmig, William Omar Contreras Lopez, Manfred Lange, Reinhard Oeckler

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Hypertrophic olivary degeneration (HOD) is a rare form of transsynaptic degeneration characterized by hypertrophy of the inferior olivary nucleus situated in the olivary body, part of the medulla oblongata, representing a major source of input to the cerebellum. HOD typically results from focal lesions interrupting connections from the inferior olive within the dentato-rubro-olivary pathway, a region also known as the triangle of Guillain-Mollaret (TGM) (red nucleus, inferior olivary nucleus, and contralateral dentate nucleus). Clinically, HOD presents classically as palatal tremor and can include dentatorubral tremor and/or ocular myoclonus. The pathologic changes associated with HOD feature radiologic changes with the inferior olivary nucleus appearing larger and increasing its T2-weighted signal intensity on magnetic resonance images. HOD is commonly managed with pharmacotherapy but may require surgical intervention in extreme cases. HOD has been found to develop as a consequence of any injury that disrupts the TGM pathways (e.g., pontine cavernoma).These findings highlight the critical importance of a thorough knowledge of TGM anatomy to avoid secondary HOD. We present a patient who developed HOD secondary to resection of a tectal plate cavernous malformation and review the literature with an emphasis on the current knowledge of this disorder.

Original languageEnglish
Pages (from-to)59-62
Number of pages4
JournalJournal of Neurological Surgery, Part A: Central European Neurosurgery
Volume77
Issue number1
DOIs
StatePublished - 20 Nov 2015
Externally publishedYes

Keywords

  • hypertrophic olivary degeneration (HOD)
  • neurosurgical intervention
  • symptomatic tremor
  • triangle of Guillain-Mollaret (TGM)

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