Hypertrophic olivary degeneration associated with bilateral vocal cord adductor dystonia

Abstract

Background Hypertrophic olivary degeneration (HOD) is a rare condition caused by lesions within the dentato-rubro-olivary pathway, resulting in ocular nystagmus and palatal myoclonus (oculopalatal tremor) but not usually dystonia. Dystonia is an uncommon association, and we present the first reported association of hypertrophic olivary degeneration with bilateral vocal cord dystonia. Case presentation A 33 year old male presented initially with acute hydrocephalus on the background of previous ventriculoperitoneal (VP) shunting for previously treated medulloblastoma. After revision of the VP shunt, the patient developed progressive hiccups and stridor leading to respiratory failure requiring intubation. Ocular pendular nystagmus and palatal myoclonus at 3 Hz was observed. Flexible nasendoscopy (FNE) demonstrated bilateral tonic adduction of the vocal folds with 3 Hz coarse supraglottic, pharyngeal and palatal rhythmic myoclonus. MRI imaging demonstrated T2 hyperintensity within the bilateral inferior olivary nuclei consistent with stage 3 radiological HOD. Conclusions Dystonia is a rarely reported phenomenon in HOD but is not unexpected with the inferior olivary nucleus implicated in dystonic disorders. We report the association of HOD with bilateral vocal cord adductor dystonia, a potentially life threatening condition.

Post-traumatic hypertrophic olivary degeneration associated with Holmes tremor: clinical-imaging correlation

“…Sus causas más frecuentes, corresponden a noxas unilaterales o bilaterales en el tronco encefálico y/o cerebelo, tales como: hemorragia, isquemia, neoplasia o trauma, las cuales pueden ser identificadas en la Resonancia Magnética Cerebral (RMC). La DOH implica gran variabilidad de presentaciones clínicas, desde cuadros asintomáticos a temblor palatino, mioclonías oculares, distonías, temblor dentado-rubral o de Holmes (TH) [3][4][5][6][7][8][9] .…”