Adult-onset opsoclonus-myoclonus-ataxia syndrome as a manifestation of brazilian lyme disease-like syndrome: a case report and review of literature

• Main Authors: Angelina Maria Martins Lino, Raphael Ribeiro Spera, Fernando Peixoto Ferraz de Campos, Christian Henrique de Andrade Freitas, Márcio Ricardo Taveira Garcia, Leonardo da Costa Lopes, Aleksander Snioka Prokopowitsch
• Format: Article
• Language: English
• Published: University of São Paulo 2014-03-01
• Series: Autopsy and Case Reports
• Subjects: Opsoclonus-Myoclonus Syndrome; Lyme Neuroborreliosis; Borrelia burgdorferi.
• Online Access: http://www.revistas.usp.br/autopsy/article/view/81208

Described in 1962, the opsoclonus-myoclonus-ataxia syndrome (OMAS) is a rare, neurologically debilitating disorder with distinct characteristics that may begin in childhood or adult life. Although many cases remain without etiological diagnosis, others are related to neoplasms and infectious diseases. We report a 41-year-old previously healthy male with an 8-day history of headache, vertigo, nausea, vomiting, and nystagmus. After a normal brain computed tomography and lymphocytic pleocytosis in cerebral spinal fluid (CSF), intravenous acyclovir therapy was initiated in the emergency room. On the third day of hospitalization, the diagnosis of OMAS was made based on the presence of chaotic and irregular eye movements, dysarthric speech, gait instability, generalized tremor, and myoclonic jerks. In the face of his neurological worsening, ampicillin followed by nonspecific immunotherapy (methylprednisolone and intravenous immunoglobulin) was prescribed, with mild clinical improvement. After a thorough laboratory workup, the definite diagnosis of neuroborreliosis was established and ceftriaxone (4 g/daily/3wks) and doxycycline (200 mg/day/2 mo) was administered. Toward the end of the ceftriaxone regimen, the neurologic signs substantially improved. We believe this to be the first case description of OMAS as clinical presentation of Brazilian Lyme disease-like syndrome (Baggio-Yoshinari syndrome).