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Published on: November 21, 2013
The movement disorder of adult opsoclonus
J N Caviness1, P A Forsyth, D D Layton
1Department of Neurology, Mayo Clinic, Scottsdale, Arizona 85259.
Abstract:
We present three cases of the adult opsoclonus-myoclonus syndrome in patients with systemic carcinoma. In addition to opsoclonus and myoclonus, other clinical components of the syndrome can include ataxia, tremor, gait and stance dysfunction, altered mental status, and head and face dyskinesias. The most common etiologies are idiopathic, paraneoplastic, and infectious encephalitis. Radiographic and pathological studies suggest brain-stem dysfunction with associated cerebellar and/or cerebellar pathway dysfunction. In many cases, there is evidence for the involvement of immunologic and/or inflammatory processes in the pathogenesis of this syndrome. The timely recognition of this syndrome is important because of its implications for the underlying etiology and prognosis. The appearance of this syndrome should prompt the search for an occult malignancy.
Insights
Adult opsoclonus-myoclonus syndrome can be a sign of systemic carcinoma. Early recognition is crucial for diagnosing occult malignancy and improving patient prognosis.
Area of Science:
- Neurology
- Oncology
Background:
- Opsoclonus-myoclonus syndrome (OMS) is a rare neurological disorder.
- It is characterized by involuntary, rapid eye movements (opsoclonus) and muscle jerks (myoclonus).
Observation:
- This study presents three adult cases of OMS associated with systemic carcinoma.
- Clinical manifestations included ataxia, tremor, gait disturbances, altered mental status, and dyskinesias.
Findings:
- Pathological and radiographic evidence points to brainstem dysfunction, often with cerebellar involvement.
- Immunologic and inflammatory processes are implicated in the syndrome's pathogenesis.
Implications:
- The presence of OMS in adults warrants a thorough search for an occult malignancy.
- Timely diagnosis is critical for determining underlying etiology and prognosis.
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