A 76-year-old woman with a history of granulomatous pulmonary disease presented with myasthenia gravis involving ocular, pharyngeal, and proximal extremity weakness. She responded to prednisone therapy but three years later developed predominantly distal appendicular weakness. Reinvestigation demonstrated a granulomatous inflammatory myopathy.
|Original language||English (US)|
|Number of pages||3|
|Journal||Archives of Neurology|
|State||Published - Jun 1986|
ASJC Scopus subject areas
- Arts and Humanities (miscellaneous)
- Clinical Neurology