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Primary systemic amyloidosis presenting with polyneuropathy characterized by very long survival
R Rinaldi1, G Azzimondi, P Preda
1Neurology Unit, S. Orsola-Malpighi Hospital, Bologna, Italy.
Acta Neurologica Scandinavica
|June 1, 1995
Abstract:
We report a case of primary systemic amyloidosis associated with IgA monoclonal gammopathy presenting with sensorimotor polyneuropathy. For 10 years the neurological symptoms were the only clinical manifestation. A great deal of therapy was given right from the onset of symptoms and the very long survival of the patient may have been due to these efforts.