Myasthenia gravis and mitochondrial myopathy may present with similar clinical symptoms as inconstant palpebral ptosis, ophthalmoparesis, and muscle weakness. A few case initially diagnosed as myasthenia gravis by a positive decremental response on EMG and successful anticholinesterase therapy revealed to be affected by mitochondrial disease. We report a new case initially found to be affected by myasthenia gravis in whom muscle biopsy, performed because of symptom worsening, disclosed a mitochondrial myopathy. It is not clear if the association of mitochondrial myopathy and myasthenia gravis is coincidental or if there is a pathogenic link between the two pathologies. We suggest that muscle biopsy should be performed in cases with atypical myasthenia gravis signs.
Plewnia, K., Dotti, M., Malandrini, A., Manneschi, L., Battisti, C., DE STEFANO, N., et al. (1997). A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case. JOURNAL OF SUBMICROSCOPIC CYTOLOGY AND PATHOLOGY, 29(3), 335-338.
A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case
DOTTI, MARIA;MALANDRINI, ALESSANDRO;BATTISTI, CARLA;DE STEFANO, NICOLA;RUFA, ALESSANDRA;MOTOLESE, EDUARDO;FEDERICO, ANTONIO
1997-01-01
Abstract
Myasthenia gravis and mitochondrial myopathy may present with similar clinical symptoms as inconstant palpebral ptosis, ophthalmoparesis, and muscle weakness. A few case initially diagnosed as myasthenia gravis by a positive decremental response on EMG and successful anticholinesterase therapy revealed to be affected by mitochondrial disease. We report a new case initially found to be affected by myasthenia gravis in whom muscle biopsy, performed because of symptom worsening, disclosed a mitochondrial myopathy. It is not clear if the association of mitochondrial myopathy and myasthenia gravis is coincidental or if there is a pathogenic link between the two pathologies. We suggest that muscle biopsy should be performed in cases with atypical myasthenia gravis signs.File | Dimensione | Formato | |
---|---|---|---|
26.pdf
non disponibili
Tipologia:
Post-print
Licenza:
NON PUBBLICO - Accesso privato/ristretto
Dimensione
1.6 MB
Formato
Adobe PDF
|
1.6 MB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
https://hdl.handle.net/11365/23327
Attenzione
Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo