| Literature DB >> 18700190 |
Hans-Jürgen Gdynia1, N Osterfeld, J Dorst, A C Ludolph, C A von Arnim, A-D Sperfeld.
Abstract
Here we illustrate a 74-year-old patient presenting with clinical signs of slowly progressive motor neuron disease. After electromyography demonstrated myopathic changes, a skeletal muscle biopsy was performed showing histological signs of granulomatous myositis. In extensive diagnostic workup underlying primary granulomas forming diseases were excluded and corticoid therapy was initiated, but without clinical effect. We want to point out that granulomatous myositis should be considered in the differential diagnosis of slowly progressive motor neuron diseases, especially in atypical clinical presentations.Entities:
Mesh:
Year: 2008 PMID: 18700190
Source DB: PubMed Journal: Eur J Med Res ISSN: 0949-2321 Impact factor: 2.175