Literature DB >> 18700190

Granulomatous myositis mimicking slowly progressive lower motor neuron disease.

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.

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Year:  2008        PMID: 18700190

Source DB:  PubMed          Journal:  Eur J Med Res        ISSN: 0949-2321            Impact factor:   2.175


  1 in total

1.  LETTER TO THE EDITOR Atypical Granulomatous Myositis and Pulmonary Sarcoidosis.

Authors:  Renata Siciliani Scalco; Stefen Brady; Jefferson Becker; Irenio Gomes; Janice L Holton; Henrique L Staub
Journal:  Open Rheumatol J       Date:  2015-07-10
  1 in total

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