CareLit Fachartikel

Inflammatory Myopathies

D Pongratz · Klinische Neurophysiologie · 2004 · Heft 08

Dokument
1101298
CareLit-ID
Jahr
2004
Publikation
PDF
nein
Metadaten
DOI
ja
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Bibliografische Angaben

Zeitschrift
Klinische Neurophysiologie
Autor:innen
D Pongratz
Ausgabe
Heft 08 / 2004
Seiten
–
Erschienen: 2004-08-25 00:00:00
ISSN
1434-0275

Zusammenfassung

Inflammatory myopathies represent a small but important group of acquired muscular disorders. The most important forms of immunogenic inflammatory myopathies are dermatomyositis (DM), polymyositis (PM) and inclusion body myositis (IBM). A hallmark of all types of immunogenic inflammatory myopathies is infiltration (B-cells, CD4+ and CD8+ T cells and macrophages) in muscle tissue. In DM, inflammatory infiltrates with B-cells and CD4+ T cells are found predominantly in perivascular and perifascicular regions, producing the picture of a myositis of the perifascicular type. There are striking lesions of the small in…

Schlagworte

Klinische Neurophysiologie