Zusammenfassung
Der adulte Morbus Still ist eine seltene entzündliche
Systemerkrankung. Leitsymptome/-manifestationen sind
Fieber, Arthralgien oder Arthritis, Myalgien, ein typischer Hautausschlag,
Halsschmerzen, Hepatosplenomegalie, Lymphadenopathie und Serositis.
Zahlreiche weitere Symptome und Organmanifestationen sind jedoch
möglich. Das klinische Erscheinungsbild ist variabel und
kann leicht bis lebensbedrohlich ausgeprägt sein. Der Erkrankungsverlauf
ist spontan-limitierend, intermittierend oder chronisch. Da ein
beweisendes diagnostisches Testverfahren nicht vorhanden ist, kann
die Diagnose erst nach Ausschluss zahlreicher, vor allem infektiöser,
maligner und autoimmuner Differentialdiagnosen gestellt werden.
Zur Therapie können nichtsteroidale Antiphlogistika, Glucocorticoide,
Basistherapeutika und Biologika eingesetzt werden.
Abstract
Adult-onset Still’s disease is a rare inflammatory systemic
disease. Cardinal symptoms/manifestations are fever,
arthralgias or arthritis, myalgias, the typical skin rash, sore
throat, hepatosplenomegaly, lymphadenopathy and serositis. Several
other symptoms and organ involvements are possible. The clinical
picture is variable with mild to life-threatening courses. The disease
is self-limiting, intermittently active or chronic. Because of the
lack of a defined diagnostic test the diagnosis of AOSD can only
be made after exclusion of several differential diagnoses in particular
of infectious, malignant and autoimmune origin. For therapy non-steroidal
anti-inflammatory drugs, glucocorticoids, disease modifying antirheumatic
drugs and biologics can be used.
Schlüsselwörter
adulter Morbus Still - Morbus Still des Erwachsenen - adult-onset Still’s disease (AOSD)
Keywords
Still’s disease - adult-onset Still’s disease - AOSD
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Dr. med. Claudia Dechant
Rheumaeinheit, Medizinische Poliklinik
Klinikum
der Universität
München – Campus
Innenstadt
Pettenkoferstr. 8a
80336 München
Email: claudia.dechant@med.uni-muenchen.de