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Gewählte Publikation:

Fink-Puches, R; Smolle, J; Kerl, H.
Wissler's allergic subsepsis
HAUTARZT. 1994; 45(2): 80-83. Doi: 10.1007%2Fs001050050042 (- Case Report)
Web of Science PubMed FullText FullText_MUG

 

Führende Autor*innen der Med Uni Graz
Fink-Puches Regina
Co-Autor*innen der Med Uni Graz
Kerl Helmut
Smolle Josef
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Abstract:
A 20-year-old female patient with the typical signs of Wissler's subsepsis allergica (Wissler-Fanconi syndrome) is described. This rare disease is characterized by four typical symptoms: polymorphous exanthemas, recurrent high fever, leucocytosis and arthralgia. In the early stages it is difficult to differentiate from septicaemia. This syndrome has sometimes been considered equivalent to or an initial stage of Still's disease (juvenile rheumatoid arthritis) progressing to degenerative arthritis in many patients, whereas other authors have classified it as a separate entity with good prognosis. The present case demonstrates that Wissler's subsepsis allergica should be considered when ever transient polymorphous exanthema is accompanied by high recurrent fever, leucocytosis and arthralgia.
Find related publications in this database (using NLM MeSH Indexing)
Adult -
Biopsy -
Diagnosis, Differential -
Dose-Response Relationship, Drug -
Female -
Humans -
Leukocyte Count - drug effects
Long-Term Care - drug effects
Methylprednisolone - administration and dosage
Prednisolone - administration and dosage
Skin - pathology
Wissler's Syndrome - diagnosis

Find related publications in this database (Keywords)
Subsepsis-Allergica Wissler
Polymorphous Exanthema
Recurrent High Fever
Leukocytosis
Arthralgia
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