From Surf Wiki (app.surf) — the open knowledge base
Wissler's syndrome
| Field | Value |
|---|---|
| name | Wissler's syndrome |
| synonyms | Wissler's disease or Wissler-Fanconi syndrome |
| Wissler's syndrome is a rheumatic disease that has a similar presentation to sepsis. It is sometimes considered closely related to Still's disease. It is named for Guido Fanconi and Hans Wissler. It was first described by Wissler in 1944 and Fanconi in 1946. Single observations by E. Uhse in 1943 («Febris maculosa intermittens»), Fykow in 1929 and Nowak in 1942.
Signs and symptoms
Presentation includes a symptom complex characterised by the clinical features of a high intermittent fever of septic type, constantly recurring exanthema, transient arthralgia, carditis, pleurisy, neutrophil leukocytosis, and increased erythrocyte sedimentation rate.
Causes
The etiology of the disease is uncertain. Wissler suggested an allergic reaction to bacteraemia as the pathogenic factor.
Epidemiology
Children and adolescents are most frequently affected; age in the reported cases varied from 5 to 17 years.
References
References
- (February 1994). "[Wissler's allergic subsepsis]". Hautarzt.
- {{WhoNamedIt. synd. 84
- H. Wissler. Über eine besondere Form sepsisähnlicher Krankheiten (Subsepsis hyperergica). Monatsschrift Kinderheilkunde, Berlin, 1943, 94: 1-15.
This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.
Ask Mako anything about Wissler's syndrome — get instant answers, deeper analysis, and related topics.
Research with MakoFree with your Surf account
Create a free account to save articles, ask Mako questions, and organize your research.
Sign up freeThis content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.
Report