We describe a case of persistent microscopic hematuria as initial finding in incomplete Still's disease or Wissler-Fanconi syndrome. Renal biopsy findings were compatible with intravascular coagulation. Wissler-Fanconi syndrome and the associated renal abnormalities are briefly reviewed.
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Wissler-Fanconi syndrome and related diagnoses: a case report.
Open Access Rheumatol
June 2016
Division of Rheumatology, Utica Park Clinic, Tulsa, OK, USA.
Introduction: Wissler-Fanconi syndrome is a rare rheumatic syndrome that was first described during the 1940s in Europe. Since then, many papers have been written that cover all aspects of this syndrome, most of which are in French and German language, with only a very few in English (none of them recent). We report here a case that fulfils the criteria for Wissler-Fanconi syndrome.
View Article and Find Full Text PDFA 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.
View Article and Find Full Text PDF[Subsepsis allergica in a patient with type I polyglandular autoimmune syndrome].
Monatsschr Kinderheilkd
September 1990
Kinderklinik des St.-Marien- und St.-Annastifts-Krankenhauses, Ludwigshafen.
A 10.6 year old Turkish girl developed + the signs of a polyglandular autoimmune syndrome (PGA) type I since her first year of age. Apart from the endocrine and non-endocrine symptoms of PGA, she suffered from an acute state of illness with therapy-resistant fever and multiform exanthemas in the early course of disease.
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