Haemophagocytic syndrome and Still’s Disease in the Adult

Authors

  • Filipa Aragão Carvalho Interna do Internato Complementar de Medicina Interna, Serviço de Medicina II do Hospital Fernando Fonseca, Amadora
  • Alice Rodrigues Assistente Hospitalar de Medicina Interna, Serviço de Medicina II do Hospital Fernando Fonseca, Amadora
  • Carmen Andujar Assistente Hospitalar de Medicina Interna, Serviço de Medicina II do Hospital Fernando Fonseca, Amadora
  • Luís Dutschmann Director do Serviço de Medicina II do Hospital Fernando Fonseca, Amadora

Keywords:

Adult Still´s disease, hyperferritinaemia, haemophagocytic syndrome

Abstract

Adult Still’s disease is a rare disease found worlwide. It presents
as an acute febrile syndrome that affects multiple organs. Although
the diagnosis is one of exclusion, a striking constellation of clinical
and laboratory abnormalities is present.
The authors report a case of Adult Still´s Disease in a 58-year- s Disease in a 58-year old woman who presented with fever, arthralgia, sore throat, rash and myalgia and elevated serum ferritin. Although the patient
initially responded favourably to corticotherapy, the outcome was
fatal. The authors discuss the macrophage activation syndrome
as a complication of chronic rheumatic diseases and as a consequence of Parvovirus infection.

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References

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Additional Files

Published

2004-06-30

How to Cite

1.
Aragão Carvalho F, Rodrigues A, Andujar C, Dutschmann L. Haemophagocytic syndrome and Still’s Disease in the Adult. RPMI [Internet]. 2004 Jun. 30 [cited 2024 Dec. 18];12(2):77-81. Available from: https://revista.spmi.pt/index.php/rpmi/article/view/1682

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