Kikuchi-Fujimoto’s Disease And Systemic Lupus Erythematosus

Authors

  • Margarida Gonçalves Serviço de Medicina II – Hospital Central do Funchal
  • Gonçalo Silva Serviço de Medicina II – Hospital Central do Funchal
  • Augusto Barros Serviço de Medicina II – Hospital Central do Funchal
  • Luís Freitas Serviço de Medicina II – Hospital Central do Funchal
  • Paula Caldeira Serviço de Medicina II – Hospital Central do Funchal
  • Rita Rodrigues Serviço de Medicina II – Hospital Central do Funchal
  • Filipa Capelinha Serviço de Medicina II – Hospital Central do Funchal
  • Ema Freitas Serviço de Medicina II – Hospital Central do Funchal
  • Cláudia Fraga Serviço de Medicina II – Hospital Central do Funchal
  • José Camacho Serviço de Medicina II – Hospital Central do Funchal
  • António Caldeira Ferreira Serviço de Medicina II – Hospital Central do Funchal

Keywords:

Kikuchi and Fujimoto’s Disease, Histiocytic Necrotizing Lymphadenopathy, Systemic Lupus Erythematosus, Discoid Lupus Erythematosus

Abstract

Kikuchi and Fujimoto’s Disease, also known as Histiocytic Necrotizing Lymphadenopathy, is a rare and, usually, benign disorder,
of unknown aetiology. Generally presents with lymphadenopathy
and fever. Its association with systemic lupus erythematosus is
recognised and it can be diagnosed before, simultaneously or
after the diagnosis of lupus. The authors report a clinical case
of a female patient in whom Systemic Lupus Erythematosus
was diagnosed 10 years after Kikuchi and Fujimoto’s Disease in complete remission.

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References

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Additional Files

Published

2009-06-30

How to Cite

1.
Gonçalves M, Silva G, Barros A, Freitas L, Caldeira P, Rodrigues R, Capelinha F, Freitas E, Fraga C, Camacho J, Caldeira Ferreira A. Kikuchi-Fujimoto’s Disease And Systemic Lupus Erythematosus. RPMI [Internet]. 2009 Jun. 30 [cited 2024 Nov. 25];16(2):112-6. Available from: https://revista.spmi.pt/index.php/rpmi/article/view/1403

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Section

Case Reports

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