Kikuchi-Fujimoto Disease, a Rare Case of Lymphadenopaties

Authors

  • Rodolfo Gomes Serviço de Medicina Interna, Hospital Beatriz Ângelo, Loures, Portugal
  • Henrique Pina Serviço de Medicina Interna, Hospital Beatriz Ângelo, Loures, Portugal
  • Marta Ferreira Serviço de Medicina Interna, Hospital Beatriz Ângelo, Loures, Portugal
  • Maria Maia Serviço de Medicina Interna, Hospital Beatriz Ângelo, Loures, Portugal
  • Gonçalo Gerardo Serviço de Medicina Interna, Hospital Beatriz Ângelo, Loures, Portugal
  • Joana Filipa Oliveira Serviço de Medicina Interna, Hospital Beatriz Ângelo, Loures, Portugal
  • Fernando Martos Gonçalves Serviço de Medicina Interna, Hospital Beatriz Ângelo, Loures, Portugal

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https://doi.org/10.60591/crspmi.6

Keywords:

Histiocytic Necrotizing Lymphadenitis, Lymphadenopathy

Abstract

Kikuchi-Fujimoto disease, or histiocytic necrotizing lymphadenitis, is a rare disease, of unknown cause. It is characterized by cervical lymphadenopathies and fever, and has usually a benign course. Its diagnosis is based on histopathologic examination, and it is important to distinguish from infectious and lymphoproliferative disorders that are clinically similar but with completely different treatment and prognosis. Besides that, it is important to be aware of its association with autoimmune diseases, namely systemic lupus erythematosus.

 

We report a clinical case of a young woman with fever and right supraclavicular lymphadenopathies, admitted with the suspicion of a lymphoproliferative syndrome, whose biopsy revealed this condition.

References

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Published

2023-03-31

How to Cite

Gomes, R., Pina, H., Ferreira, M., Maia, M., Gerardo, G., Oliveira, J. F., & Martos Gonçalves, F. (2023). Kikuchi-Fujimoto Disease, a Rare Case of Lymphadenopaties. SPMI Case Reports, 1(1), 10–15. https://doi.org/10.60591/crspmi.6

Issue

Section

Casos Clínicos

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