Dilemas de diagnóstico de linfadenite necrotizante (doença de Kikuchi-Fujimoto).

Autores

  • Inês Antunes Serviço de Medicina Interna, Hospital São Francisco Xavier (CHLO), Lisbon, Portugal.
  • Arturo Botella
  • Filipa Marques
  • Inês Araújo
  • Ana Abreu
  • Rosa Cardiga
  • Ana Leitão
  • Cândida Fonseca
  • Fátima Ceia

DOI:

https://doi.org/10.20344/amp.1540

Resumo

Kikuchi-Fujimoto disease, also called Histiocytic necrotizing lymphadentis, is a rare, benign and self-limited disease, with unknown etiology, that affects mainly young women, and is characterized by adenopathy (usually localized in the cervical region) and fever. Diagnosis is based on histopathological findings in ganglionar tissue obtained in excisional biopsy, which allows, in most cases, the differential diagnosis with other similar clinical conditions, but which have a completely different clinical evolution and therapeutic needs. We report a case of a twenty four year old woman with persistent cervical lymphadenopathy, in which histopathological examination followed by immunohistochemical analysis of ganglionar tissue revealed to be Kikuchi-Fujimoto disease.

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1.
Antunes I, Botella A, Marques F, Araújo I, Abreu A, Cardiga R, Leitão A, Fonseca C, Ceia F. Dilemas de diagnóstico de linfadenite necrotizante (doença de Kikuchi-Fujimoto). Acta Med Port [Internet]. 30 de Dezembro de 2011 [citado 17 de Julho de 2024];24:681-4. Disponível em: https://actamedicaportuguesa.com/revista/index.php/amp/article/view/1540

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