Atypical case of Kimura's disease in a 66-year-old man

Authors

  • Marina Campayo-Peña Internal Medicine Department, Hospital General de Albacete, Albacete, Spain
  • Amparo Puerta-García Internal Medicine Department, Hospital Quironsalud Albacete, Albacete, Spain
  • Carlota Rodríguez de Vera-Guardiola Anatomical Pathology Service, Hospital General de Albacete, Albacete, Spain
  • Mónica Campos-Pérez Radiodiagnostic Service, Hospital General de Albacete, Albacete, Spain
  • Manuel Vives-Soto Internal Medicine Department, Hospital Quironsalud Albacete, Albacete, Spain

DOI:

https://doi.org/10.32818/reccmi.a7n3a6

Keywords:

Kimura disease, angiolymphoid hyperplasia with eosinophilia, lymphadenopathy, eosinophilia, biopsy

Abstract

Kimura disease should be suspected when there are lymphoid masses or nodules in the head and neck, with subcutaneous cellular tissue involvement and regional lymphadenopathy, with minor inflammation and few systemic symptoms. It is usually associated with blood eosinophilia and elevated serum IgE. Even without treatment, it has a good prognosis, although recurrence is common. We present the case of a 66-year-old Caucasian male with a rapidly appearing laterocervical mass whose final diagnosis was made by biopsy. Biopsy showed mixed findings of Kimura disease and angiolymphoid hyperplasia with eosinophilia (ALHE), once thought to be the same disorder.

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References

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Published

2022-12-28

How to Cite

1.
Campayo-Peña M, Puerta-García A, Rodríguez de Vera-Guardiola C, Campos-Pérez M, Vives-Soto M. Atypical case of Kimura’s disease in a 66-year-old man. Rev Esp Casos Clin Med Intern [Internet]. 2022 Dec. 28 [cited 2024 Nov. 23];7(3):17-20. Available from: https://www.reccmi.com/RECCMI/article/view/791

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