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

Campos Domínguez M, Suárez Fernández R. Enfermedad de Kimura e hiperplasia angiolinfoide con eosinofilia. ¿La misma enfermedad o distintas entidades? Piel (Barc) 2017; 33: 279-281. Accesible en: https://www.sciencedirect.com/science/article/pii/S0213925117303659 (último acceso oct. 2022). DOI: https://doi.org/10.1016/j.piel.2017.08.013

Ailing Zou A, Hu M, Niu B. Comparison between Kimura’s disease and angiolymphoid hyperplasia with eosinophilia: case reports and literature review. J Int Med Res. 2021; 49 (9): 1-8. Accesible en https://doi.org/10.1177/03000605211040976 (último acceso oct. 2022). DOI: https://doi.org/10.1177/03000605211040976

Kung IT, Gibson JB, Bannatyne PM. Kimura's disease: a clinico-pathological study of 21 cases and its distinction from angiolymphoid hyperplasia with eosinophilia. Pathology. 1984; 16(1): 39-44. Accesible en: https://dx.doi.org/10.3109/00313028409067909 (último acceso oct. 2022). DOI: https://doi.org/10.3109/00313028409067909

Kuo TT, Shih LY, Chan HL. Kimura's disease. Involvement of regional lymph nodes and distinction from angiolymphoid hyperplasia with eosinophilia. Am J Surg Pathol. 1988; 12(11): 843-854. DOI: https://doi.org/10.1097/00000478-198811000-00005

Park SW, Kim HJ, Sung KJ, et al. Kimura disease: CT and MR imaging findings. AJNR Am J Neuroradiol 2012; 33(4): 784-788. Accesible en: https://dx.doi.org/10.3174/ajnr.A2854 (último acceso oct. 2022). DOI: https://doi.org/10.3174/ajnr.A2854

Kottler D, Barète S, Quéreux G, Ingen-Housz-Oro S, Fraitag S, Ortonne N et al. Retrospective multicentric study of 25 Kimura disease patients: emphasis on therapeutics and shared features with cutaneous IgG4-related disease. Dermatology 2015; 231(4): 367-377. Accesible en: https://doi.org/10.1159/000439346 (último acceso oct. 2022). DOI: https://doi.org/10.1159/000439346

Ye P, Wei T, Yu GY, Wu LL, Peng X. Comparison of local recurrence rate of three treatment modalities for Kimura disease. J Craniofac Surg 2016; 27(1): 170-174. Accesible en: https://doi.org/10.1097/SCS.0000000000002337 (último acceso oct. 2022). DOI: https://doi.org/10.1097/SCS.0000000000002337

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 Jul. 3];7(3):17-20. Available from: https://www.reccmi.com/RECCMI/article/view/791

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