Acroqueratosis de Bazex: Two case reports

Authors

  • Liliana Filipa Invêncio da Costa Serviço de Otorrinolaringologia - Complexo Hospitalario Universitario A Coruña.
  • Fabian Alzate Amaya Serviço de Otorrinolaringologia - Complexo Hospitalario Universitario A Coruña.
  • Anselmo Padin Seara Serviço de Otorrinolaringologia - Complexo Hospitalario Universitario A Coruña.
  • Jaime Villares Soriano Serviço de Otorrinolaringologia - Complexo Hospitalario Universitario A Coruña.

DOI:

https://doi.org/10.34631/sporl.705

Keywords:

Síndrome de Bazex, Acroqueratose, Síndrome paraneoplásico, carcinoma epidermoide, orofaringe

Abstract

The Bazex syndrome is a very infrequent paraneoplastic dermatosis, characterized by the appearance of psoriasiform acral hyperkeratosis that is mainly related to epidermoid carcinomas of upper aero-digestive tract. Between 60-70%(1) of the diagnosis precedes the associated tumor. We describe two clinical cases representing the typical characteristics of this pathology in order to explain and highlight the importance of its early recognition, which facilitates rapid identification of the tumor, thus increasing survival.

References

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Published

2018-08-21

How to Cite

da Costa, L. F. I., Alzate Amaya, F., Padin Seara, A., & Villares Soriano, J. (2018). Acroqueratosis de Bazex: Two case reports. Portuguese Journal of Otorhinolaryngology and Head and Neck Surgery, 56(1), 31–34. https://doi.org/10.34631/sporl.705

Issue

Section

Case Report