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International Journal of Medicine Sciences

Vol. 1, Issue 1, Part A (2019)

Atypical chronic rhinosinusitis in Papillon syndrome -Lefevre: Presentation of 2 cases

Author(s):

Juan Antonio Lugo, Ruth Salazar, Nadia Zavala, Oscar Rodríguez, Gerardo Vargas, Lorenzo Lizárraga, Alejandra Pineda, Irene Arellano, Pablo Luna, Fernanda Barragán, Mario Sepúlveda

Abstract:
Papillon-Lefebre syndrome (SPL) is an extremely rare autosomal recessive disorder characterized by palmoplantar keratoderma and periodontitis, with an estimated incidence of 1-4 cases per million. Patients with SPL are highly susceptible to infection. The etiology of this susceptibility is unknown; however, an association with defects in neurophilic dysfunction, insufficient response of lymphocytes, defects in monocyte functions and deterioration of cytotoxic function of NK cells has been suggested. The manifestations include oral cavity specifically at the dental level, however at the level of paranasal sinuses there is a singular manifestation little known, as our two cases. We propose the criteria of Lugo cols. for diagnosis

Pages: 19-21  |  1692 Views  656 Downloads


International Journal of Medicine Sciences
How to cite this article:
Juan Antonio Lugo, Ruth Salazar, Nadia Zavala, Oscar Rodríguez, Gerardo Vargas, Lorenzo Lizárraga, Alejandra Pineda, Irene Arellano, Pablo Luna, Fernanda Barragán, Mario Sepúlveda. Atypical chronic rhinosinusitis in Papillon syndrome -Lefevre: Presentation of 2 cases. Int. J. Med. Sci. 2019;1(1):19-21. DOI: 10.33545/26648881.2019.v1.i1a.5