Artículos de revistas
Bazex Syndrome (acrokeratosis Paraneoplastica) Diagnosed In A Patient With Oral Persistent Ulcerations.
Registro en:
Head And Neck Pathology. v. 4, n. 4, p. 312-7, 2010-Dec.
1936-0568
10.1007/s12105-010-0203-5
20721648
Autor
Santos-Silva, Alan Roger
Correa, Marcelo Brum
Vargas, Pablo Agustin
Almeida, Oslei Paes
Lopes, Marcio Ajudarte
Institución
Resumen
Paraneoplastic syndromes associated with head and neck cancer are rare and have been reported under dermatological, endocrine, hematological, neurological and rheumatological disorders. Bazex syndrome is an intriguing paraneoplasia that can be associated with head and neck squamous cell carcinomas. A range of symmetrical dermatological manifestations, with a clear predilection to extremities, that encompasses erythematous squamous plaques, skin scaling and nail dystrophy can provide a psoriasiform pattern in Bazex syndrome. In addition to these tricky clinical features, the rarity of the disease and the lack of understanding on Bazex syndrome generally make such cases to be mismanaged as psoriasis or lichen planus, causing an important delay in the diagnosis of the underlying malignancy. The authors describe a case of Bazex syndrome that occurred in a patient with a recently diagnosed tongue squamous cell carcinoma. Clinicians should consider paraneoplasia when assessing skin and/or oral persistent lesions. 4 312-7