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1.
Int J Dermatol ; 57(12): 1447-1453, 2018 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-30168850

RESUMEN

BACKGROUND: The incidence of basal cell carcinoma (BCC) in younger individuals has increased in recent decades. However, the characteristics of BCCs in this population, especially in Ibero-Latin American countries, have not been completely defined. OBJECTIVE: To describe the demographic, clinical, and histopathological characteristics of BCCs in patients younger than 40 treated with Mohs Micrographic Surgery (MMS). MATERIALS AND METHODS: A multicenter, retrospective study conducted between January 2009 and December 2014, in five Ibero-American countries, included biopsy-proven BCCs in patients younger than 40 that were treated with MMS. Demographic, clinical, histopathological, and surgical characteristics were described. RESULTS: The study included 301 tumors in 241 patients, of whom 61% were female. The most common Fitzpatrick phototype was III. The most common histological subtypes were nodular (37.5%) and infiltrative (18.9%). Perineural invasion was encountered in 1.7%, and tumor clearance was achieved in 87.4% within two stages of MMS. CONCLUSIONS: This is the first Ibero-Latin American transnational study describing the characteristics of BCCs in young patients treated with MMS. Despite darker skin phototypes in this population, BCCs can occur in early ages and may present with aggressive features. Therefore, MMS may be considered an appropriate first-line treatment option in this population.


Asunto(s)
Carcinoma Basocelular/cirugía , Neoplasias Faciales/cirugía , Cirugía de Mohs , Recurrencia Local de Neoplasia , Neoplasias Cutáneas/cirugía , Adolescente , Adulto , Argentina , Brasil , Carcinoma Basocelular/patología , Carcinoma Basocelular/terapia , Niño , Preescolar , Colombia , Neoplasias Faciales/patología , Neoplasias Faciales/terapia , Femenino , Humanos , Lactante , Recién Nacido , Masculino , México , Invasividad Neoplásica , Recurrencia Local de Neoplasia/patología , Estudios Retrospectivos , Neoplasias Cutáneas/patología , Neoplasias Cutáneas/terapia , Pigmentación de la Piel , España , Adulto Joven
2.
Expert Rev Anticancer Ther ; 14(6): 741-9, 2014 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-24611655

RESUMEN

The hedgehog (Hh) signaling pathway has been identified as important to normal embryonic development in living organisms and it is implicated in processes including cell proliferation, differentiation and tissue patterning. Aberrant Hh pathway has been involved in the pathogenesis and chemotherapy resistance of different solid and hematologic malignancies. Basal cell carcinoma (BCC) and medulloblastoma are two well-recognized cancers with mutations in components of the Hh pathway. Vismodegib has recently approved as the first inhibitor of one of the components of the Hh pathway (smoothened). This review attempts to provide current data on the molecular pathways involved in the development of BCC and the therapeutic options available for the treatment of locally advanced and metastatic BCC, and the new targeted therapies in development.


Asunto(s)
Antineoplásicos/uso terapéutico , Carcinoma Basocelular/patología , Proteínas Hedgehog/antagonistas & inhibidores , Terapia Molecular Dirigida , Proteínas de Neoplasias/antagonistas & inhibidores , Transducción de Señal/efectos de los fármacos , Neoplasias Cutáneas/patología , Anilidas/farmacología , Anilidas/uso terapéutico , Antineoplásicos/farmacología , Carcinoma Basocelular/tratamiento farmacológico , Carcinoma Basocelular/etiología , Carcinoma Basocelular/radioterapia , Carcinoma Basocelular/secundario , Carcinoma Basocelular/cirugía , Resistencia a Antineoplásicos , Receptores ErbB/antagonistas & inhibidores , Proteínas Hedgehog/fisiología , Humanos , Proteínas de Neoplasias/fisiología , Neoplasias Inducidas por Radiación/tratamiento farmacológico , Neoplasias Inducidas por Radiación/patología , Neoplasias Inducidas por Radiación/cirugía , Células Madre Neoplásicas/efectos de los fármacos , Células Madre Neoplásicas/enzimología , Síndromes Neoplásicos Hereditarios/tratamiento farmacológico , Síndromes Neoplásicos Hereditarios/patología , Síndromes Neoplásicos Hereditarios/cirugía , Piridinas/farmacología , Piridinas/uso terapéutico , Receptores Acoplados a Proteínas G/antagonistas & inhibidores , Neoplasias Cutáneas/tratamiento farmacológico , Neoplasias Cutáneas/etiología , Neoplasias Cutáneas/radioterapia , Neoplasias Cutáneas/cirugía , Receptor Smoothened , Luz Solar/efectos adversos
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