RESUMEN
INTRODUCCIÓN: El dermatofibroma es uno de los tumores cutáneos benignos más frecuentes. Suele aparecer en las extremidades inferiores entre la tercera y la quinta década de la vida, siendo más frecuente en mujeres. El diagnóstico clínico frecuentemente es sencillo. Se asocia a una tasa muy baja de recidivas locales tras la extirpación. OBJETIVOS: Presentar nuestra experiencia en dermatofibromas de localización facial con el fin de discutir las características clínicas e histopatológicas en esta localización. MATERIAL Y MÉTODOS: Estudio retrospectivo descriptivo de las características clínico-patológicas de los dermatofibromas de localización facial diagnosticados en el Departamento de Dermatología del Hospital General Universitario de Valencia entre los años 1990 y 2012. RESULTADOS: Se incluyeron 20 casos de dermatofibromas de localización facial (1,11% de los diagnosticados en todas las localizaciones). Estas lesiones mostraron un amplio rango de edad de aparición, que osciló de 28 a 84 años, con una media de 57,15 años y una mediana de 54 años. La distribución por sexo fue de 11 mujeres y 9 hombres. El promedio de seguimiento fue de 83 meses, con ninguna recurrencia local. Todos los casos estaban confinados en la dermis papilar y reticular, y el patrón de crecimiento predominante fue el estoriforme. CONCLUSIONES: El estudio de los dermatofibromas de localización facial observados en nuestro centro en un período de 22 años sugiere que esta es una localización infrecuente, pero que en la mayoría de los casos tiene un comportamiento similar al de otras localizaciones
INTRODUCTION: Dermatofibroma is one of the most common benign skin tumors. It typically develops on the lower limbs between the third and fifth decade of life and is more common in women. Clinical diagnosis is often straightforward. Dermatofibromas are associated with a very low rate of local recurrence following excision. OBJECTIVES: To describe the clinical and histologic features of dermatofibroma of the face based on our experience. MATERIALS AND METHODS: Descriptive retrospective study of the clinicopathologic features of dermatofibromas of the face diagnosed at the dermatology department of Hospital General Universitario de Valencia between 1990 and 2012. RESULTS: Twenty cases of dermatofibroma of the face (1.11% of all dermatofibromas diagnosed) were studied. The age at onset varied widely, from 28 to 84 years. The mean age at onset was 57.15 years and the median was 54 years. There were 11 women and 9 men. Mean follow-up was 83 months and there were no local recurrences. All the tumors were confined to the papillary and reticular dermis and the storiform pattern was the most common growth pattern observed. CONCLUSIONS: This study of facial dermatofibromas diagnosed at our hospital over a period of 22 years suggests that the face is an uncommon site but that dermatofibromas in this location behave similarly to those occurring elsewhere on the body
Asunto(s)
Humanos , Histiocitoma Fibroso Benigno/diagnóstico , Neoplasias Faciales/diagnóstico , Tejido Conectivo/patología , Estudios Retrospectivos , Distribución por Edad y SexoRESUMEN
INTRODUCTION: Dermatofibroma is one of the most common benign skin tumors. It typically develops on the lower limbs between the third and fifth decade of life and is more common in women. Clinical diagnosis is often straightforward. Dermatofibromas are associated with a very low rate of local recurrence following excision. OBJECTIVES: To describe the clinical and histologic features of dermatofibroma of the face based on our experience. MATERIALS AND METHODS: Descriptive retrospective study of the clinicopathologic features of dermatofibromas of the face diagnosed at the dermatology department of Hospital General Universitario de Valencia between 1990 and 2012. RESULTS: Twenty cases of dermatofibroma of the face (1.11% of all dermatofibromas diagnosed) were studied. The age at onset varied widely, from 28 to 84 years. The mean age at onset was 57.15 years and the median was 54 years. There were 11 women and 9 men. Mean follow-up was 83 months and there were no local recurrences. All the tumors were confined to the papillary and reticular dermis and the storiform pattern was the most common growth pattern observed. CONCLUSIONS: This study of facial dermatofibromas diagnosed at our hospital over a period of 22 years suggests that the face is an uncommon site but that dermatofibromas in this location behave similarly to those occurring elsewhere on the body.
Asunto(s)
Neoplasias Faciales/patología , Histiocitoma Fibroso Benigno/patología , Neoplasias Cutáneas/patología , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios RetrospectivosRESUMEN
Overexpression of epidermal growth factor receptor (EGFR) is associated with enhanced activation of wild-type (hyperactive) Ras in breast cancer. Little is known about the regulation of Ras inactivation and GTPase-activating proteins (GAPs), such as p120GAP, in cells with hyperactive Ras. Recently, we showed that in EGFR-overexpressing A431 cells, which lack endogenous Annexin A6 (AnxA6), ectopic expression of AnxA6 stimulates membrane recruitment of p120GAP to modulate Ras signalling. We now demonstrate that, AnxA6 is downregulated in a number of EGFR-overexpressing and estrogen receptor (ER)-negative breast cancer cells. In these cells, AnxA6 overexpression promotes Ca(2+)- and EGF-inducible membrane targeting of p120GAP. In ER-negative MDA-MB-436 cells, overexpression of p120GAP, but not CAPRI or a p120GAP mutant lacking the AnxA6-binding domain inhibits Ras/MAPK activity. AnxA6 knockdown in MDA-MB-436 increases Ras activity and cell proliferation in anchorage-independent growth assays. Furthermore, AnxA6 co-immunoprecipitates with H-Ras in a Ca(2+)- and EGF-inducible manner and fluorescence resonance energy transfer (FRET) microscopy confirmed that AnxA6 is in close proximity of active (G12V), but not inactive (S17N) H-Ras. Thus, association of AnxA6 with H-Ras-containing protein complexes may contribute to regulate p120GAP/Ras assembly in EGFR-overexpressing and ER-negative breast cancer cells.
Asunto(s)
Anexina A6/metabolismo , Proteínas Proto-Oncogénicas p21(ras)/metabolismo , Transducción de Señal , Proteína Activadora de GTPasa p120/metabolismo , Animales , Anexina A6/antagonistas & inhibidores , Calcio/metabolismo , Membrana Celular/metabolismo , Proliferación Celular , Cricetinae , Cricetulus , Ciclina D1 , Receptores ErbB/metabolismo , Transferencia Resonante de Energía de Fluorescencia , Técnica del Anticuerpo Fluorescente , Humanos , Inmunoprecipitación , Proteínas Proto-Oncogénicas p21(ras)/genética , ARN Interferente Pequeño/farmacología , Receptores de Estrógenos/metabolismo , Células Tumorales Cultivadas/efectos de los fármacos , Células Tumorales Cultivadas/metabolismo , Proteína Activadora de GTPasa p120/genéticaRESUMEN
Two anti-inflammatory principles were isolated from the methanol extract of the leaves of Erythrospermum monticolum (Flacourtiaceae). The isolation was based on a guided bioassay of the inhibitory activity on TPA-induced ear edema in mice. These compounds were identified as quercetin 3-O-xylosyl(1-->2) rhamnoside and quercetin 3-O-rhamnoside. In addition, their effects on a chronic topic inflammation model were evaluated.