Immunohistochemical analysis of a merkeloma observed in a patient affected by hereditary haemorrhagic telangiectasia

Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder characterised by epistaxis, telangiectases, and multiorgan vascular dysplasia. Mutations of the ENG and ACVRL1 genes cause at least 80% of cases. We report the first case of merkeloma found in a patient with HHT carrying...

Descrición completa

Gardado en:
Detalles Bibliográficos
Main Authors: Rossi, Elisa, Boeri, Laura, Morbini, Patrizia, Pagella, Fabio, Colombo, Andrea, Matti, Elina, Olivieri, Carla, Villanacci, Vincenzo, Minelli, Antonella, Buscarini, Elisabetta, Canzonieri, Cecilia, Danesino, Cesare
Formato: Artigo
Idioma:Inglês
Publicado: BMJ Publishing Group 2010
Assuntos:
Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3028296/
https://ncbi.nlm.nih.gov/pubmed/22315638
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr.09.2009.2251
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares