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...

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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 em: BMJ Publishing Group 2010
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Article
Acesso em linha: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
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