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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Auteurs principaux: Rossi, Elisa, Boeri, Laura, Morbini, Patrizia, Pagella, Fabio, Colombo, Andrea, Matti, Elina, Olivieri, Carla, Villanacci, Vincenzo, Minelli, Antonella, Buscarini, Elisabetta, Canzonieri, Cecilia, Danesino, Cesare
Format: Artigo
Langue:Inglês
Publié: BMJ Publishing Group 2010
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Article
Accès en ligne: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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