Systemic mastocytosis with KIT V560G mutation presenting as recurrent episodes of vascular collapse: response to disodium cromoglycate and disease outcome

BACKGROUND: Mastocytosis are rare diseases characterized by an accumulation of clonal mast cells (MCs) in one or multiple organs or tissues. Patients with systemic mastocytosis (SM), whose MCs frequently arbor the activating D816V KIT mutation, may have indolent to aggressive diseases, and they may...

Descripción completa

Detalles Bibliográficos
Autores principales: Conde-Fernandes, Iolanda, Sampaio, Rita, Moreno, Filipa, Palla-Garcia, José, Teixeira, Maria dos Anjos, Freitas, Inês, Neves, Esmeralda, Jara-Acevedo, Maria, Escribano, Luis, Lima, Margarida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402055/
https://www.ncbi.nlm.nih.gov/pubmed/28439288
http://dx.doi.org/10.1186/s13223-017-0193-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402055/
https://www.ncbi.nlm.nih.gov/pubmed/28439288
http://dx.doi.org/10.1186/s13223-017-0193-x

Ejemplares similares