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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...

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Detalhes bibliográficos
Publicado no:Allergy Asthma Clin Immunol
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2017
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5402055/
https://ncbi.nlm.nih.gov/pubmed/28439288
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13223-017-0193-x
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