Systemic Mastocytosis Associated with Chronic Idiopathic Myelofibrosis: A Distinct Subtype of Systemic Mastocytosis-Associated Clonal Hematological Nonmast Cell Lineage Disorder Carrying the Activating Point Mutations KIT(D816V) and JAK2(V617F)

In ∼20 to 30% of patients with systemic mastocytosis (SM), an associated clonal hematological nonmast cell lineage disorder (AHNMD) is diagnosed. Although SM may be considered to be closely related to the myeloproliferative disorders (MPDs), it is unknown whether JAK2(V617F+) MPD may occur as AHNMD...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Autori principali: Sotlar, Karl, Bache, Anja, Stellmacher, Florian, Bültmann, Burkhard, Valent, Peter, Horny, Hans-Peter
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Society for Investigative Pathology 2008
Soggetti:
Regular Articles
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2175544/
https://ncbi.nlm.nih.gov/pubmed/18165278
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/jmoldx.2008.070061
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi