Review and Updates on Systemic Mastocytosis and Related Entities.
KIT
WHO 5th Edition Classification of Haematolymphoid Tumours (WHO 5th edition)
classification
diagnosis
hereditary alpha-tryptasemia (HαT or HAT)
mast cell activation syndrome (MCAS)
molecular
systemic mastocytosis (SM)
the International Consensus Classification (2022 ICC)
treatment
Journal
Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829
Informations de publication
Date de publication:
28 Nov 2023
28 Nov 2023
Historique:
received:
27
10
2023
revised:
16
11
2023
accepted:
24
11
2023
medline:
9
12
2023
pubmed:
9
12
2023
entrez:
9
12
2023
Statut:
epublish
Résumé
Mast cell disorders range from benign proliferations to systemic diseases that cause anaphylaxis and other diverse symptoms to mast cell neoplasms with varied clinical outcomes. Mastocytosis is the pathologic process of the accumulation of abnormal mast cells in different organs, mostly driven by
Identifiants
pubmed: 38067330
pii: cancers15235626
doi: 10.3390/cancers15235626
pmc: PMC10705510
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
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