| Literature DB >> 24745676 |
Hans-Peter Horny1, Karl Sotlar2, Peter Valent3.
Abstract
Mastocytosis is a disease of bone marrow origin histologically characterized by compact tissue infiltrates of atypical mast cells never seen in reactive states. Most patients with mastocytosis have transformed mast cells carrying an activating point mutation at codon 816 of KIT and also show an elevated serum tryptase level. In this article immunophenotypical features of mast cells are described. Based on these features, mast cells are not closely related to other myeloid cells. Using the knowledge on aberrantly expressed antigens by mast cells, the hematopathologist should be able to recognize the disease even in the presence of unusual morphologic findings or an associated hematologic non-mast cell lineage disease.Entities:
Keywords: CD117; CD30; Immunophenotype; Mast cell; Mast cell leukemia; Mastocytosis; Systemic mastocytosis; Tryptase
Mesh:
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Year: 2014 PMID: 24745676 PMCID: PMC5798580 DOI: 10.1016/j.iac.2014.01.005
Source DB: PubMed Journal: Immunol Allergy Clin North Am ISSN: 0889-8561 Impact factor: 3.479