systemic mastocytosis associated with chronic idiopathic myelofibrosis

In approximately 20 to 30% of patients with systemic mastocytosis (SM), an associated clonal hematological nonmast cell lineage disorder (AHNMD) is diagnosed. SM may be considered to be closely related to the myeloproliferative disorders (MPDs).

See also

- KIT-D816V
- JAK2-V617F

References

- Systemic mastocytosis associated with chronic idiopathic myelofibrosis: a distinct subtype of systemic mastocytosis associated with a [corrected] clonal hematological non-mast cell lineage disorder carrying the activating point mutations KITD816V and JAK2V617F. Sotlar K, Bache A, Stellmacher F, Bültmann B, Valent P, Horny HP. J Mol Diagn. 2008 Jan;10(1):58-66. PMID: 18165278

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