Source. Diagnosis established upon demonstration of the major criterion combined with at least one minor criterion (and absence of any other disease better accounting for the problems).
Major Criterion:
- Constellation of clinical complaints attributable to pathologically increased mast cell activity (mast cell mediator release syndrome)
Minor Criteria:
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Multifocal or disseminated infiltrates of mast cells in marrow and/or extracutaneous organ(s) (e.g., gastrointestinal or genitourinary tract; >19 mast cells/high power field)
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Abnormal spindle-shaped morphology in >25% of mast cells in marrow or other extracutaneous organ(s)
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Abnormal mast cell expression of CD2 and/or CD25 (i.e., co-expression of CD117/CD25 or CD117/CD2)
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mast cell genetic changes (e.g., activating KIT codon 419, 509 or 560 mutations) shown to increase mast cell activity
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Evidence (typically from body fluids such as whole blood, serum, plasma, or urine) of above-normal levels of mast cell mediators including: tryptase, histamine or its metabolites (e.g., N-methylhistamine), heparin, chromogranin A (note potential confounders of cardiac or renal failure, neuroendocrine tumors, recent proton pump inhibitor use, or chronic atrophic gastritis), other relatively mast cell-specific mediators (e.g., ecosanoids including prostaglandin (PG) D2, its metabolite 11-B-PGF2a, or leukotriene E4)
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Symptomatic response to inhibitors of mast cell activation or mast cell mediator production or action.