Anaphylaxis to quinolones in mastocytosis: Hypothesis on the mechanism
Genetic study for KIT mutation was not done. [...]SM without cutaneous involvement was diagnosed. [...]the frequency of clonal mast-cell disease in screened subjects with HVA ranges from 1% to 7.9%.4,5 The risk of anaphylaxis in mastocytosis increases with higher levels of tryptase. [...]more severe...
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Veröffentlicht in: | The journal of allergy and clinical immunology in practice (Cambridge, MA) MA), 2019-07, Vol.7 (6), p.2089-2090 |
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Sprache: | eng |
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Zusammenfassung: | Genetic study for KIT mutation was not done. [...]SM without cutaneous involvement was diagnosed. [...]the frequency of clonal mast-cell disease in screened subjects with HVA ranges from 1% to 7.9%.4,5 The risk of anaphylaxis in mastocytosis increases with higher levels of tryptase. [...]more severe Hymenoptera HSRs are also associated with higher baseline serum tryptase levels in patients without SM.4,5 Our patient had an abnormal serum tryptase level (17.7 μg/L). [...]the diagnosis is challenging, because drug-specific sIgE tests are unavailable and skin testing presents undetermined sensitivity and specificity.3 Quinolones are one of the substances that may activate mast cells through MRGPRX2, resulting in non–IgE-mediated release of mediators, as described above.7 In conclusion, the excess of mast cells and their MRGPRX2 receptors in patients with mastocytosis may induce anaphylaxis on activation by quinolones. |
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ISSN: | 2213-2198 2213-2201 |
DOI: | 10.1016/j.jaip.2019.01.059 |