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[IgE mediated anaphylaxis in a patient with systemic mastocytosis].

Authors :
Escande H
Bennani I
Bulai Livideanu C
Uthurriague C
Paul C
Nougué J
Source :
Annales de dermatologie et de venereologie [Ann Dermatol Venereol] 2013 Oct; Vol. 140 (10), pp. 641-4. Date of Electronic Publication: 2013 Jun 24.
Publication Year :
2013

Abstract

Background: Anaphylaxis is a severe, generalized, life-threatening reaction of rapid onset. We report the case of a patient presenting several systemic anaphylactic reactions over many years, initially ascribed to a cereals allergy but which finally proved to be due to systemic mastocytosis hidden for a long time.<br />Patients and Methods: A 53-year-old man consulted for an eruption consisting of monomorphic pigmented maculopapular lesions on the trunk associated with itching and urticaria. He was a farmer and presented severe sensitivity to cereals, with anaphylaxis, which continued despite withdrawal of these allergens. Skin and bone marrow infiltration, abnormal mast cells, positivity for c-kit 816 mutation and the persistent elevation of serum tryptase enabled a diagnosis of indolent systemic mastocytosis to be made.<br />Discussion: In systemic mastocytosis anaphylaxis is an expected complication relating to the proliferation of mast cells and a massive increase in mediator release (non-immunological mechanism). All patients with severe and recurrent anaphylaxis should be analyzed for underlying mastocytosis by careful physical examination and assay of baseline tryptase.<br /> (Copyright © 2013 Elsevier Masson SAS. All rights reserved.)

Details

Language :
French
ISSN :
0151-9638
Volume :
140
Issue :
10
Database :
MEDLINE
Journal :
Annales de dermatologie et de venereologie
Publication Type :
Academic Journal
Accession number :
24090896
Full Text :
https://doi.org/10.1016/j.annder.2012.06.054