prev next front |1 |2 |3 |4 |5 |6 |7 |8 |9 |10 |11 |12 |13 |14 |15 |16 |17 |18 |19 |20 |21 |22 |23 |24 |25 |26 |27 |28 |29 |30 |31 |32 |33 |34 |35 |36 |37 |38 |39 |40 |41 |42 |43 |44 |45 |review
The diagnosis of anaphylaxis is made in the clinical setting on the basis of clinical presentation. Cutaneous and respiratory findings occur in at least 60% of subjects described in 7 retrospective series encompassing 1217 subjects. Urticaria and angioedema are the most common manifestations and the absence of either should prompt a physician to consider another diagnosis, except perhaps where food-induced anaphylaxis is suspected.

The diagnosis can be confirmed in doubtful cases by the demonstration of the presence of elevated plasma concentrations of the mast cell enzyme, tryptase, which is specific for mast cell degranulation. Tryptase remains elevated for up to six hours following anaphylaxis, is stable while refrigerated, and may be assayed in serum previously obtained for other purposes. Although serum tryptase may not be elevated in food-related anaphylaxis.