2023, Number 2
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Rev Fac Med UNAM 2023; 66 (2)
DRESS, a Non-IgE Mediated Allergic Reaction
Pavón-Romero GF, Gutiérrez-Quiroz KV, Ramírez-Jiménez F, Rosas-Fernández R, Parra-Vargas MI, Terán LM
Language: Spanish
References: 40
Page: 7-19
PDF size: 470.07 Kb.
ABSTRACT
DRESS (drug reaction syndrome with eosinophilia and
systemic symptoms) is a rare drug-induced multisystemic
hypersensitivity response that can induce a severe cutaneous
adverse reaction that is difficult to diagnose and treat.
It frequently manifests as an extensive skin rash, systemic
symptoms, lymphadenopathy, visceral organ involvement,
and hematological alterations, mainly leukocytosis, eosinophilia,
and sometimes atypical lymphocytosis that manifest
2 to 8 weeks after continuous administration of the responsible
drug. The most prevalent drugs related with this
syndrome are phenytoin, carbamazepine, allopurinol, and
abacavir. Some specific human leukocyte antigen (HLA)
alleles have been identified that are associated with hypersensitivity
to these drugs. The pathophysiology of DRESS
syndrome is not yet fully understood; the main hypothesis
is a T-cell mediated hypersensitivity response when interacting
with the major histocompatibility complex receptor
in individuals with genetic susceptibility factors. The criteria
of the
European Registry of Severe Cutaneous Adverse Reactions
to Drugs (RegiSCAR) are the most commonly used for
the diagnosis of DRESS syndrome. Drug-induced hypersensitivity
syndrome (DiHS), Stevens-Johnson syndrome (SJS),
toxic epidermal necrolysis (TEN), and acute generalized
exanthematous pustulosis (AGEP) should be considered
for any rash that appears following the administration of
any drug. Therapy of DRESS includes the elimination of the
causative agent as soon as possible, as well as systemic
corticosteroids which are the cornerstones of treatment.
Steroid-sparing agents such as cyclosporine, intravenous
immunoglobulins (IVIGs), and other immunosuppressive
agents have been used successfully to contribute to treatment.
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