Drug reaction with eosinophilia and systemic symptoms
Drug reaction with eosinophilia and systemic symptoms (DRESS syndrome) is a syndrome, caused by exposure to certain medications, that may cause a rash, fever, inflammation of internal organs, lymphadenopathy, and characteristic hematologic abnormalities such as eosinophilia, thrombocytopenia, and atypical lymphocytosis. The syndrome carries about a 10% mortality.[1] Treatment consists of stopping the offending medication and providing supportive care. Systemic steroids are commonly used as well; however, there are no controlled clinical trials to assess the efficacy of this treatment.[2]
The term was coined in a 1996 report in an attempt to simplify terminology for a syndrome recognized as early as 1959.[3][4]
Nomenclature
DRESS is one of several terms that have been used to describe a severe idiosyncratic reaction to a drug that is characterized by a long latency of onset after exposure to the offending medication, a rash, involvement of internal organs, hematologic abnormalities, and systemic illness. Other synonymous names and acronyms include HSS (Hypersensitivity Syndrome), AHS (Anticonvulsant Hypersensitivity Syndrome), DIHS (Drug-Induced Hypersensitivity Syndrome), DIDMOHS (Drug-Induced Delayed Multiorgan Hypersensitivity Syndrome), and Drug-Induced Pseudolymphoma.[1]
Signs and symptoms
The symptoms of DRESS syndrome usually begin several weeks after exposure to the offending drug. There is no gold standard for diagnosis, and at least two diagnostic criteria have been proposed. The RegiSCAR criteria [5] and the Japanese consensus group criteria[6] are detailed in the table below.
RegiSCAR inclusion criteria for DRESS syndrome. Three of the four starred criteria required for diagnosis | Japanese consensus group diagnostic criteria for DIHS. Seven criteria needed for diagnosis of DIHS or the first five criteria required for diagnosis of atypical DIHS |
---|---|
Hospitalization | Maculopapular rash developing > 3 weeks after starting the suspected drug |
Reaction suspected to be drug-related | Prolonged clinical symptoms 2 weeks after discontinuation of the suspected drug |
Acute Rash* | Fever > 38 °C |
Fever > 38 °C* | Liver abnormalities (ALT > 100 U/L) or other organ involvement |
Lymphadenopathy in at least two sites* | Leukocyte abnormalities |
Involvement of at least one internal organ* | Leukocytosis ( > 11 x 109/L) |
Blood count abnormalities (lymphopenia or lymphocytosis*, eosinophilia*, thrombocytopenia*) | Atypical lymphocytosis (>5%) |
Lymphadenopathy | |
Human herpesvirus 6 reactivation |
Symptoms may be severe and involve many different organs. In a retrospective Taiwanese cohort study of 60 patients,[7] the following incidences were observed.
Incidence of organ involvement in DRESS syndrome [1] | |
---|---|
Organ | Percent of patients with involvement |
Liver | 80% |
Kidney | 40% |
Pulmonary | 33% |
Cardiac/muscular | 15% |
Pancreas | 5% |
Incidence of hematologic abnormalities in DRESS syndrome [1] | |
---|---|
Abnormality | Percent of patients with abnormality |
Atypical lymphocyte | 63% |
Eosinophilia | 52% |
Lymphocytopenia | 45% |
Thrombocytopenia | 25% |
Lymphocytosis | 25% |
Causes
Drugs that commonly induce DRESS syndrome include phenobarbital, carbamazepine, phenytoin,[8] lamotrigine, minocycline,[9] sulfonamides, allopurinol,[10] modafinil, dapsone, ziprasidone,[11] and most recently olanzapine.[12] It has been associated with HHV-6 reactivation.[13]
See also
References
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Further reading
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- ↑ Volume 14, Issue 8, Pages 498-500 (December 2003)