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Allergy Asthma Immunol Res. 2010 April; 2(2): 123–126.
Published online 2010 March 24. doi:  10.4168/aair.2010.2.2.123
PMCID: PMC2846735

Comparison of the Causes and Clinical Features of Drug Rash With Eosinophilia and Systemic Symptoms and Stevens-Johnson Syndrome

Abstract

Purpose

Drug rash with eosinophilia and systemic symptoms (DRESS) and the Stevens-Johnson syndrome (SJS) are both severe drug reactions. Their pathogenesis and clinical features differ. This study compared the causes and clinical features of SJS and DRESS.

Methods

We enrolled 31 patients who were diagnosed with DRESS (number=11) and SJS (number=20). We retrospectively compared the clinical and laboratory data of patients with the two disorders.

Results

In both syndromes, the most common prodromal symptoms were itching, fever, and malaise. The liver was commonly involved in DRESS. The mucosal membrane of the oral cavity and eyes was often affected in SJS. The most common causative agents in both diseases were antibiotics (DRESS 4/11 (37%), SJS 8/20 (40%)), followed by anticonvulsants (DRESS 3/11 (27%), SJS 7/20 (35%)). In addition, dapsone, allopurinol, clopidogrel, sulfasalazine and non-steroidal anti-inflammatory drugs (NSAIDs) were sporadic causes.

Conclusions

The most common causes of DRESS and SJS were antibiotics, followed by anticonvulsants, NSAIDs and sulfonamides. The increase in the use of antibiotics in Korea might explain this finding.

Keywords: Drug hypersensitivity, DRESS syndrome, Stevens-Johnson syndrome

INTRODUCTION

The drug rash with eosinophilia and systemic symptoms (DRESS) syndrome, previously referred to as the 'drug hypersensitivity syndrome', is an adverse drug reaction characterized by skin rash, fever, lymph-node enlargement and internal organ involvement.1 The definition of DRESS is flawed in that it does not characterize the nature of the cutaneous rash. Aromatic anticonvulsants (phenytoin, phenobarbital, carbamazepine) and sulfonamides are the most common causes of DRESS.2

The differential diagnosis includes Stevens-Johnson syndrome (SJS), which is a rare, life-threatening, cutaneous adverse reaction. SJS is characterized by targetoid cutaneous lesions affecting less than 10% of the body surface area. There is mucous membrane involvement in approximately 90% of the affected patients.3 The risk factors for SJS include infection, vaccination, drugs, systemic diseases, physical agents and food. SJS has been associated with more than 100 drugs based on case reports and studies.4

DRESS and SJS are similar in that the clinical manifestations typically occur within 2 to 6 weeks after initiating drug therapy.1 However, the two syndromes have different characteristics, treatments and prognoses. Here, we compare the causes and clinical features of DRESS and SJS.

MATERIALS AND METHODS

Patients and methods

Records of the patients who were hospitalized with a diagnosis of DRESS or SJS from April 2004 to March 2008 were reviewed. The diagnosis of DRESS or SJS was based on the presence of a relationship between drug intake and the time to cutaneous adverse reactions. Moreover, the diagnosis of DRESS was based on the existence of associated systemic involvement and the presence of eosinophilia (>500/mm3 or >10%).5,6 The diagnosis of SJS was based on severe skin lesions (mucous membrane erosions, target lesions and epidermal necrosis with skin detachment) affecting less than 10% of the total body surface, regardless of the laboratory findings. The diagnosis was confirmed by a histopathological analysis of focal tissue (vacuolization of basal layer keratinocytes associated with lymphocytes).5,7,8

DRESS and SJS are differentiated by the nature of the skin lesions and extent of body surface area involvement over other criteria. Considering an appropriate differential diagnosis in patients with mucocutaneous erosions can help prevent misdiagnoses associated with cutaneous adverse drug reactions.

Statistics

Statistical analysis was performed using SPSS version 17.0 for Windows (SPSS, Chicago, IL, USA). Data are expressed as the mean and standard error of the mean. Fisher's exact test and the Mann-Whitney U-test were used for categorical and continuous variables, respectively. Personal characteristics and disease-related factors were compared between the disorders. The association of laboratory tests with the two disorders was adjusted for the 95% confidence interval as the effect measure. A P value of less than 0.05 was considered statistically significant.

RESULTS

Patient characteristics

The study included 31 adults hospitalized with a diagnosis of DRESS or SJS. Eleven patients (4 men, 7 women; median age 51.5 years) had DRESS and 20 patients (12 men, 8 women; median age of 58.5 years) had SJS. There were no significant differences in the baseline values between the two disorders (Table 1).

Table 1
Clinical characteristics of the study subjects

Clinical findings

For DRESS syndrome, patients had prodromal symptoms of itching, fever and facial edema. Patients with SJS commonly had prodromal symptoms of fever and malaise. The first skin lesions appeared on the extremities and face in DRESS and on the trunk in SJS (Table 2). The trunk lesions in SJS were tender. The mucosal membranes of the oral cavity and eyes were commonly affected in SJS. The genitalia (2/19, 10.5%) and anus (2/19, 10.5%) were also affected (Table 3A).

Table 2
Clinical data
Table 3
Mucosal involvement in SJS and systemic manifestations in DRESS syndrome

The results of laboratory tests

The liver was involved in DRESS, and all patients with DRESS had elevated liver enzymes. The kidneys (2/11, 18.2%) were also involved (Table 3B).

In differentiating between DRESS and SJS, the skin lesions are considered first. Two patients with SJS had eosinophilia (>500/mm3 or >10%) and 17 had elevated liver enzymes (ALT or AST >40 U/L).

Causative drugs

The most common causative drugs were antibiotics, which were identified as the cause in 4 of 11 patients (36%) with DRESS and 8 of 20 patients (40%) with SJS. From most to least common, the four antibiotics that were involved most frequently were vancomycin, ceftriaxone, rifampin, ciprofloxacin and Bactrim. Anticonvulsants were the second most common drugs involved; 3 (27%) cases of DRESS and 7 (35%) of SJS were associated with anticonvulsants. From most to least common, the four anticonvulsants that were involved most frequently were lithium, carbamazepine, lamotrigine and oxcarbazepine. The remaining drugs involved in both disorders were herbal medications (10%), allopurinol, clopidogrel and sulfonamide. In addition, dapsone (18%) and NSAIDs were associated with the development of DRESS (Table 4).

Table 4
Causative drugs

Treatment and outcome

Patients with DRESS with internal organ involvement were treated with corticosteroids (7 patients, 64%) and dramatic improvement was observed. Most patients recovered in the absence of specific treatment after eliminating the causative drug. Most patients with SJS were successfully treated conservatively or with corticosteroids. Six patients (30%) were treated with antibiotics and one patient relapsed and died.

DISCUSSION

This study compared the causes and clinical features of DRESS and SJS. DRESS is a major cause of hospitalization for dermatological complications in patients treated with anticonvulsants.10 The clinical manifestations typically occur within 2 to 6 weeks after initiating drug therapy and most cases resolve without sequelae when the drug is discontinued. The outcome is fatal in 5-10% of cases. The most common clinical presentation of DRESS includes fever, eruption and lymphadenopathy. The most common hematological abnormalities are eosinophilia, leukocytosis and lymphocytosis. Liver involvement in patients with DRESS may range from a transitory increase in liver enzymes to liver necrosis with fulminant hepatic failure. Only transitory hepatitis was observed in our study, and the patients recovered without sequelae. Other potentially fatal complications are hypersensitivity myocarditis, pericarditis, pneumonitis and nephritis.6,11,12

Although there are a variety of etiologies, such as infections and underlying malignancies, drugs remain the predominant cause of SJS. The most commonly implicated drugs are anticonvulsants, sulfa derivatives, NSAIDs, penicillins, cephalosporins and allopurinols.1,9 The characteristic skin lesions seen in SJS are diffuse erythematous macules with purpuric, necrotic centers, and overlying blistering. These cutaneous lesions often demonstrate a positive Nikolsky sign, which is further detachment of the epidermis with slight lateral pressure. Painful erosions of the mucous membranes are common and may affect the lips, oral cavity, conjunctiva, nasal cavity, urethra, vagina, gastrointestinal tract and respiratory tract during the course of the illness. The mucosal membranes most often affected in our study were the oral cavity and eyes. SJS is fatal in 5-15% of cases.3,8 Both the incidence of the condition and the associated mortality appear to be increased in immunocompromised patients.

DRESS and SJS are part of a spectrum of adverse cutaneous drug reactions. However, the pathophysiology of DRESS and SJS has not been elucidated fully. Various theories have been proposed, including both immunological and non-immunological mechanisms.3,13 The current pathophysiological explanation for DRESS is immunological. Drugs with reactive metabolites can modify cellular proteins and target an autoimmune response against the skin or liver cells.11 It now appears that the immunological mechanisms associated with SJS are initiated by the Fas antigen, a cell surface molecule that can mediate apoptosis.3

Laboratory testing can help to identify internal organ involvement, which may not be evident clinically. A skin biopsy may help to confirm the diagnosis, but is usually not specific. The suspected drug should be discontinued immediately when these two syndromes are being considered.1,8,12 Delaying this measure may be associated with a poor outcome. For patients with extensive mucocutaneous involvement, prompt referral to a burn unit is recommended.

Corticosteroids remain the agents most widely used for treating DRESS, although the doses used vary widely across case reports.8 Favorable results have been reported with their use. In the absence of a well-established therapy, primary and secondary prevention have key roles in the management of these two syndromes.1,8 Milder cases of SJS can be managed in an inpatient setting using the same fundamental therapeutic protocol used for the treatment of burns. The use of medications to treat SJS remains controversial. Treatment with corticosteroids, while effective in most other acute inflammatory disorders, is controversial.

The most important diagnostic clues are the mucosal lesions and eosinophilia, characteristic of both syndromes. Age and gender were not helpful in differentiating SJS from DRESS. Elevated liver enzymes suggest the DRESS syndrome, well known to affect internal organs. As in a previous study, the liver was commonly involved in our DRESS patients. However, some earlier studies reported that up to 75% of the patients with SJS had elevated liver enzymes, similar to patients with DRESS.14 Hepatitis was observed in 85% of the patients with SJS in our study. Anticonvulsants were once the most common cause although, more recently, antibiotics have been reported to be the most common cause of both disorders.6,8,9 The increase in the use of antibiotics in Korea might explain this finding. After prompt withdrawal of the offending drug, conservative treatment or combination corticosteroid treatment has been used to treat patients with both syndromes, and most patients have improved clinical symptoms and laboratory findings with this approach. In the absence of specific treatment, the elimination of the causative drug and proper symptomatic treatment are the best management approaches for both SJS and DRESS.

Footnotes

There are no financial or other issues that might lead to conflict of interest.

References

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Articles from Allergy, Asthma & Immunology Research are provided here courtesy of Korean Academy of Asthma, Allergy and Clinical Immunology and Korean Academy of Pediatric Allergy and Respiratory Disease