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Year : 2015  |  Volume : 47  |  Issue : 6  |  Page : 687--689

Drug reaction with eosinophilia and systemic symptoms without skin rash

Sarita Sasidharanpillai1, Manikoth P Binitha1, Neeraj Manikath2, Anisha K Janardhanan1,  
1 Department of Dermatology and Venereology, Government Medical College, Kozhikode, Kerala, India
2 Department of General Medicine, Government Medical College, Kozhikode, Kerala, India

Correspondence Address:
Dr. Sarita Sasidharanpillai
Department of Dermatology and Venereology, Government Medical College, Kozhikode, Kerala
India

Abstract

Drug reaction with eosinophilia and systemic symptoms (DRESS) or drug hypersensitivity syndrome is considered as a severe cutaneous adverse drug reaction which is most commonly precipitated by aromatic anticonvulsants, lamotrigine, dapsone, allopurinol, minocycline, and salazopyrin. Its clinical manifestations are often variable. On rare occasions, it can present with only systemic involvement without any cutaneous features. A complete drug history is of paramount importance in making an early diagnosis. We report the case of a male patient who presented with fever, lymphadenopathy, hepatosplenomegaly, and hepatitis, 2 weeks after starting salazopyrin. The presence of atypical lymphocytes in the peripheral smear was indicative of a viral infection or a hematological dyscrasia. Bone marrow examination revealed a normocellular marrow with an increase in eosinophil precursors. Investigations for the common causes for fever and hepatitis were negative. The presence of eosinophilia, the temporal relationship of the symptoms with the initiation of treatment with salazopyrin, and the marked improvement on withdrawal of the drug along with the administration of systemic corticosteroids, were features consistent with the diagnosis of DRESS. With the incidence of this condition showing a rising trend, it is important for the clinician to be aware of its variable manifestations, as a delay in diagnosis and treatment can be fatal.



How to cite this article:
Sasidharanpillai S, Binitha MP, Manikath N, Janardhanan AK. Drug reaction with eosinophilia and systemic symptoms without skin rash.Indian J Pharmacol 2015;47:687-689


How to cite this URL:
Sasidharanpillai S, Binitha MP, Manikath N, Janardhanan AK. Drug reaction with eosinophilia and systemic symptoms without skin rash. Indian J Pharmacol [serial online] 2015 [cited 2021 Oct 21 ];47:687-689
Available from: https://www.ijp-online.com/text.asp?2015/47/6/687/169580


Full Text

 Introduction



Drug reaction with eosinophilia and systemic symptoms (DRESS) is a milder form of drug-induced hypersensitivity syndrome.[1] It can present in various or unusual clinical patterns [1],[2] which may confuse the clinician since diagnosis is based mainly on the exclusion of other possible diseases. We report a case of DRESS induced by salazopyrin where the absence of a rash led to diagnostic difficulty.

 Case Report



A 31-year-old man presented with high-grade fever, cough, jaundice, and vomiting of 5 days duration. His drug history included prednisolone 10 mg daily and salazopyrin 500 mg twice daily by mouth for the past 2 weeks, and hydroxychloroquin 200 mg twice daily by mouth for the past 1-year for pain in the right knee joint, which had been diagnosed as reactive arthritis.

On clinical examination, the patient was febrile, with a temperature of 42°C. There were multiple enlarged, firm, tender, mobile, anterior cervical and axillary lymph nodes ranging in size from 2 cm × 2 cm to 1 cm × 1 cm, as well as hepatosplenomegaly. There were no cutaneous lesions.

A complete blood count revealed a leukocytosis of 21,000 cells/mm,[3] comprising of 82% neutrophils, and an elevated absolute eosinophil count of 1822 cells/µl (normal: 450/µl). His liver function tests were deranged, with levels of total bilirubin 5.8 mg/dL (normal: 0.2–1.2 mg/dL), conjugated bilirubin 4 mg/dL (normal: 0.1–0.4 mg/dL) aspartate transaminase 221 IU/ml (normal: 10–40 IU/ml), and alanine transaminase 247 IU/ml (normal: 7–56 IU/ml).

Urine microscopy, renal function tests, blood sugar and serum pancreatic enzyme levels, chest X-ray and electrocardiogram were all within normal limits. Bacterial cultures of urine and blood were sterile. Serology for antinuclear antibody and antibodies to human immune deficiency virus, hepatitis A, B, and C viruses, Epstein–Barr virus, dengue virus, chikungunya virus, typhoid, leptospira, and rickettsiae were all negative. An ultrasonogram of the abdomen confirmed the hepatosplenomegaly.

A peripheral blood smear revealed atypical lymphocytes accounting for 30% of the peripheral lymphocytes and an eosinophilia of 10% (normal <7% of the circulating leukocytes) [Figure 1]a and [Figure 1]b. A cervical lymph node biopsy showed reactive hyperplasia. Bone marrow aspiration and trephine biopsy from the iliac crest showed respectively normocellular marrow and an increase in eosinophil precursors [Figure 2].{Figure 1}{Figure 2}

He was started on oral cefixime in a dose of 500 mg twice daily as an antibiotic cover. Since infective and autoimmune causes for the fever were not evident, the patient was suspected to have a drug allergy. As prednisolone and salazopyrine were the recently introduced drugs, they were stopped. Though cough and vomiting subsided, the fever persisted and repeated liver function tests on the 5th day of admission showed no improvement. A definite diagnosis of DRESS due to salazopyrin was made as per the registry of severe cutaneous adverse reactions (RegiSCAR) DRESS validation score.[2],[3] The causality was “probable” as per the Naranjo's adverse drug reaction probability scale.[4]

Treatment with oral prednisolone was initiated in a dose of 1 mg/kg body weight/day. Within 24 h, the fever had subsided, and the abnormal liver function tests steadily improved and normalized over the subsequent 4 weeks. The prednisolone was tapered slowly over 7 weeks so as to avoid the flare up of DRESS associated with rapid tapering of corticosteroids. A repeat abdominal ultrasonogram 2 months later revealed a normal study.

 Discussion



DRESS is considered a severe drug reaction with a case fatality rate of 10–20%.[5] The unique features of this condition include a long latent interval between the onset of drug intake and the appearance of symptoms (1-week to 3 months), persistence or even worsening of the symptoms in spite of the withdrawal of the culprit drug as noted in our case, and waxing and waning of the disease often necessitating prolonged treatment with systemic steroids.[5] It is described as a reaction pattern characterized by the triad of rash, systemic involvement and eosinophilia.[5] However, on rare occasions, it can present as a purely systemic disease without any cutaneous involvement.[6],[7] It can closely mimic viral exanthema or neoplastic or autoimmune diseases. In the absence of confirmatory diagnostic criteria, it remains a diagnostic challenge, especially in cases lacking a skin rash.

Currently, the RegiSCAR DRESS validation score is used to diagnose DRESS. One point each is assigned for: (1) Skin rash with two of the four features - facial edema, rash resolving with psoriasiform desquamation, purpuric lesions on areas other than the legs, and infiltrated skin lesions (2) rash involving >50% of the body surface (3) lymphadenopathy of size more than 1 cm, affecting two or more anatomic locations (4) the presence of atypical cells in the peripheral smear (5) eosinophilia in the range of 750–1499 cells/µl (6) involvement of one internal organ due to DRESS. If two or more internal organs are affected or eosinophilia is equal to or more than 1500 cells/µl, two points are added. If serology for antinuclear antibody, hepatitis A, B, and C infections are negative and the blood culture is sterile, one more point is added. One point each is reduced in the case of rash not suggestive of DRESS, skin biopsy conclusive of another diagnosis, the symptoms resolving within 15 days, and the absence of fever. As per this score, our patient had a RegiSCAR score of 6, sufficient to categorize him as a case of definite DRESS.[2],[3]

Patients with DRESS with mild or no skin involvement have been found to be immunocompromised - they were either receiving immunosuppressant drugs including prednisolone equal to or more than 10 mg/day or they were suffering from human immunodeficiency virus infection.[7] The concomitant administration of prednisolone 10 mg/day and hydroxychloroquin (which is an immune modulator drug) with salazopyrin might be the reason for the absence of rash in our case.

The possibility of hydroxychloroquin precipitating DRESS was unlikely in our case since the patient was on this drug for a year without any untoward effects, and his symptoms resolved in spite of continuing the drug. The rare possibility of prednisolone inducing the reaction was ruled out by the lack of symptoms on its reintroduction.

We report this case to highlight the significance of a detailed drug history whenever a patient presents with pyrexia of unknown origin and systemic complications, with or without a rash. Once diagnosed, DRESS can be managed by withdrawing the drug and administering steroids, but mere withdrawal of the drug will not arrest the disease process and a delay in starting steroid treatment may prove fatal.

Financial Support and Sponsorship

Nil.

Conflicts of Interest

There are no conflicts of interest.

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