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P10.  CARBAMAZEPINE-INDUCED DRUG REACTION WITH
               EOSINOPHILIA AND SYSTEMIC SYMPTOMS (DRESS)

               SYNDROME: THE VALUE OF PATCH TESTING IN DIAGNOSIS
               - A CASE SERIES


               R. SLIM1, F. CHAHED1, N. FATHALLAH1, N. AMORRI 1, S. MOKNI 2, N. FETOUI GHARIANI
               2, M. DENGUEZLI2, C. BEN SALEM1, B. OUNI1

                1.  DEPARTMENT        OF       PHARMACOVIGILANCE,         METABOLICBIOPHYSICS         AND
                   APPLIEDPHARMACOLOGYLABORATORY (LR12ES02), FACULTY OF MEDICINE OF SOUSSE,
                   UNIVERSITY OF SOUSSE, TUNISIA
                2.  DEPARTMENT OF DERMATOLOGY, FARHAT HACHEDUNIVERSITY HOSPITAL, SOUSSE, TUNISIA



               INTRODUCTION  :  DRESS syndrome is  a  potentially life-threatening
               hypersensitivity reaction commonly associated with the use of antiepileptic drugs
               especially carbamazepine, an aromatic anticonvulsant.

               OBJECTIVE  :  We  present  a case series of patients who  developed DRESS
               syndrome after exposure to carbamazepine and emphasize the usefulness of the
               patch test (PT) in confirming the diagnosis.

               METHOD : We included all cases of DRESS related to carbamazepine notified to
               the pharmacovigilance  department of  the University Hospital of  Sousse-Tunisia
               over a period of 6 years (2017-2022).

               RESULTS : 13 patients (8F /5M) were included in this study. The median age was
               50 years [15-74 years]. The median time interval between the onset of symptoms
               and the onset of DRESS was 54 days [11-180 days]. Underlying atopy was presented
               in one patient. All patients presented with diffuse maculopapular exanthema and
               pruritus. Pustular eruptions were observed in three patients. Mucosal involvement
               was noted in 2 patients. Fever and lymphadenopathy were noted in 7 and 4 patients
               respectively. Eosinophilia was identified in 10 patients. Hepatic involvement with
               cytolysis was present in 10 patients and associated with cholestasis in 7 patients.
               Two patients had  acute renal  failure. Rhabdomyolysis  was  noted in 5 patients.
               Dyspnea was found in 3 patients. A high level of serum lipase was identified in one
               patient. To manage the condition, carbamazepine was immediately withdrawn in
               all patients. Treatment  with prednisone and antihistaminic  therapy  was
               administered in  9 patients. Blood  cell  counts, renal  functions, blood pressures,
               heart rates, body temperatures, and oxygen saturation throughout the course of
               treatment  were  monitored  in all patients. Skin biopsies were  performed in 7
               patients and were consistent with DRESS syndrome. The clinical and biological
               course was favorable in all patients. The imputability  of carbamazepine  was
               probable in all cases. PTs were performed on 10 patients and were positive at the
               72 reading, in 9 patients. To investigate the cross-reactivity between the aromatic
               anticonvulsants (Phenytoin, phenobarbital, Lamotrigine), PTs were carried out and
               revealed negative in 100% of cases. After a period of 3 years, a patient experienced


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