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Dress syndrome following carbamazepine exposure: A very early onset

Published online by Cambridge University Press:  13 August 2021

M. Kraiem*
Affiliation:
Psychiatry C, Hedi Chaker University Hospital, sfax, Tunisia
N. Charfi
Affiliation:
Psychiatry C Department, Hedi chaker University hospital, sfax, Tunisia
E. Mhiri
Affiliation:
Hedi Chaker, psychiatry department, sfax, Tunisia
I. Gassara
Affiliation:
Psychiatry C, Hedi Chaker University Hospital, sfax, Tunisia
S. Omri
Affiliation:
Psychiatry C Department, Hedi chaker University hospital, sfax, Tunisia
N. Smaoui
Affiliation:
Psychiatry C Department, Hedi chaker University hospital, sfax, Tunisia
R. Feki
Affiliation:
Psychiatry C Department, Hedi chaker University hospital, sfax, Tunisia
L. Zouari
Affiliation:
Psychiatry C Department, Hedi chaker University hospital, sfax, Tunisia
J. Ben Thabet
Affiliation:
Psychiatry C Department, Hedi chaker University hospital, sfax, Tunisia
M. Maalej Bouali
Affiliation:
Psychiatry C Department, Hedi chaker University hospital, sfax, Tunisia
M. Maalej
Affiliation:
Psychiatry C Department, Hedi chaker University hospital, sfax, Tunisia
*
*Corresponding author.

Abstract

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Introduction

Drug reaction with eosinophilia and systemic symptoms (DRESS) is a severe cutaneous drug reaction characterised by both systemic and cutaneous clinical manifestation with a mean latency period of 3.9 weeks.

Objectives

To underline the importance of an early diagnosis of DRESS SYNDROME.

Methods

We reported a case of carbamazepine induced DRESS syndrome with atypical chronology of manifestations.

Results

A 43-year-old man with no previous known medical history was admitted in psychiatry. He experienced a relapse of schizoaffective symptoms. In the last three years, the patient was treated by Valproic acid as a mood stabilizer. Because of the unavailability of this molecule, carbamazepine was prescribed in combination with antipsychotics. Three days later, the patient developed a high fever, hypotension, a pruritus, a facial oedema, a skin rash associated to lymphadenopathy. Laboratory findings showed a lymphopenia, eosinophilia and elevated liver chemistries. In order to define the case, RegiSCAR scoring system was used, and our case is categorized as probable with a score of five. Carbamazepine was discontinued upon clinical manifestationsand the patient was treated with systemic antihistaminic treatment associated to methylprednisolone with a good outcome. After 3 weeks, clinical and biological improvement were noted.

Conclusions

Despite the absence of a delayed onset, typically between 3 weeks and 3months, we can diagnose dress syndrome 3 days after carbamazepine intake. This case highlights that psychiatrists should be aware of the risk of early onset dress syndrome associated with carbamazepine and they should monitor for warning symptoms from treatment initiation.

Disclosure

No significant relationships.

Type
Abstract
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
© The Author(s), 2021. Published by Cambridge University Press on behalf of the European Psychiatric Association
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