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Clozapine-associated eosinophilia with multiple systemic involvement - case report and review of literature

Published online by Cambridge University Press:  13 August 2021

I. Orlović*
Affiliation:
Department Of Psychiatry, Sestre Milosrdnice University Hospital Center, Zagreb, Croatia
T. Sugnet
Affiliation:
Department Of Psychiatry, Sestre Milosrdnice University Hospital Center, Zagreb, Croatia
M. Peco
Affiliation:
Department Of Psychiatry, Sestre Milosrdnice University Hospital Center, Zagreb, Croatia
V. Golubić Zatezalo
Affiliation:
Department Of Psychiatry, Sestre Milosrdnice University Hospital Center, Zagreb, Croatia
H. Karlica
Affiliation:
Department Of Psychiatry, University Hospital Center Split, Split, Croatia
D. Karlović
Affiliation:
Department Of Psychiatry, Sestre Milosrdnice University Hospital Center, Zagreb, Croatia
*
*Corresponding author.

Abstract

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Introduction

Due to its mood-stabilizing properties, clozapine is known for reducing symptom severity in manic episodes of treatment-resistant bipolar disorder as well as in treatment-resistant schizophrenia. However, its use may be hindered by potential adverse effects, including hematologic ones, such as non-dose-dependent eosinophilia. The mechanism of the underlying process probably involves a type-I hypersensitivity reaction, which can manifest as either transient asymptomatic eosinophilia or as eosinophilia with multiorgan dysfunction.

Objectives

We present the case of a patient diagnosed with manic episode of schizoaffective disorder who developed eosinophilia, with severe systemic manifestations, in response to clozapine therapy. A review of literature will be conducted in order to provide further insight into the phenomenon.

Methods

Case report and literature review.

Results

The incidence of eosinophilia reported in literature ranges between 0.2% and 62%, with its appearance about three weeks after clozapine initiation. Although clozapine is an antipsychotic that normally requires frequent monitoring due to the potential side effect of agranulocytosis, we would like to place emphasis on the possible risk of eosinophilia, in connection with potential fatal complications. As described in this report, eosinophilia could long remain unrecognized due to subsequent multiorgan involvement, including lymphadenopathy, leukocytosis, lymphopenia, anemia, liver enzyme elevations, as well as pleural effusion, all of which were described in our patient.

Conclusions

Clozapine-associated eosinophilia may be used as an early marker of possible clozapine-induced systemic complications and it may warrant prompt discontinuation of the causing drug, as suggested by the literature.

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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