Your browser doesn't support javascript.
loading
Quetiapine Induced Autoimmune Hemolytic Anemia in a Child Patient: A Case Report
Clinical Psychopharmacology and Neuroscience ; : 501-504, 2018.
Artigo em Inglês | WPRIM | ID: wpr-718209
ABSTRACT
Autoimmune hemolytic anemia is a disease characterized with destruction of erythrocytes as a result of antibody produce against patient's own erythrocytes and anemia. Autoimmune hemolytic anemia can be roughly stratified into two groups according to serological features and secondary causes including drugs induced hemolytic anemia. Drugs induced autoimmune hemolytic anemia is very rare in pediatric patients. Even though hematological side effects such as leucopenia, agranulocytosis, eosinophilia, thrombocytopenic purpura and aplastic anemia might occur due to psychotropic drug use; to the best of our knowledge there is no autoimmune hemolytic anemia case due to quetiapine, an atypical antipsychotics, in literature. We hereby describe the first child case of autoimmune hemolytic anemia during quetiapine treatment.We also are pointing out that one should keep in mind serious hematological side effects with atypical antipsychotic drug use with this case report.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Púrpura Trombocitopênica / Antipsicóticos / Agranulocitose / Eosinofilia / Eritrócitos / Fumarato de Quetiapina / Anemia / Anemia Aplástica / Anemia Hemolítica / Anemia Hemolítica Autoimune Limite: Criança / Humanos Idioma: Inglês Revista: Clinical Psychopharmacology and Neuroscience Ano de publicação: 2018 Tipo de documento: Artigo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Púrpura Trombocitopênica / Antipsicóticos / Agranulocitose / Eosinofilia / Eritrócitos / Fumarato de Quetiapina / Anemia / Anemia Aplástica / Anemia Hemolítica / Anemia Hemolítica Autoimune Limite: Criança / Humanos Idioma: Inglês Revista: Clinical Psychopharmacology and Neuroscience Ano de publicação: 2018 Tipo de documento: Artigo