Autoimmune Hemolytic Anemia after Aplastic Crisis due to Parvovirus B19 Infection in a Patient with Hereditary Spherocytosis
Laboratory Medicine Online
;
: 166-169, 2012.
Artigo
em Coreano
| WPRIM
| ID: wpr-145045
ABSTRACT
Hereditary spherocytosis (HS) is a genetic disorder characterized by the production and destruction of spherocytes due to a deficiency of red cell membrane cytoskeletal proteins, resulting in the clinical presentation of chronic hemolytic anemia. This disease can be accompanied by an aplastic crisis due to parvovirus B19 infection. Parvovirus B19 infection causes diseases such as erythema infectiosum and arthritis, and can also trigger various autoimmune diseases, including autoimmune hemolytic anemia (AIHA). Here, we report a rare case of AIHA developing 3 months after an aplastic crisis due to parvovirus B19 infection in an 11-year-old boy with HS and provide the relevant literature review.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Artrite
/
Doenças Autoimunes
/
Esferócitos
/
Esferocitose Hereditária
/
Membrana Celular
/
Eritema Infeccioso
/
Parvovirus
/
Proteínas do Citoesqueleto
/
Anemia Hemolítica
/
Anemia Hemolítica Autoimune
Limite:
Criança
/
Humanos
Idioma:
Coreano
Revista:
Laboratory Medicine Online
Ano de publicação:
2012
Tipo de documento:
Artigo
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