Autoimmune Hemolytic Anemia after Aplastic Crisis due to Parvovirus B19 Infection in a Patient with Hereditary Spherocytosis
Laboratory Medicine Online
;
: 166-169, 2012.
Artículo
en 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:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Artritis
/
Enfermedades Autoinmunes
/
Esferocitos
/
Esferocitosis Hereditaria
/
Membrana Celular
/
Eritema Infeccioso
/
Parvovirus
/
Proteínas del Citoesqueleto
/
Anemia Hemolítica
/
Anemia Hemolítica Autoinmune
Límite:
Niño
/
Humanos
Idioma:
Coreano
Revista:
Laboratory Medicine Online
Año:
2012
Tipo del documento:
Artículo
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