Autoimmune Hemolytic Anemia after Aplastic Crisis due to Parvovirus B19 Infection in a Patient with Hereditary Spherocytosis
Laboratory Medicine Online
; : 166-169, 2012.
Article
de Ko
| WPRIM
| ID: wpr-145045
Bibliothèque responsable:
WPRO
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.
Mots clés
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Arthrite
/
Maladies auto-immunes
/
Sphérocytes
/
Sphérocytose héréditaire
/
Membrane cellulaire
/
Érythème infectieux
/
Parvovirus
/
Protéines du cytosquelette
/
Anémie hémolytique
/
Anémie hémolytique auto-immune
Limites du sujet:
Child
/
Humans
langue:
Ko
Texte intégral:
Laboratory Medicine Online
Année:
2012
Type:
Article