A Case of Hereditary Spherocytosis with Hemolytic Anemia due to Mycoplasma pneumonia / 소아감염
Korean Journal of Pediatric Infectious Diseases
; : 215-219, 2009.
Article
en Ko
| WPRIM
| ID: wpr-55867
Biblioteca responsable:
WPRO
ABSTRACT
Mycoplasma pneumoniae is a common cause of community-acquired pneumonia in children, with a peak incidence at 5-14 years. Extrapulmonary manifestations occur in 20-25% of patients with M. pneumoniae infection. Most auto-antibodies that cause immune hemolytic anemia in humans are cold agglutinins. The formation of cold agglutinins is frequently observed during M. pneumoniae infections, and cold agglutinin disease usually occurs during M. pneumoniae infections. Nevertheless, severe hemolysis is exceptional. If a patient has any underlying disease related to hemolysis, it is possible to accelerate hemolysis. Hereditary spherocytosis is a common cause of hereditary hemolytic anemia resulting from red blood cell membrane defects. Hemolysis of red cells may result from corpuscular abnormalities or extracorpuscular abnormalities, such as immune or non-immune mechanisms. We report a case of hereditary spherocytosis associated with severe hemolytic anemia due to Mycoplasma pneumonia.
Palabras clave
Texto completo:
1
Índice:
WPRIM
Asunto principal:
Neumonía
/
Neumonía por Mycoplasma
/
Esferocitosis Hereditaria
/
Crioglobulinas
/
Incidencia
/
Frío
/
Aglutininas
/
Eritrocitos
/
Hemólisis
/
Anemia Hemolítica
Tipo de estudio:
Incidence_studies
/
Prognostic_studies
Límite:
Child
/
Humans
Idioma:
Ko
Revista:
Korean Journal of Pediatric Infectious Diseases
Año:
2009
Tipo del documento:
Article