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1.
Journal of the Korean Society of Neonatology ; : 99-102, 2003.
Artículo en Coreano | WPRIM | ID: wpr-27187

RESUMEN

The incidence of malaria in Korea is significantly on the rise since its reemergence in 1993 and no screening test that can prevent the infection has been available. Very low birth weight infants are especially susceptible to malaria infection due to transfusions from multiple donors. We report a case of transfusion transmitted Plasmodium vivax infection in a 120-day-old infant of a gestational age 24 weeks with birth weight of 700 gm who was successfully treated with hydroxychloroquine.


Asunto(s)
Humanos , Lactante , Peso al Nacer , Edad Gestacional , Hidroxicloroquina , Incidencia , Recién Nacido de muy Bajo Peso , Corea (Geográfico) , Malaria , Tamizaje Masivo , Plasmodium vivax , Donantes de Tejidos
2.
Korean Journal of Pediatric Hematology-Oncology ; : 262-268, 2003.
Artículo en Coreano | WPRIM | ID: wpr-194907

RESUMEN

PURPOSE: We investigated the expression of vasoactive intestinal peptide (VIP), VIP receptor 1 (VPAC1), VIP receptor 2 (VPAC2) genes in the human umbilical cord blood CD34 cells, and the ability of VIP to stimulate human primitive as well as monopotent hematopoietic progenitors. METHODS: We isolated RNA from umbilical cord blood CD34 cells, and then performed RT-PCR, and sequencing. The umbilical cord blood CD34 cells were cultured with the various concentrations of VIP for burst-forming unit of erythrocyte (BFU-E), colony-forming unit of granulocyte/monocyte (CFU-GM), colony-forming unit of graulocyte/erythrocyte/monocyte/megakaryocyte (CFU-GEMM), and colony-forming unit of megakaryocyte (CFU-Mk). RESULTS: The RNA coding for VPAC1 was detected in human umbilical cord blood CD34 cells. VIP significantly stimulated the growth of CFU-GEMM and CFU-Mk. CONCLUSION: The present results suggest that VIP is an important neuropeptide in the early proliferation of human primitive as well as megakaryocyte progenitors.


Asunto(s)
Humanos , Codificación Clínica , Eritrocitos , Sangre Fetal , Células Progenitoras de Megacariocitos , Megacariocitos , Células Progenitoras Mieloides , Neuropéptidos , Receptores de Péptido Intestinal Vasoactivo , ARN , Células Madre , Péptido Intestinal Vasoactivo
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