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Severe hemolytic transfusion reaction due to anti-D in a D+ patient with sickle cell disease
A 5-year-old male with sickle cell disease presented with pain, dark urine, and fatigue 10 days after a red blood cell (RBC) transfusion. Laboratory evaluation demonstrated severe anemia, blood type O+, and anti-D in the serum. Anti-D in a D+ patient led to RH genotyping which revealed homozygosity...
Gorde:
| Argitaratua izan da: | J Pediatr Hematol Oncol |
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| Egile Nagusiak: | , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2015
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4333075/ https://ncbi.nlm.nih.gov/pubmed/25171447 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MPH.0000000000000241 |
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