1.
Indian J Pathol Microbiol
;
2014 Oct-Dec 57 (4): 661-662
Artículo
en Inglés
| IMSEAR
| ID: sea-156169
2.
Indian J Pathol Microbiol
;
2011 Jul-Sept 54(3): 609-611
Artículo
en Inglés
| IMSEAR
| ID: sea-142058
RESUMEN
Apparent hemoglobinopathy acquired after blood transfusion is an uncommon cause of diagnostic dilemma resulting in repeated testing and delay in the diagnosis. Out of the 1530 hemoglobin (Hb)- high-performance liquid chromatography (HPLC) performed at our hospital (May 2009 to April 2010), 3 pediatric cases of thalassemia major were detected having posttransfusion hemoglobinopathy with HbS ranging from 9.9% to 18.5%. In all three cases, there was no variant hemoglobin in earlier documented Hb-HPLC. It is important to be aware of and consider apparent transfusion-induced hemoglobinopathy in patients with unusual percentage of variant hemoglobin to avoid unnecessary treatment and counseling.
Asunto(s)
Transfusión Sanguínea/efectos adversos , Preescolar , Cromatografía Líquida de Alta Presión , Hemoglobinopatías/diagnóstico , Hemoglobinopatías/patología , Hemoglobinas/química , Humanos , Lactante , Masculino , Talasemia beta/complicaciones , Talasemia beta/terapia
3.
Artículo
en Inglés
| IMSEAR
| ID: sea-64265