1.
Indian J Pathol Microbiol
; 2014 Oct-Dec 57 (4): 661-662
Article
in English
| IMSEAR
| ID: sea-156169
2.
Indian J Pathol Microbiol
; 2011 Jul-Sept 54(3): 609-611
Article
in English
| IMSEAR
| ID: sea-142058
ABSTRACT
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.
Subject(s)
Blood Transfusion/adverse effects , Child, Preschool , Chromatography, High Pressure Liquid , Hemoglobinopathies/diagnosis , Hemoglobinopathies/pathology , Hemoglobins/chemistry , Humans , Infant , Male , beta-Thalassemia/complications , beta-Thalassemia/therapy
3.
Article
in English
| IMSEAR
| ID: sea-64265