Copyright
©The Author(s) 2021.
World J Clin Cases. Apr 26, 2021; 9(12): 2916-2922
Published online Apr 26, 2021. doi: 10.12998/wjcc.v9.i12.2916
Published online Apr 26, 2021. doi: 10.12998/wjcc.v9.i12.2916
Date | CBC | |
3 h and 56 min after birth | Blood cell count | |
RBC | 1.6 × 109/L | |
MCV | 132.5 fL | |
MCH | 40.6 pg | |
MCHC | 307 g/L | |
HGB | 65 g/L | |
Reticulocyte count | 0.477 × 106/L | |
Reticulocyte (%) | 29.78% | |
Bio-chemistry | ||
ALT | 55.0 U/L | |
AST | 273.0 U/L | |
Total bilirubin | 175.4 μmol/l | |
Unconjugated bilirubin | 159.8 μmol/L | |
Blood group | ||
Group O and Rh positive | ||
Blood group antibody screening | Negative | |
Others | ||
Coombs test | Negative | |
Free antibody test | Negative | |
Antibody release test | Negative | |
12 d old | ||
RBC | 3.7 × 109/L | |
HGB | 111 g/L | |
2 mo old | ||
HGB | HB 57 g/L |
Date | CBC | |
Before transplantation | Blood cell count | |
RBC | 5.7 × 109/L | |
HGB | 84 g/L | |
Bio-chemistry | ||
ALT | 23 U/L | |
AST | 46 U/L | |
Total bilirubin | 28.2 μmol/L | |
1 mo post transplantation | ||
WBC | 3.9 × 109/L | |
ANC | 1.23 × 109/L | |
HGB | 126 g/L | |
PLT | 109 × 109/L | |
2 mo post transplantation | ||
WBC | 2.7 × 109/L | |
ANC | 0.73 × 109/L | |
HGB | 118 g/L | |
PLT | 195 × 109/L | |
6 mo post transplantation | ||
WBC | 4.3 × 109/L | |
ANC | 1.52 × 109/L | |
HGB | 119 g/L | |
PLT | 150 × 109/L | |
1 year post transplantation | ||
WBC | 5.6 × 109/L | |
ANC | 1.89 × 109/L | |
HGB | 119 g/L | |
PLT | 169 × 109/L |
PKD | Thalassemia | |
Similarity | (1) Both are hemolytic anemia caused by gene abnormality; (2) Both can lead to severe hyperbilirubinemia in neonate period; and (3) Severe cases of both need transfusion regularly | |
Difference | ||
MCV | Normal | Smaller than the normal |
MCH | Normal | Smaller than the normal |
MACH | Normal | Smaller than the normal |
Hemoglobin electrophoresis | Normal | There are different abnormal bands according to different types |
Type of gene abnormality | Mutation of the PKLR gene which codes the enzyme of pyruvate kinase in red blood cells | Mutation of the gene which codes the globin chains |
- Citation: Ma ZY, Yang X. Allogeneic hematopoietic stem cell transplantation in a 3-year-old boy with congenital pyruvate kinase deficiency: A case report. World J Clin Cases 2021; 9(12): 2916-2922
- URL: https://www.wjgnet.com/2307-8960/full/v9/i12/2916.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v9.i12.2916