Transfusion independence after repeated haploidentical hematopoietic cell transplants in a patient with congenital dyserythropoietic anemia type II and hemosiderosis.
Marci MacaraegMaria ProytchevaEmmanuel KatsanisPublished in: Pediatric transplantation (2019)
Matched related or unrelated donor allogeneic HCT has occasionally been applied in patients with severe CDA type II and proven to be curative. We report on the first patient with CDA to undergo haploidentical bone marrow transplantation with PT-CY. A 12-year-old boy with severe hemosiderosis, and a, consequently, disturbed BM microenvironment, developed recurrent graft failures and required salvage with two additional haploidentical HCTs. He achieved complete donor chimerism and transfusion independence after the third HCT. Our case underscores the risks associated with performing haploidentical HCT in older pediatric patients with CDA and severe chronic iron overload.
Keyphrases
- bone marrow
- stem cell transplantation
- mesenchymal stem cells
- early onset
- case report
- peripheral blood
- high dose
- cardiac surgery
- drug induced
- cell cycle arrest
- cord blood
- stem cells
- chronic kidney disease
- single cell
- sickle cell disease
- young adults
- cell death
- allogeneic hematopoietic stem cell transplantation
- acute lymphoblastic leukemia
- climate change