Volume 23, Issue 8 e13587
CASE REPORT

Transfusion independence after repeated haploidentical hematopoietic cell transplants in a patient with congenital dyserythropoietic anemia type II and hemosiderosis

Marci Macaraeg

Marci Macaraeg

Department of Pediatrics, University of Arizona, Tucson, Arizona

Banner University Medical Center, Tucson, Arizona

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Maria Proytcheva

Maria Proytcheva

Banner University Medical Center, Tucson, Arizona

Department of Pathology, University of Arizona, Tucson, Arizona

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Emmanuel Katsanis

Corresponding Author

Emmanuel Katsanis

Department of Pediatrics, University of Arizona, Tucson, Arizona

Banner University Medical Center, Tucson, Arizona

Department of Pathology, University of Arizona, Tucson, Arizona

Department of Medicine, University of Arizona, Tucson, Arizona

Department of Immunobiology, University of Arizona, Tucson, Arizona

Correspondence

Emmanuel Katsanis, Department of Pediatrics, 1501 N. Campbell Ave., PO Box 245073, Tucson, AZ 85724-5073.

Email: [email protected]

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First published: 17 September 2019
Citations: 2

Abstract

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.

CONFLICT OF INTEREST

The authors declare no conflict of interest.

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