医学
含铁血黄素沉着症
贫血
骨髓衰竭
造血干细胞移植
骨髓
外科
造血
移植
干细胞
内科学
遗传学
生物
作者
Marci Macaraeg,Maria Proytcheva,Emmanuel Katsanis
摘要
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.
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