| Literature DB >> 11090093 |
S Matthes-Martin1, C Peters, A Königsrainer, G Fritsch, T Lion, A Heitger, K Kapelari, M Kronberger, F Offner, F Wrba, R Margreiter, H Gadner.
Abstract
The case of a 4-month-old girl with familial hemophagocytic lymphohistiocytosis is described. The patient underwent stem cell transplantation from her haploidentical mother 2 months after receiving a living-related liver transplant from the same donor for acute hepatic failure. Conditioning regimen consisted of 16 mg/kg busulfan, 200 mg/kg cyclophosphamide, 10 mg/kg thiothepa, and antithymocyte globulin. Myeloid engraftment occurred on day +10, but CD3(+) cells of recipient origin remained. To convert the T-cell chimerism, the patient received donor lymphocyte infusion on day +43, and subsequently the allelic pattern changed to complete donor genotype on day +57. Four months after stem cell transplantation the patient is disease free, with complete donor chimerism in bone marrow and stable hepatic graft function without any immunosuppressive therapy. (Blood. 2000;96:3997-3999)Entities:
Mesh:
Year: 2000 PMID: 11090093
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113