抄録
Selective neutropenia lasting over five months occurred in a 17-year- old adolescent male who received all allogeneic bone marrow transplantation (BMT) from an HLA-identical sibling for severe aplastic anemia. Bone marrow specimens showed maturation arrest of myeloid precursor cells despite sustained engraftment. Cytogenetic analyses revealed complete donor-type chimerism in hematopoietic cells and mixed lymphoid chimerism. The patient received a second BMT from the same donor following more intensive conditioning, including total body irradiation. neutrophil recovery was rapid and complete donor-type hematopoietic and lymphoid chimerism was observed within three weeks of the second transplant. The present case suggests that prolonged selective neutropenia following BMT is due to residual host- derived immunity which is resistant to the standard immunosuppressive conditioning used prior to BMT for asplastic anemia.
| 本文言語 | 英語 |
|---|---|
| ページ(範囲) | 513-516 |
| ページ数 | 4 |
| ジャーナル | International Journal of Hematology |
| 巻 | 66 |
| 号 | 4 |
| DOI | |
| 出版ステータス | 出版済み - 12-1997 |
| 外部発表 | はい |
All Science Journal Classification (ASJC) codes
- 血液学
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