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施瓦赫曼-戴蒙德综合征与匹配的非亲属供者骨髓移植

Shwachman-Diamond syndrome and matched unrelated donor BMT.

作者信息

Smith O P, Chan M Y, Evans J, Veys P

机构信息

Department of Paediatric Haematology and Oncology, Great Ormond Street Hospital for Children NHS Trust, London, UK.

出版信息

Bone Marrow Transplant. 1995 Nov;16(5):717-8.

PMID:8547872
Abstract

A 5 year old with Shwachman-Diamond syndrome (SDS) developed acute monoblastic leukaemia following a period of myelodysplasia associated with a clonal cytogenetic abnormality involving chromosome 7. Matched unrelated BMT was carried out using standard CY/TBI conditioning and GVHD prophylaxis protocols. The patient experienced no toxicity, had temporary committed progenitor cell engraftment but eventually died from bone marrow failure 1 year post-transplant. This report, to our knowledge, documents the first reported case of matched unrelated donor BMT for SDS/AML and we speculate that standard conditioning regimens are probably safe in this group of patients.

摘要

一名5岁的施瓦赫曼-戴蒙德综合征(SDS)患儿,在经历了一段与涉及7号染色体的克隆性细胞遗传学异常相关的骨髓发育异常后,发展为急性单核细胞白血病。采用标准的环磷酰胺/全身照射预处理方案和移植物抗宿主病预防方案进行了匹配无关供体骨髓移植(BMT)。该患者未出现毒性反应,有短暂的定向祖细胞植入,但最终在移植后1年死于骨髓衰竭。据我们所知,本报告记录了首例关于SDS/AML的匹配无关供体BMT病例,我们推测标准预处理方案在这类患者中可能是安全的。

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