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2例呈现7号染色体单体克隆性造血的婴儿的脐血移植:SAMD9 / SAMD9L种系突变

Cord Blood Transplantation in 2 Infants Presenting Monosomy 7 Clonal Hematopoiesis: SAMD9 / SAMD9L Germline Mutation.

作者信息

Hirai Maiko, Yagasaki Hiroshi, Kanezawa Koji, Ueno Masaru, Shimozawa Katsuyoshi, Imai Kohsuke, Morio Tomohiro, Kato Motohiro, Gocho Yoshihiro, Narumi Satoshi, Ebihara Yasuhiro, Morioka Ichiro

机构信息

Department of Pediatrics and Child Health, Nihon University Itabashi Hospital.

Department of Pediatrics, Tokyo Medical and Dental University.

出版信息

J Pediatr Hematol Oncol. 2023 Mar 1;45(2):e290-e293. doi: 10.1097/MPH.0000000000002578. Epub 2022 Oct 21.

Abstract

Recently, germline mutations in SAMD9 and SAMD9L were increasingly found in children with monosomy 7. We report the outcomes in 2 infants with the SAMD9/SAMD9L variant, who presented with anemia and thrombocytopenia (patient 1), and neutropenia and nonsymptomatic white-matter-encephalopathy (patient 2). Both patients received cord blood transplantation and experienced critical post-cord blood transplantation adverse events; patients 1 and 2 developed fulminant engraftment syndrome and life-threatening graft-versus-host disease, respectively. Of note, selective loss of chromosome 7 in bone marrow-derived CD34 + cells was inferred.

摘要

最近,在7号染色体单体症患儿中越来越多地发现SAMD9和SAMD9L的种系突变。我们报告了2例携带SAMD9/SAMD9L变异的婴儿的情况,其中1例表现为贫血和血小板减少(患者1),另1例表现为中性粒细胞减少和无症状白质脑病(患者2)。两名患者均接受了脐血移植,并经历了严重的脐血移植后不良事件;患者1和患者2分别发生了暴发性植入综合征和危及生命的移植物抗宿主病。值得注意的是,推测骨髓来源的CD34 +细胞中7号染色体选择性缺失。

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