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再生障碍性贫血和骨髓增生异常综合征国际基金会(AA&MDSIF):2018 年骨髓衰竭性疾病科学研讨会。

Aplastic Anemia & MDS International Foundation (AA&MDSIF): Bone Marrow Failure Disease Scientific Symposium 2018.

机构信息

Pediatric Hematology/Oncology/Blood and Bone Marrow Transplant Division, Medical College of Wisconsin, 8701 Watertown Plank Road, MFRC 3020, Milwaukee, WI, 53226, United States.

Aplastic Anemia & Myelodysplastic Syndrome International Foundation, 4330 East West Highway, Suite 230, Bethesda, MD, United States.

出版信息

Leuk Res. 2019 May;80:19-25. doi: 10.1016/j.leukres.2019.03.003. Epub 2019 Mar 20.

Abstract

The bone marrow failure (BMF) syndromes are a group of rare disorders characterized by ineffective hematopoiesis resulting from deficiencies in the hematopoietic stem cell compartment. Although these diseases are typically acquired, some forms (e.g., Fanconi anemia, dyskeratosis congenita, Diamond Blackfan anemia, and Shwachman Diamond syndrome) are inherited. Patients with BMF syndromes can develop peripheral blood cytopenias and pancytopenia, and their disease can ultimately progress to acute myelogenous leukemia (AML). Research around the world is shedding light on the biology of the BMF syndromes, their clinical effects, and novel treatments. The Aplastic Anemia and MDS International Foundation (AAMDSIF) is an independent nonprofit organization whose mission is to help patients and family members cope with BMF syndromes. This report summarizes presentations on the latest scientific discoveries in BMF syndromes from the Sixth International Bone Marrow Failure Disease Scientific Symposium sponsored by AAMDSIF on March 22-23, 2018, in Rockville, Maryland.

摘要

骨髓衰竭(BMF)综合征是一组罕见疾病,其特征为造血干细胞区系缺陷导致无效造血。尽管这些疾病通常是获得性的,但有些形式(例如范可尼贫血、先天性角化不良、先天性纯红细胞再生障碍性贫血和 Shwachman-Diamond 综合征)是遗传性的。BMF 综合征患者可出现外周血细胞减少和全血细胞减少,其疾病最终可进展为急性髓系白血病(AML)。世界各地的研究正在揭示 BMF 综合征的生物学、临床效应和新的治疗方法。再生障碍性贫血和 MDS 国际基金会(AAMDSIF)是一个独立的非营利组织,其使命是帮助患者及其家属应对 BMF 综合征。本报告总结了 2018 年 3 月 22 日至 23 日在马里兰州罗克维尔举行的由 AAMDSIF 赞助的第六届国际骨髓衰竭疾病科学研讨会关于 BMF 综合征最新科学发现的演讲。

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