青少年骨髓增生异常综合征。

S S Winter, P Mathew, R L Vaughan, K Foucar
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引用次数: 0

摘要

骨髓增生异常综合征(MDS)是一组由骨髓功能异常引起的获得性血液病。红细胞、血小板和白细胞的无效产生可导致症状性贫血、瘀伤、感染,并有可能演变为急性骨髓性白血病。虽然MDS在青少年患者中并不常见,但令人惊讶的是,受影响的个体也受到易感体质综合征的影响。青少年MDS患者的治疗部分取决于症状,也取决于与五种表现形态类别相关的历史结果。改善的支持性护理使越来越多的MDS患儿存活到生命的第二个十年。在受影响的青少年MDS的管理提出了一些有趣的和有价值的挑战,卫生保健专业人员。
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Myelodysplastic syndromes in the adolescent.

Myelodysplastic syndromes (MDS) are a group of acquired blood diseases that are the result of abnormal bone marrow function. The ineffective production of red cells, platelets, and white blood cells can lead to symptomatic anemia, bruising, infections, and the likelihood of evolution into acute myelogenous leukemia. While MDS is uncommon in the adolescent patient, a surprising number of affected individuals are also affected with a predisposing constitutional syndrome. The treatment of MDS in the adolescent patient is in part determined by symptoms and also by the historical outcomes associated with each of five morphologic categories of presentation. Improved supportive care has allowed for increasingly more children with MDS to survive into the second decade of life. The management of MDS in affected adolescents presents a number of interesting and worthwhile challenges to health care professionals.

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