Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD.
Hematology Am Soc Hematol Educ Program. 2017 Dec 8;2017(1):242-250. doi: 10.1182/asheducation-2017.1.242.
The clinical manifestations of inherited susceptibility to leukemia encompass a wide phenotypic range, including patients with certain congenital anomalies or early-onset myelodysplastic syndrome (MDS) and some with no obvious medical problems until they develop leukemia. Leukemia susceptibility syndromes occur as a result of autosomal dominant, autosomal recessive, or X-linked recessive inheritance, or de novo occurrence, of germline pathogenic variants in DNA repair, ribosome biogenesis, telomere biology, hematopoietic transcription factors, tumor suppressors, and other critical cellular processes. Children and adults with cytopenias, MDS, dysmorphic features, notable infectious histories, immunodeficiency, certain dermatologic findings, lymphedema, unusual sensitivity to radiation or chemotherapy, or acute leukemia with a family history of early-onset cancer, pulmonary fibrosis, or alveolar proteinosis should be thoroughly evaluated for a leukemia susceptibility syndrome. Genetic testing and other diagnostic modalities have improved our ability to identify these patients and to counsel them and their family members for subsequent disease risk, cancer surveillance, and therapeutic interventions. Herein, the leukemia susceptibility syndromes are divided into 3 groups: (1) those associated with an underlying inherited bone marrow failure syndrome, (2) disorders in which MDS precedes leukemia development, and (3) those with a risk primarily of leukemia. Although children are the focus of this review, it is important for clinicians to recognize that inherited susceptibility to cancer can present at any age, even in older adults; genetic counseling is essential and prompt referral to experts in each syndrome is strongly recommended.
遗传性白血病易感性的临床表现包括广泛的表型范围,包括具有某些先天异常或早发性骨髓增生异常综合征 (MDS) 的患者和一些在发生白血病之前没有明显医疗问题的患者。白血病易感性综合征是由于 DNA 修复、核糖体生物发生、端粒生物学、造血转录因子、肿瘤抑制因子和其他关键细胞过程中的常染色体显性、常染色体隐性或 X 连锁隐性遗传或新生种系致病性变异引起的。具有血细胞减少症、MDS、畸形特征、显著感染史、免疫缺陷、某些皮肤发现、淋巴水肿、对辐射或化疗异常敏感或具有家族史的早发性癌症、肺纤维化或肺泡蛋白沉积症的儿童和成人应彻底评估白血病易感性综合征。遗传检测和其他诊断方式提高了我们识别这些患者的能力,并为他们及其家庭成员提供了随后的疾病风险、癌症监测和治疗干预的咨询。在此,将白血病易感性综合征分为 3 组:(1) 与潜在遗传性骨髓衰竭综合征相关的综合征,(2) MDS 先于白血病发展的疾病,和 (3) 主要与白血病相关的疾病。虽然儿童是本综述的重点,但临床医生必须认识到遗传性癌症易感性可发生在任何年龄,甚至在老年人群中;遗传咨询至关重要,并强烈建议将患者转介给每个综合征的专家。