Hannah-Shmouni Fady, Stratakis Constantine A
Section on Endocrinology & Genetics (SEGEN), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD, 20892, USA.
Curr Opin Endocr Metab Res. 2018 Aug;1:19-24. doi: 10.1016/j.coemr.2018.04.002. Epub 2018 Apr 24.
Pituitary adenomas in children and adolescents are rare tumors that often result from a tumor predisposition syndrome. Several inherited causes for pituitary adenomas have been identified in the last few years, including multiple endocrine neoplasia type 1 and 4, Carney's complex, Tuberous sclerosis, DICER1 syndrome, neurofibromatosis type 1, McCune Albright syndrome, familial isolated pituitary adenoma, and pituitary adenoma association due to defects in succinate dehydrogenase genes. Recently, our group discovered X-linked acrogigantism (X-LAG), a new pediatric disorder that is caused by an Xq26.3 genomic duplication (involving the gene). Genes that predispose to pediatric Cushing disease, including and , were also recently identified. Genetic screening and counseling of affected or at risk individuals is a key component of their comprehensive care. In this review, we provide an up-to-date discussion on the latest pediatric genetic discoveries associated with pituitary adenomas with a focus on familial syndromes.
儿童和青少年垂体腺瘤是罕见肿瘤,通常由肿瘤易感性综合征引起。过去几年已确定了垂体腺瘤的几种遗传病因,包括1型和4型多发性内分泌腺瘤病、卡尼综合征、结节性硬化症、DICER1综合征、1型神经纤维瘤病、麦库恩-奥尔布赖特综合征、家族性孤立性垂体腺瘤以及由于琥珀酸脱氢酶基因缺陷导致的垂体腺瘤关联。最近,我们的研究小组发现了X连锁肢端肥大症(X-LAG),这是一种由Xq26.3基因组重复(涉及 基因)引起的新型儿科疾病。最近还发现了易患儿童库欣病的基因,包括 和 。对受影响或有风险的个体进行基因筛查和咨询是其综合治疗的关键组成部分。在本综述中,我们提供了关于与垂体腺瘤相关的最新儿科遗传学发现的最新讨论,重点是家族性综合征。