Kilic S Sebnem, Gurpinar Arif, Yakut Tahsin, Egeli Unal, Dogruyol Hasan
Immunology Unit, Department of Pediatrics, Uludag University School of Medicine, Bursa, Turkey.
J Pediatr Surg. 2003 Aug;38(8):E21-3. doi: 10.1016/s0022-3468(03)00295-1.
DiGeorge Syndrome (DGS) is a congenital disorder that affects the thymus, parathyroid glands, and heart and brain. Thymus involvement in DGS may vary between absence/hypoplasia of thymus to various forms of reduced T cell function. TBX1 deficiency causes a number of distinct vascular and heart defects, suggesting multiple roles in cardiovascular development, specifically, formation and growth of the pharyngeal arch arteries, growth and septation of the outflow tract of the heart, interventricular septation, and conal alignment. Here the authors describe a case of DGS presenting with severe combined immunodeficiency, esophageal atresia, and tracheoesophageal fistula (TEF). DGS is an important differential diagnosis in TEF.
迪乔治综合征(DGS)是一种先天性疾病,会影响胸腺、甲状旁腺以及心脏和大脑。DGS中胸腺受累情况可能有所不同,从胸腺缺如/发育不全到各种形式的T细胞功能降低。TBX1缺乏会导致多种明显的血管和心脏缺陷,表明其在心血管发育中具有多种作用,具体包括咽弓动脉的形成和生长、心脏流出道的生长和分隔、室间隔分隔以及圆锥排列。本文作者描述了一例伴有严重联合免疫缺陷、食管闭锁和气管食管瘘(TEF)的DGS病例。DGS是TEF的重要鉴别诊断疾病。