Tufano Maria, Della Corte Claudia, Cirillo Francesco, Spagnuolo Maria Immacolata, Candusso Manila, Melis Daniela, Torre Giuliano, Iorio Raffaele
Pediatric Liver Unit, Department of Pediatrics, University of Naples Federico II, Via S. Pansini 5, 80131 Naples, Italy.
Eur J Pediatr. 2009 Feb;168(2):225-7. doi: 10.1007/s00431-008-0732-z. Epub 2008 May 14.
We report a 7-year-old girl with 22q13 deletion syndrome, 46,XX,Ish del(22)(q13.3)(ARSA-; D22S1726), who developed a fulminant autoimmune hepatitis requiring orthotopic liver transplantation. Recently, it has been suggested that the Shank3 gene product, whose deficiency is responsible for the features observed in this syndrome, could play a role in immunological response. Despite an increased incidence of respiratory infections, autoimmune diseases have thus far not been reported in patients with this syndrome. This is the first case of fulminant autoimmune hepatitis associated with the 22q13 deletion syndrome. The possible relationships between immune system dysfunctions peculiar of this syndrome and autoimmune hepatitis are discussed.
我们报告了一名患有22q13缺失综合征的7岁女孩,核型为46,XX,Ish del(22)(q13.3)(ARSA-; D22S1726),她患上了暴发性自身免疫性肝炎,需要进行原位肝移植。最近,有人提出,该综合征所观察到的特征是由Shank3基因产物缺乏所致,它可能在免疫反应中发挥作用。尽管该综合征患者呼吸道感染的发生率有所增加,但迄今为止尚未有自身免疫性疾病的报道。这是首例与22q13缺失综合征相关的暴发性自身免疫性肝炎病例。本文讨论了该综合征特有的免疫系统功能障碍与自身免疫性肝炎之间可能的关系。