Frenzel K, Amann G, Lubec B
University of Vienna, Department of Neonatology, Austria.
Arch Dis Child. 1998 Jun;78(6):557-9. doi: 10.1136/adc.78.6.557.
A dysmorphic infant is described who presented with laryngeal collapse leading to intubation and respiratory problems that were assigned clinically to the Sussman syndrome. The baby had repeated episodes of respiratory distress necessitating assisted ventilation. At 6 months old, uvulopharyngopalatotomy was done to enlarge the supraglottic airway without any benefit. Surgical reduction of the tongue and cricoid splitting did not ameliorate the respiratory distress; repeated extubation attempts failed with the baby developing stridor, respiratory distress, and episodes of cardiac arrest. At 10 months old he developed seizures and computed tomography showed diffuse cerebral atrophy consisted with hypoxic-ischaemic damage. He died at 17 months old. Western blots using antibodies against collagen alpha 1 (II) showed an absence of collagen type II in laryngeal tissue, which may explain the laryngeal collapse and impaired respiratory functions.
本文描述了一名畸形婴儿,其因喉部塌陷导致插管及呼吸问题,临床上被诊断为萨斯曼综合征。该婴儿反复出现呼吸窘迫,需要辅助通气。6个月大时,进行了悬雍垂腭咽成形术以扩大声门上气道,但未取得任何效果。手术缩小舌头和环状软骨裂开并未改善呼吸窘迫;反复拔管尝试均失败,婴儿出现喘鸣、呼吸窘迫及心脏骤停发作。10个月大时,他出现癫痫发作,计算机断层扫描显示弥漫性脑萎缩,符合缺氧缺血性损伤。他于17个月大时死亡。使用抗胶原蛋白α1(II)抗体的蛋白质免疫印迹显示喉部组织中不存在II型胶原蛋白,这可能解释了喉部塌陷及呼吸功能受损的原因。