Goldenhar综合征中罕见的双叶后舌表现。
Rare presentation of bilobed posterior tongue in Goldenhar syndrome.
作者信息
Rajendran Thilaga, Ramalinggam Ganesh, Kamaru Ambu Valuyeetham
机构信息
Otorhinolaryngology, Hospital Tuanku Ja'afar, Seremban, Negeri Sembilan, Malaysia.
出版信息
BMJ Case Rep. 2017 Aug 1;2017:bcr-2017-219726. doi: 10.1136/bcr-2017-219726.
Abstract
A bilobed posterior tongue is a rare malformation with few reported cases in the literature. This anomaly has not been demonstrated in patients with Goldenhar syndrome. We report a case of a 5-month-old child with the classic signs of Goldenhar syndrome and laryngomalacia with an incidental finding of a bilobed posterior tongue. Careful assessment and monitoring are crucial, especially in syndromic babies.
摘要
双侧叶后舌是一种罕见的畸形，文献中报道的病例很少。在Goldenhar综合征患者中尚未证实存在这种异常。我们报告一例5个月大的儿童，具有Goldenhar综合征和喉软化症的典型体征，偶然发现双侧叶后舌。仔细评估和监测至关重要，尤其是对于患有综合征的婴儿。
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