Horner Syndrome After Tonsillectomy: An Anatomic Perspective

被引:8
|
作者
Giannikas, Christina [1 ,2 ]
Pomeranz, Howard D. [1 ,2 ]
Smith, Lee P. [2 ,3 ]
Fefer, Zipora [2 ,4 ]
机构
[1] North Shore Long Isl Jewish Hlth Syst, Dept Ophthalmol, Great Neck, NY 11021 USA
[2] Hofstra North Shore LIJ Sch Med, Hempstead, NY USA
[3] North Shore Long Isl Jewish Hlth Syst, Cohen Childrens Med Ctr, Div Pediat Otolaryngol, New Hyde Pk, NY USA
[4] North Shore Long Isl Jewish Hlth Syst, Cohen Childrens Med Ctr, Div Pediat Neurol, New Hyde Pk, NY USA
关键词
Horner syndrome; anisocoria; ptosis; meiosis; anhidrosis; tonsillectomy; oculosympathetic paresis;
D O I
10.1016/j.pediatrneurol.2014.05.012
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND: Homer syndrome after tonsillectomy has been reported rarely in the literature. Furthermore, postoperative Homer syndrome lasting more than a 1 month is an even more rare occurrence. PATIENT: We present a persistent postoperative Homer syndrome in a 5-year-old child following tonsillectomy. RESULTS: Clinical diagnosis of Homer syndrome is confirmed pharmacologically, and damage to the oculosympathetic pathway at the level of the superior cervical ganglion is radiographically demonstrated. CONCLUSION: Conventional monopolar electrosurgical dissection led to irreversible damage of ganglionic neural tissue at the level of the palatine tonsilar fossa and permanent Homer syndrome.
引用
收藏
页码:417 / 420
页数:4
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