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先天性霍纳综合征:一例报告。

Congenital Horner's syndrome: report of one case.

作者信息

Sher J S, Jang C C

机构信息

Department of Pediatrics, Air Force General Hospital, Taipei, Taiwan, R.O.C.

出版信息

Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1992 Mar-Apr;33(2):144-7.

PMID:1514404
Abstract

Congenital Horner's syndrome is an infrequent illness caused by a lesion of the cervical sympathetic nerve fiber. It's clinical features are facial anhidrosis, ptosis, miosis, and hypochromia iridis of the affected side. The subject of this report, a full-term male newborn, had had a smooth birth process but was found on the second day of life to have narrowing of the palpebral fissure and absence of facial flushing on the right side when he cried. Ophthalmologic examination revealed a smaller right pupil. The above abnormalities proved to result from a post-ganglionic lesion, after pharmacologic test. Roentgenograms of the skull, chest and cervical spine were normal, and a computed tomography scan of the cervical spine showed no abnormalities. The diagnosis was of congenital Horner's syndrome. Since no congenital Horner's syndrome to the newborn period could be found in previous literature, this report is presented.

摘要

先天性霍纳综合征是一种由颈交感神经纤维损伤引起的罕见疾病。其临床特征为患侧面部无汗、上睑下垂、瞳孔缩小和虹膜色素减退。本报告的病例是一名足月男婴,出生过程顺利,但在出生后第二天被发现哭闹时右侧睑裂变窄且面部无潮红。眼科检查发现右侧瞳孔较小。经药物试验后,上述异常被证明是由节后神经损伤引起的。头颅、胸部和颈椎的X线片正常,颈椎计算机断层扫描未显示异常。诊断为先天性霍纳综合征。由于以往文献中未发现新生儿期先天性霍纳综合征的相关报道,故现呈上本报告。

相似文献

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Congenital Horner's syndrome: report of one case.先天性霍纳综合征:一例报告。
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