一名青少年因无症状气胸继发霍纳综合征。

Horner's syndrome secondary to asymptomatic pneumothorax in an adolescent.

作者信息

Mutalib Mohamed, Vandervelde Clive, Varghese Ajay, Sallomi David F, de Silva Padmani, Hickman Casey J M, Howlett David C

机构信息

Department of Paediatrics, Eastbourne District General Hospital, Kings Drive, Eastbourne, East Sussex, UK.

出版信息

Eur J Pediatr. 2007 May;166(5):507-8. doi: 10.1007/s00431-006-0271-4. Epub 2006 Sep 19.

DOI:10.1007/s00431-006-0271-4

PMID:17047992

Abstract

Horner's syndrome is uncommon in the paediatric population, but is seen more in infancy, and most cases are either congenital or related to birth trauma, head and neck tumours or thoracic surgery. We report an unusual cause of Horner's syndrome in a healthy adolescent boy secondary to a large, spontaneous, but asymptomatic, primary pneumothorax.

摘要

霍纳综合征在儿科人群中并不常见，但在婴儿期更为多见，且大多数病例为先天性或与产伤、头颈部肿瘤或胸外科手术有关。我们报告了一名健康青少年男性因巨大、自发性但无症状的原发性气胸继发霍纳综合征这一不寻常病因。