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婴儿淋巴管畸形伴后天性霍纳综合征

Lymphatic malformation with acquired Horner syndrome in an infant.

作者信息

Spors Birgit, Seemann Joerg, Homer Natalie, Fay Aaron

机构信息

Department of Pediatric Radiology, Klinik für Strahlenheilkunde, Charite Hospital, Berlin, Germany.

Clinic for Radiology and Neurosurgery, Klinikum Barnim GmbH, Werner Forssmann Krankenhaus, Eberswalde, Brandenburg, Germany.

出版信息

BMJ Case Rep. 2017 Oct 23;2017:bcr-2017-013315. doi: 10.1136/bcr-2017-013315.

Abstract

An infantpresented with right upper eyelid ptosis and was subsequently diagnosed with acquired Horner syndrome. Further evaluation revealed a right-sided cervicothoracic lymphatic malformation. At 13 weeks of age, the child underwent percutaneous intracystic sclerotherapy with a mixture of sodium tetradecyl sulphate and ethanol. Twenty-one weeks after initial treatment, ophthalmic examination showed complete resolution of the blepharoptosis and pupillary miosis. Percutaneous sclerotherapy not only effectively treated the space-occupying lymphatic malformation but also reversed the Horner syndrome that was presumably induced by neural tension (more likely) or compression.

摘要

一名婴儿出现右上睑下垂,随后被诊断为获得性霍纳综合征。进一步评估发现右侧颈胸段淋巴管畸形。患儿在13周龄时接受了十四烷基硫酸钠和乙醇混合液的经皮囊内硬化治疗。初始治疗21周后,眼科检查显示上睑下垂和瞳孔缩小完全消退。经皮硬化治疗不仅有效治疗了占位性淋巴管畸形,还逆转了可能由神经牵拉(更有可能)或压迫引起的霍纳综合征。

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