儿童霍纳综合征：还需要进一步检查多少？

Paediatric Horner Syndrome: How much further to investigate?

机构信息

Jasti V Ramanamma Children's Eye Care Centre L.V. Prasad Eye Institute, Hyderabad, Telangana, India.

Department of Ophthalmology Children's Hospital, Westmead, Australia.

出版信息

Indian J Ophthalmol. 2020 Nov;68(11):2607-2610. doi: 10.4103/ijo.IJO_1603_20.

DOI:10.4103/ijo.IJO_1603_20

PMID:33120710

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7774181/

Abstract

We report an infant with an early-onset Horner syndrome and normal urinary catecholamine levels. Further investigations with Nuclear medicine imaging withI-MIBG (meta-iodo benzyl-guanidine) confirmed a right thoracic inlet mass consistent with a neuroblastoma, a tumor of neural crest origin. The authors emphasize the need for investigating idiopathic acquired pediatric Horner syndrome and the value of an MIBG scan as a diagnostic test for suspected neuroblastoma.

摘要

我们报告了一例早发性霍纳综合征婴儿，其尿儿茶酚胺水平正常。进一步的核医学成像 I-MIBG（间碘苄胍）检查证实右侧胸廓入口处有一个神经母细胞瘤肿块，这是一种起源于神经嵴的肿瘤。作者强调了对特发性获得性儿科霍纳综合征进行调查的必要性，以及 MIBG 扫描作为疑似神经母细胞瘤诊断测试的价值。