Paediatric Horner Syndrome: How much further to investigate?

Abstract:

:We report an infant with an early-onset Horner syndrome and normal urinary catecholamine levels. Further investigations with Nuclear medicine imaging with123I-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.

journal_name

Indian J Ophthalmol

authors

Bhate M,Flaherty M,Rowe N,Howman-Giles R

doi

10.4103/ijo.IJO_1603_20

subject

Has Abstract

pub_date

2020-11-01 00:00:00

pages

2607-2610

issue

11

eissn

0301-4738

issn

1998-3689

pii

IndianJOphthalmol_2020_68_11_2607_299023

journal_volume

68

pub_type

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    journal_title:Indian journal of ophthalmology

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    更新日期:2015-08-01 00:00:00

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    更新日期:2020-12-01 00:00:00

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    pub_type: 杂志文章,评审

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    doi:

    authors: Ahmed M,Nasthi AR

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    更新日期:2014-02-01 00:00:00

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    更新日期:2014-07-01 00:00:00

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    更新日期:2012-01-01 00:00:00

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    authors: Karadag R,Sen A,Yildirim N,Basmak H,Golemez H,Cakir E,Akin A

    更新日期:2010-05-01 00:00:00

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    journal_title:Indian journal of ophthalmology

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    doi:

    authors:

    更新日期:1987-01-01 00:00:00

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    doi:

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    doi:

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    doi:10.4103/ijo.IJO_958_16

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