Paediatric Horner Syndrome: How much further to investigate?
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...
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Veröffentlicht in: | Indian journal of ophthalmology 2020-11, Vol.68 (11), p.2607-2610 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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. |
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ISSN: | 0301-4738 1998-3689 |
DOI: | 10.4103/ijo.IJO_1603_20 |