Harlequin syndrome and Horner syndrome after neck schwannoma excision in a pediatric patient

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Harlequin syndrome and Horner syndrome after neck schwannoma excision in a pediatric patient

RATIONALE Harlequin syndrome is an extremely rare benign condition characterized by unilateral facial flushing and sweating. PATIENT CONCERN An 11-year-old boy presented with complaint of a right neck mass of 1-month duration. DIAGNOSIS The preoperative diagnosis was neurogenic tumor of vagus nerve or sympathetic nerve. INTERVENTIONS We performed right neck mass removal under general anes...

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Late Postoperative Harlequin Syndrome Coexisting With Horner Syndrome After Thoracic Epidural Anesthesia

The predominant features of Harlequin syndrome are unilateral facial flushing and sweating. Harlequin syndrome has been reported in different clinical conditions including brain stem infarction, superior mediastinal neurinoma, and internal jugular vein catheterization.1,2 Idiopathic and iatrogenic cases have been reported. The clinical features of Horner syndrome are ptosis, miosis, enophthalmo...

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Horner syndrome after radical neck surgery for anaplastic thyroid carcinoma.

To cite: Sandoval MAS, Cabungcal AC. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2015209324 DESCRIPTION A 63-year-old woman presented with a right anterior neck mass that enlarged rapidly over 2 months. She had dysphagia but did not have hoarseness, dyspnoea or thyrotoxic symptoms. Preoperative CT scan revealed a 7.6×8.8×7.3 cm mass, well-defined, heterogeneou...

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A pediatric case of idiopathic Harlequin syndrome

Harlequin syndrome, which is a rare disorder caused by dysfunction of the autonomic system, manifests as asymmetric facial flushing and sweating in response to heat, exercise, or emotional factors. The syndrome may be primary (idiopathic) with a benign course, or can occur secondary to structural abnormalities or iatrogenic factors. The precise mechanism underlying idiopathic harlequin syndrome...

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Pediatric Horner syndrome and neuroblastoma threat.

T he article byJeffery et al. 1 on pages 159-67 of this issue of the Journal of AAPOS raises interesting points regarding pediatric Horner syndrome. On the basis of a retrospective review of 73 patients less than 18 years old seen over 10 years at two large referral centers, the authors provide a diagnostic paradigm emphasizing that seemingly idiopathic cases should be thoroughly investigated f...

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ژورنال

عنوان ژورنال: Medicine

سال: 2017

ISSN: 0025-7974

DOI: 10.1097/md.0000000000008548