Literature DB >> 27148776

Horner Syndrome in Children: A Clinical Condition with Serious Underlying Disease.

Christophe Barrea1, Tiphaine Vigouroux1, Joe Karam1, Ariane Milet2, Sandrine Vaessen1, Jean-Paul Misson1.   

Abstract

Aim Horner syndrome corresponds to the clinical triad of miosis, ptosis, and facial anhidrosis. These symptoms are related to injury of the oculosympathetic chain. In children, Horner syndrome is classified as congenital or acquired. While the diagnosis is made through clinical examination, there is some debate regarding the use of imaging modalities and the extent of anatomical coverage required. Methods Here, we describe two cases of children with acute Horner syndrome. We then review the literature about the different etiology and discuss the interest of some investigations. Results Case 1: An 8-month-old girl without personal or familial history, has presented a right acquired Horner syndrome without additional signs. Frontal chest radiography and ultrasonography of the neck and the abdomen was first achieved and returned normal. The cerebral and cervical magnetic resonance imaging (MRI) with angiographic sequences performed in a second time was also normal. Finally, an enhanced thoracic computed tomography (CT)-scan demonstrated a mass at the right pulmonary apex. Case 2: A 9-year-old boy without personal or familial history has presented an acute headache with loss of consciousness during a basketball competition. Upon waking up, the child has right hemiplegia, aphasia, and left Horner syndrome. The cerebral CT scan realized in the first line was normal. The MRI with angiographic sequences demonstrated M1 left carotid dissection with homolateral white matter infarction. Conclusion Imaging studies seem critical in delineating the nature and extent of any underlying pathology along the oculosympathetic pathway in children presenting a Horner syndrome. In these patients, a history of trauma or surgery may reduce the need for extensive systemic evaluation. Without such anamnesis, a decision to proceed with further evaluation is made with consideration of the relative incidence of tumor, especially neuroblastoma, or other treatable lesions. In this condition, MRI is the more sensitive and recommended investigation. Georg Thieme Verlag KG Stuttgart · New York.

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Year:  2016        PMID: 27148776     DOI: 10.1055/s-0036-1584085

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  4 in total

1.  Ptosis, miosis and cats.

Authors:  Rita Espí Rito Santo; Catarina Salgado; Filipa Prata; Ana Mouzinho
Journal:  BMJ Case Rep       Date:  2017-08-24

Review 2.  Imaging of Horner syndrome in pediatrics: association with neuroblastoma.

Authors:  Hedieh Khalatbari; Gisele E Ishak
Journal:  Pediatr Radiol       Date:  2020-10-06

3.  Cervical artery dissection after sports - An analytical evaluation of 190 published cases.

Authors:  Ludwig Schlemm; Christian H Nolte; Stefan T Engelter; Matthias Endres; Martin Ebinger
Journal:  Eur Stroke J       Date:  2017-07-10

Review 4.  Ptosis in childhood: A clinical sign of several disorders: Case series reports and literature review.

Authors:  P Pavone; Sung Yoon Cho; A D Praticò; R Falsaperla; M Ruggieri; Dong-Kyu Jin
Journal:  Medicine (Baltimore)       Date:  2018-09       Impact factor: 1.817

  4 in total

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