Literature DB >> 19194612

[Ramsay Hunt syndrome in children: four cases and review].

Carmen Sandoval C1, Alicia Núñez F, Macarena Lizama C, Cynthia Margarit S, Katia Abarca V, Raúl Escobar H.   

Abstract

Ramsay-Hunt Syndrome (RHS) is a rare affection characterized by peripheral facial paralysis (PFP), skin eruption in the auricular canal and cochleovestibular symptoms. It is produced by varicella-zoster virus (VZV) reactivation at the geniculate ganglia. We report four patients between 3 and 17 years-old with RHS. Earache was the first symptom in two cases and three had cochleovestibular compromise. The direct immunofluorescence from the vesicular lesion was positive for VZV in two of them. All patients received treatment with aeyelovir and in three cases, this was associated with steroids. Three children had complete resolution of the PFP. RHS is an infrequent disease in the pediatric population and it should be suspected in children with PFP, erythema, vesicles and/or auricular pain. Early treatment with aeyelovir therapy could improve the recovery rate of facial nerve palsy.

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Year:  2009        PMID: 19194612     DOI: /S0716-10182008000600009

Source DB:  PubMed          Journal:  Rev Chilena Infectol        ISSN: 0716-1018            Impact factor:   0.520


  2 in total

1.  Management of ramsay hunt syndrome in an acute palliative care setting.

Authors:  Shrenik Ostwal; Naveen Salins; Jayita Deodhar; Mary Ann Muckaden
Journal:  Indian J Palliat Care       Date:  2015 Jan-Apr

2.  Ramsay Hunt syndrome following otoplasty.

Authors:  Marco Antônio Rios Lima; Jacinto de Negreiros Júnior
Journal:  Braz J Otorhinolaryngol       Date:  2011 Nov-Dec
  2 in total

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