Frey syndrome in neurofibromatosis 1.

Ibrahim, Laila Farah; Brenner, Clare; McMenamin, Joe; Webb, David

Ibrahim, Laila Farah; Brenner, Clare; McMenamin, Joe; Webb, David.

Afiliación

Ibrahim LF; Department of Neonatology, Cork University Maternity Hospital, Cork, Ireland.

BMJ Case Rep ; 20112011 Mar 15.

Article en En | MEDLINE | ID: mdl-22698902

RESUMEN

A healthy 18-month-old girl presented with a history of intermittent hemifacial flushing when eating. Her symptom seemed to be exclusively triggered by chewing. Examination revealed cutaneous features of neurofibromatosis type 1 (NF1) and mild facial asymmetry. Imaging confirmed cerebral vacuolisation changes seen in NF1 and a left facial plexiform neurofibroma involving the parotid gland. This is the first reported case of Frey syndrome complicating NF1.

Asunto(s)

Neurofibroma Plexiforme/diagnóstico; Neurofibromatosis 1/diagnóstico; Neoplasias de la Parótida/diagnóstico; Sudoración Gustativa/etiología; Femenino; Humanos; Lactante; Neurofibroma Plexiforme/complicaciones; Neurofibromatosis 1/complicaciones; Neoplasias de la Parótida/complicaciones

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sudoración Gustativa / Neoplasias de la Parótida / Neurofibromatosis 1 / Neurofibroma Plexiforme Límite: Female / Humans / Infant Idioma: En Revista: BMJ Case Rep Año: 2011 Tipo del documento: Article País de afiliación: Irlanda Pais de publicación: Reino Unido

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