Abstract
The authors report a case of oro-facial port-wine stain angiomatosis with
cutaneous and mucosal lesions localized in the first and the second branch
surface distribution areas of the right trigeminal nerve in association with
right upper and lower lip, cheek, and hemimaxillary true hypertrophy leading to a
severe dento-skeletal malocclusion with openbite and facial asymmetry. The
authors through a revision of the Bibliography locate nosologically this case
among the rare congenital angiodysplastic syndromes affecting the maxillo-facial
district as the Sturge-Weber and the Klippel-Trenaunay syndromes. They debate
also about etiopathogenetic, clinical, differential diagnosis, and therapeutic
aspects concerning the treatment of patients affected by this kind of
malformation.
Lingua originale | English |
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pagine (da-a) | 485-489 |
Numero di pagine | 5 |
Rivista | THE JOURNAL OF CRANIOFACIAL SURGERY |
Volume | 12 |
DOI | |
Stato di pubblicazione | Pubblicato - 2001 |
Keywords
- Adult
- Humans
- Macroglossia
- Magnetic Resonance Imaging
- Male
- Malocclusion
- Sturge-Weber Syndrome