Diagnosis and Treatment of Oral Venous Malformation in a Child.
Journal
The Journal of craniofacial surgery
ISSN: 1536-3732
Titre abrégé: J Craniofac Surg
Pays: United States
ID NLM: 9010410
Informations de publication
Date de publication:
Jun 2020
Jun 2020
Historique:
pubmed:
14
4
2020
medline:
3
10
2020
entrez:
14
4
2020
Statut:
ppublish
Résumé
Venous malformations (VMs) are congenital disorders that constitute about 40% of all vascular anomalies. These lesions do not regress spontaneously and may increase in size during childhood. The case of a 10-year-old girl with an extensive oral VM is reported. Intraoral examination revealed the presence of purplish nodules in the alveolar mucosa and gingiva from anterior maxilla. Doppler ultrasound showed a well-defined hypoechoic image and increased vascularization with low blood flow for the alveolar mucosa lesion. The patient was submitted to intralesional injections of the ethanolamine oleate/mepivacaine sclerosing solution. After four sessions, there was a significant reduction of the lesions. However, the patient abandoned the treatment and the oral VM grew progressively. After 1 year, sclerotherapy was resumed and performed weekly. After 10 session of sclerotherapy, the oral VM totally regressed. The childhood is a critical period for oral VM growth. Doppler ultrasound and sclerotherapy can be effective for the management of extensive lesions in children.
Identifiants
pubmed: 32282473
doi: 10.1097/SCS.0000000000006363
pii: 00001665-202006000-00098
doi:
Substances chimiques
Oleic Acids
0
Sclerosing Solutions
0
Mepivacaine
B6E06QE59J
ethanolamine oleate
U4RY8MRX7C
Types de publication
Case Reports
Journal Article
Langues
eng
Pagination
e393-e394Références
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