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Neonatal venolymphatic malformation with spontaneous parotid duct rupture: first case report.

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dc.contributor.author Gamage, D.C.T.
dc.contributor.author Jayamanne, B.D.W.
dc.contributor.author Quasim, S.F.
dc.contributor.author Kailidis, K.
dc.contributor.author Olabi, A.
dc.date.accessioned 2022-07-27T04:29:51Z
dc.date.available 2022-07-27T04:29:51Z
dc.date.issued 2022
dc.identifier.citation Oxford Medical Case Reports.2022;(6):225-228 en_US
dc.identifier.issn 2053-8855
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/24951
dc.description In PUBMED, Not Indexed in MEDLINE. en_US
dc.description.abstract Disorders of salivary glands especially the parotid gland very rare among neonates and children other than cytomegaly and parotitis epidermica. Venolymphatic malformations are very rare in children. Such presentation around the parotid region yet to be reported. This case report describes a rare presentation of a neonatal venolymphatic malformation on the parotid duct. A 4-week-old termly delivered male infant referred to by a general practitioner bruising over the left buccal area for 1 day from non-consanguine healthy parents. On examination a bluish discoloration in the buccal mucosa over a firm mildly tender area without signs of inflammation was seen. Ultrasound examination of the lesion showed fluid and solid soft tissue suggestive of haematoma and magnetic resonance imaging scan confirmed the rupture of the parotid duct with venolymphatic malformation. The child has been referred to the vascular malformation clinic and plastic surgical clinic in a tertiary care hospital for follow-up. en_US
dc.language.iso en en_US
dc.publisher Published by Oxford University Press and JSCR Publishing Ltd en_US
dc.subject Neonatal venolymphatic en_US
dc.title Neonatal venolymphatic malformation with spontaneous parotid duct rupture: first case report. en_US
dc.type Case Report en_US


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