Results 41 to 50 of about 30,124 (290)

New vascular classification of port-wine stains: improving prediction of Sturge-Weber risk [PDF]

open access: yes, 2014
Background Facial port-wine stains (PWSs) are usually isolated findings; however, when associated with cerebral and ocular vascular malformations they form part of the classical triad of Sturge–Weber syndrome (SWS).
Aylett, SE   +5 more
core   +1 more source

Ocular manifestations of Sturge–Weber syndrome: pathogenesis, diagnosis, and management [PDF]

open access: yes, 2016
Sturge-Weber syndrome has been included in the group of phakomatoses that is characterized by hamartomas involving the brain, skin, and eyes. The characteristic facial port-wine stain, involving the first branch of the trigeminal nerve and the embryonic ...
Abdolrahimzadeh, Solmaz   +4 more
core   +1 more source

Primary intra osseous venous malformation of nasal bone: A rare case report

open access: yesIndian Journal of Plastic Surgery, 2014
Primary intra osseous venous malformation with involvement of nasal bone is a rare phenomenon. Nasal bone intraosseous venous malformation on a back ground of port wine stain of face has not been reported in the available literature.
Ajit Kumar Pati   +3 more
doaj   +1 more source

The Klippel-Trenaunay syndrome (KTS): A case report in an infant

open access: yesJournal of Rawalpindi Medical College, 2020
Background: Klippel-Trenaunay syndrome (KTS) is a rare congenital disease having an incidence of 1/20-40,000, live births. KTS is a congenital, vascular disorder affecting usually one or rarely more than one limbs. It is characterized by port wine stain (
Muhammad Khalil Surani   +3 more
doaj   +1 more source

Angiolymphoid Hyperplasia With Eosinophilia‐Acquired Port‐Wine‐Stain–Like Lesions: Attempt At Treatment With The Argon Laser [PDF]

open access: yes, 1988
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/110832/1/hed00011 ...
Elsenety, Evette N.   +2 more
core   +1 more source

Optimum pulse duration and radiant exposure for vascular laser therapy of dark port-wine skin: a theoretical study [PDF]

open access: yes, 2003
Laser therapy for cutaneous hypervascular malformations such as port-wine stain birthmarks is currently not feasible for dark-skinned individuals. We study the effects of pulse duration, radiant exposure, and cryogen spray cooling (CSC) on the thermal ...
Anvari, Bahman   +2 more
core   +1 more source

Combined lymphangioma and hemangioma of the spleen in a patient with Klippel–Trénaunay syndrome [PDF]

open access: yes, 2012
Introduction. Klippel–Trénaunay syndrome (KTS) is a very rare congenital anomaly of blood vessels, characterized by the following clinical triad: varicose superficial veins, port-wine stain and usually bony and soft tissue hypertophy of extremities ...
Azanjac Goran   +5 more
core   +1 more source

Intracerebral hemorrhage in Sturge Weber Syndrome: A case report [PDF]

open access: yesRomanian Journal of Neurology
Background. Encephalotrigeminal angiomatosis also called Sturge Weber Syndrome (SWS) is neurocutaneous abnormality with angioma affecting the leptomeninges and the face skin, commonly in the eyes and maxillary distribution of trigeminal nerve.
Rizaldy Taslim Pinzon   +1 more
doaj   +1 more source

Vascular Malformation of the Face: a Rare Case with Follow-up of 18 Years

open access: yesActa Stomatologica Croatica, 2017
Objective: Vascular malformations are structural anomalies in the blood vessels. They are present at birth and persist throughout life. These malformations can be classified according to the type of vessel involved.
José Alcides Almeida de Arruda   +4 more
doaj   +1 more source

Acquired Port-Wine Stain: Not a simple stain! [PDF]

open access: yes, 2018
n/
A Abdelmaksoud, Michelangelo Vestita
core   +1 more source

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