Results 11 to 20 of about 21,947 (201)
A Rare Presentation of Acquired Port Wine Stain in an Elderly Male
Nepalese Medical Journal, 2021 Acquired port wine stain though an uncommon entity that develops later in life, resembles congenital port wine stain morphologically and histologically. Congenital port wine stains are vascular lesions caused by progressive ectasia of blood vessels which
Prasanna Kumar Jha +1 more
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Influence of Port-wine Stains on Quality of Life of Children and Their Parents
Acta Dermato-Venereologica, 2021 Port-wine stains are congenital vascular malformations that affect the quality of life of children and their parents. This study used the Family Dermatology Life Quality Index and Children’s Dermatology Life Quality Index to examine the effects of port ...
Fan Jiang +5 more
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Co-occurrence of tuberous sclerosis with port wine stain
Indian Journal of Paediatric Dermatology, 2021 Tuberous sclerosis complex is a rare autosomal dominant neurocutaneous disorder characterized by the presence of multiple tumors influencing diverse body frameworks including the central nervous system, skin, eyes, heart, lungs, kidney, and bones.
Rashmi Agarwal +3 more
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Indian Journal of Dermatology, 2015 Port wine stain and juvenile localized scleroderma are two different dermatoses usually encountered in pediatric age group. Up to now, there are reports of morphea patients initially diagnosed and treated as port wine stain.
Seval Dogruk Kacar +5 more
doaj +1 more source
Spectrum of CT and MR findings in Sturge-Weber syndrome: A case report
Medical Journal of Dr. D.Y. Patil University, 2014 Sturge-Weber syndrome is an uncommon, sporadically occurring neurocutaneous syndrome characterized by port wine stain (facial nevus flammeus), congenital glaucoma, and anomalous leptomeningeal angiomatous malformation.
Pallavi J Agrawal +3 more
doaj +1 more source
Characterization of Laser-Resistant Port Wine Stain Blood Vessels Using In Vivo Reflectance Confocal Microscopy. [PDF]
, 2019 Background and objectivesPort wine stain (PWS) is a congenital vascular malformation of the human skin. Laser is the treatment of choice for PWS. Laser-resistant PWS is one crucial factor accounting for inadequate treatment outcome, which needs to be ...
Chen, Jing +8 more
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Cutaneous New World Leishmaniasis on a Port-wine stain birthmark [PDF]
Anais Brasileiros de Dermatologia, 2014 We present an interesting case report of two sarcoid-like lesions on a port-wine stain (PWS) birthmark in a Brazilian patient which on investigation proved to be cutaneous leishmaniasis.
Paulo Ricardo Criado +3 more
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Ocular manifestations of Sturge–Weber syndrome: pathogenesis, diagnosis, and management [PDF]
, 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
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New vascular classification of port-wine stains: improving prediction of Sturge-Weber risk [PDF]
, 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
Primary intra osseous venous malformation of nasal bone: A rare case report
Indian 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