Results 1 to 10 of about 30,124 (290)

Hemoporfin-mediated photodynamic therapy for the treatment of port-wine stain birthmarks in pediatric patients [PDF]

open access: goldAnais Brasileiros de Dermatologia, 2017
: Port-wine stain is a type of common congenital superficial telangiectasia in the dermal layer mostly occurring on the forehead, face, and neck. The affected skin shows abnormal red or purple lesions, which darken and thicken.
Yunjie Zhang   +3 more
doaj   +4 more sources

Sturge–Weber Syndrome with Bilateral Port-Wine Stain [PDF]

open access: goldCase Reports in Pediatrics, 2022
Sturge–Weber syndrome is a rare congenital neurocutaneous disorder characterized by dermatological, ophthalmological, and neurological manifestations. It occurs due to abnormal persistence of embryonic vascular plexus.
Bishnu Deep Pathak   +5 more
doaj   +4 more sources

Hematoporphyrin Monomethyl Ether Photodynamic Therapy of Port Wine Stain: Narrative Review [PDF]

open access: yesClinical, Cosmetic and Investigational Dermatology, 2023
Ping Diao, Chenglong Han, Xiaoxue Li, Yi Yang, Xian Jiang Department of Dermatology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, People’s Republic of ChinaCorrespondence: Xian Jiang, Email jennyxianj@163.comAbstract: Port wine ...
Diao P, Han C, Li X, Yang Y, Jiang X
doaj   +3 more sources

Societal-Perceived Health Utility of Hypertrophic Facial Port-Wine Stain and Laser Treatment. [PDF]

open access: hybridFacial Plast Surg Aesthet Med, 2020
Background: Port-wine stain (PWS) is a congenital capillary malformation occurring commonly in the head and neck. Left untreated, affected areas may darken and hypertrophy over time, resulting in pronounced disfigurement, risk of spontaneous hemorrhage ...
Heiser A   +4 more
europepmc   +4 more sources

Anatomical Evaluation for Successful Dye Laser Treatment of Port Wine Stain in Vietnamese Patients. [PDF]

open access: yesOpen Access Maced J Med Sci, 2019
AIM: To assess the efficacy in the treatment of port wine stain in the head and neck by using (Vbeam perfecta®). METHODS: Forty-two port wine stain patients were recruited at the National Hospital of Dermatology and Venereology, Hanoi, Vietnam. RESULTS:
Cao KP   +13 more
europepmc   +5 more sources

The Pathogenesis of Port Wine Stain and Sturge Weber Syndrome: Complex Interactions between Genetic Alterations and Aberrant MAPK and PI3K Activation [PDF]

open access: yesInternational Journal of Molecular Sciences, 2019
Port wine stain (PWS) is a congenital vascular malformation involving human skin. Approximately 15–20% of children a facial PWS involving the ophthalmic (V1) trigeminal dermatome are at risk for Sturge Weber syndrome (SWS), a neurocutaneous disorder with
, Martin C Mihm Jr, Wenbin Tan
exaly   +3 more sources

Pyogenic Granuloma in a Patient of Sturge-Weber Syndrome with Bilateral Port Wine Stain- A Rare Case Report [PDF]

open access: greenJournal of Krishna Institute of Medical Sciences University, 2014
Sturge-Weber syndrome (SWS) also known as encephalotrigeminal angiomatosis. It is a neurocutaneous syndrome, characterized by a facial vascular birthmark and neurological abnormalities.
Shantala Arunkumar   +3 more
doaj   +4 more sources

Outcome with topical sirolimus for port wine stain malformations after unsatisfactory results with pulse dye laser treatment alone. [PDF]

open access: diamondAnn Saudi Med, 2018
We used a topical formulation of sirolimus for treating port wine stain (PWS). Although pulsed dye laser (PDL) is the current treatment of choice for PWS, fast neovascularization after treatment is a major drawback.
Musalem HM   +3 more
europepmc   +4 more sources

Concurrent Occurrence of Lobular Capillary Haemangioma and Port-Wine Stain: A Case Report and Literature Review. [PDF]

open access: yesCureus, 2023
A port-wine stain is a type of non-neoplastic hamartomatous malformation of capillary blood vessels, resulting from ectatic capillaries present from birth.
Priya S   +4 more
europepmc   +2 more sources

Klippel-Trenaunay Syndrome With Atypical Presentation of Small Port-Wine Stain. [PDF]

open access: yesCureus, 2022
Klippel-Trenaunay Syndrome (KTS) is a rare congenital capillary/venous malformation (CVM) disorder associated with deep soft-tissue swelling. A seven-year-old Caucasian male with a history of Klippel-Trenaunay Syndrome presented to the dermatology clinic
Alazawi S, Wright K.
europepmc   +2 more sources

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