Results 1 to 10 of about 21,965 (216)

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

open access: yesCase 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   +2 more sources

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

open access: yesJournal 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   +3 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   +2 more sources

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

open access: yesAnais 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   +2 more sources

Truncal varicosities and bilateral port-wine stain with spinal deformities associated with Klippel–Trenaunay–Weber syndrome

open access: yesIndian Journal of Dermatology, 2020
Klippel–Trenaunay–Weber syndrome (KTWS) is a rare congenital disorder characterized by asymmetric limb hypertrophy, usually of the lower limbs, as well as vascular anomalies and capillary malformations under the skin, termed as port-wine stain.
Amr Abdelhamed   +3 more
doaj   +2 more sources

The Diagnosis and Treatment Technology of Port-Wine Stain, and the Prospect of Future Treatment [PDF]

open access: yesDermatology and Therapy
Port-wine stain (PWS) is a congenital capillary malformation with a 0.3–0.5% prevalence. This article reviews key techniques and advancements in the diagnosis and treatment of PWS.
Minghui Li, Yang Song, Junfeng Zhou
doaj   +2 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   +4 more sources

Laser treatment of port-wine stains

open access: yesClinical, Cosmetic and Investigational Dermatology, 2015
Lori A Brightman,1 Roy G Geronemus,1 Kavitha K Reddy2 1Laser and Skin Surgery Center of New York, New York, NY, USA; 2Department of Dermatology, Boston University School of Medicine, Boston, MA, USA Abstract: Port-wine stains are a type of capillary ...
Brightman LA, Geronemus RG, Reddy KK
doaj   +5 more sources

Non-invasive detection technology in port-wine stain treatment [PDF]

open access: yesChinese Medical Journal, 2022
Xue Wang   +9 more
doaj   +2 more sources

Port wine stains [PDF]

open access: yesJournal of the Royal Society of Medicine, 1987
To the Editor.— Smoller and Rosen 1 have shown morphological evidence of abnormal vascular innervation in the skin of patients with port-wine stains, and they have postulated that the progressive vascular dilatation in this condition is the result of impaired neural control.
G B, Colver, J A, Savin
  +6 more sources

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