نتایج جستجو برای: port wine stains

تعداد نتایج: 51497  

2017
Linda Kundzina Sandra Lejniece

BACKGROUND Klippel-Trenaunay-Weber syndrome is a rare syndrome; unfortunately, very few studies of the connection between hypersplenism, nephrotic syndrome, and Klippel-Trenaunay-Weber syndrome have been published. CASE PRESENTATION We report the case of a 40-year-old white man with a typical clinical presentation of Klippel-Trenaunay-Weber syndrome, including "port-wine stains," varicose vei...

Journal: :Optics express 2005
Michal Heger Johan Beek Karin Stenback Dirk Faber Martin van Gemert Can Ince

Due to the limited number of suitable intravital microscopy techniques, relatively little is known about the opto-thermal (endo)vascular responses to selective photothermolysis, used as a default treatment modality for superficial vascular anomalies such as port wine stains, telangiectasias, and hemangiomas. In this preliminary study we present a novel microscopy technique for studying (endo)va...

Journal: :Archives of dermatology 2012
Rachael L Moore Virginie de Schaetzen Marissa Joseph Ivy Ann Lee Yvette Miller-Monthrope B Ryan Phelps Shimane S Lekalake Sarah J Ratcliffe Harrison Nguyen Qin He Peter Rady Stephen Tyring Carrie L Kovarik

1. Ohlerth S, Laluhová D, Buchholz J, Roos M, Walt H, Kaser-Hotz B. Changes in vascularityandbloodvolumeasa resultofphotodynamic therapycanbeassessed with power Doppler ultrasonography. Lasers Surg Med. 2006;38(3):229-234. 2. Li W, Yamada I, Masumoto K, Ueda Y, Hashimoto K. Photodynamic therapy with intradermal administration of 5-aminolevulinic acid for port-wine stains. J Dermatolog Treat. 20...

2011
Hee Sun Chang Young-Gull Kim June Hyunkyung Lee

Port wine stains (PWS) are congenital capillary malformations consisting of ectasia of capillaries and venules. At birth,lesions are flat and relatively uniform in color, but evolve with age to become raised, thickened, irregularly surfaced, and deeply colored. Therefore, it is considered optimal to begin treatment of patients at an early age. Conventional treatment modalities, such as electroc...

Journal: :Facial plastic surgery : FPS 2012
Arisa E Ortiz J Stuart Nelson

BACKGROUND AND OBJECTIVES Port-wine stains (PWSs) are capillary vascular malformations that are commonly resistant to treatment. Currently, the pulsed dye laser (PDL) is the treatment of choice. Multiple treatments are required and complete blanching after laser irradiation is rarely achieved. We review current therapeutic modalities for PWSs and recent developments for enhanced clearance. ST...

2014
Valentina Tono Sara Bertoletti Francesca Maltese Francesco Canonico Erik Sganzerla Carlo Giussani Maria Luisa Melzi Andrea Biondi

Congenital dermal sinuses are a rare entity of spinal dysraphism. Most patients have cutaneous markers of their presence, including nevus or port wine stains, dimple, hypertrichosis and subcutaneous lipoma. Inclusion tumors, such as dermoid tumor, are associated to dermal sinus tract; they are congenital, benign and slow-growing lesions of midline. Their clinical relevance is due to the possibi...

Journal: :Physics in medicine and biology 1997
M J van Gemert J S Nelson T E Milner D J Smithies W Verkruysse J F de Boer G W Lucassen D M Goodman B S Tanenbaum L T Norvang L O Svaasand

The treatment of port wine stains (PWSs) using a flashlamp-pumped pulsed dye laser is often performed using virtually identical irradiation parameters. Although encouraging clinical results have been reported, we propose that lasers will only reach their full potential provided treatment parameters match individual PWS anatomy and physiology. The purpose of this paper is to review the progress ...

2014
Dilek Sarici Mustafa Ali Akin Selim Kurtoglu Filiz Tubas Serdar Umit Sarici

Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE) syndrome is a recently delineated disorder that comprises vascular malformations (typically truncal), dysregulated adipose tissue, scoliosis, enlarged bony structures (typically of the legs) without progression, or distorting bony overgrowth. The name CLOVE was subsequently extended to CLOVES to emphasize the a...

2011
Arun Joshi Yashpal Manchanda Manish Rijhwani

The association of a vascular lesion with melanocytic nevi was first described by Ota et, al in 1947, and given the name phakomatosis pigmentovascularis(PPV). Later on this term was used for the cases with simultaneous occurrence of congenital vascular and pigmented (epidermal or melanocytic) anomalies. Our first case is a 12-year-old Kuwaiti boy who had extensive port-wine stain (nevus flammeu...

2015
Andrew Rockafellow Whitney Florin Elizabeth Philipone David Koslovsky

Pyogenic granuloma is a type of inflammatory hyperplasia often seen in the oral cavity and occurs in response to stimuli such as local irritants and hormonal factors. Pyogenic granulomas associated with pregnancy are referred to as pregnancy tumors. This report describes the presentation and surgical management of a large pregnancy tumor occurring in a patient with an overlying isolated facial ...

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