Acquired Port-Wine Stain (Fegeler Syndrome): A Report of 3 Cases

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Acquired Port-Wine Stain (Fegeler Syndrome): A Report of 3 Cases.

Capillary malformation is a condition included in the group of vascular malformations. It is one of the most common vascular abnormalities and can affect up to 0.3% of newborns. It presents clinically as a homogeneous erythematous macule with well-defined borders. It is typically unilateral and is usually present at birth. However, cases of acquired capillary malformation have been reported in ...

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Acquired Port-Wine stain: Report of two cases

Acquired port-wine stain is a rare vascular lesion that mimics a congenital port-wine stain clinically and histologically, but is acquired after birth. A survey on more than 60 reported cases in the literature reveals that most of these cases are idiopathic, but some of the cases developed after physical or mechanical trauma, hormonal changes, chronic sun exposure, and medications (OCP, i...

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Dermatological sequela of a car accident: acquired Port-wine stain (Fegeler syndrome).

To cite: NussbaumerOchsner Y, Spinas G. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2015210860 DESCRIPTION A 71-year-old man with long-standing type 2 diabetes mellitus was admitted for optimisation of glucose control. His antihyperglycemic medication comprised metformin, glimepiride and insulin glargine at bedtime. He also reported mildly impaired cognitive f...

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A Comparison of Acquired Port-wine Stain with Congenital Port-wine Stain Using an Image Analyzer.

BACKGROUND Recent reports have proposed that there were no differences between acquired port-wine stain (APWS) and congenital port-wine stain (CPWS) except the onset of disease. Pulsed dye laser (PDL) therapy is regarded as the treatment of choice in PWS. Although in some articles, APWS might have shown a better response to PDL than CPWS, this is still controversial. It has been assumed however...

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ژورنال

عنوان ژورنال: Actas Dermo-Sifiliográficas (English Edition)

سال: 2017

ISSN: 1578-2190

DOI: 10.1016/j.adengl.2017.10.013