Results 21 to 30 of about 21,947 (201)

The Klippel-Trenaunay syndrome (KTS): A case report in an infant

open access: yesJournal of Rawalpindi Medical College, 2020
Background: Klippel-Trenaunay syndrome (KTS) is a rare congenital disease having an incidence of 1/20-40,000, live births. KTS is a congenital, vascular disorder affecting usually one or rarely more than one limbs. It is characterized by port wine stain (
Muhammad Khalil Surani   +3 more
doaj   +1 more source

Optimum pulse duration and radiant exposure for vascular laser therapy of dark port-wine skin: a theoretical study [PDF]

open access: yes, 2003
Laser therapy for cutaneous hypervascular malformations such as port-wine stain birthmarks is currently not feasible for dark-skinned individuals. We study the effects of pulse duration, radiant exposure, and cryogen spray cooling (CSC) on the thermal ...
Anvari, Bahman   +2 more
core   +1 more source

Angiolymphoid Hyperplasia With Eosinophilia‐Acquired Port‐Wine‐Stain–Like Lesions: Attempt At Treatment With The Argon Laser [PDF]

open access: yes, 1988
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/110832/1/hed00011 ...
Elsenety, Evette N.   +2 more
core   +1 more source

Oral pyogenic granuloma in a port-wine stain: A rare co-occurrence

open access: yesSRM Journal of Research in Dental Sciences, 2017
Oral pyogenic granuloma is an inflammatory hyperplasia seen in the oral cavity occurring in response to stimuli such as local irritants and hormonal factors.
Medhini Madi   +3 more
doaj   +1 more source

Intracerebral hemorrhage in Sturge Weber Syndrome: A case report [PDF]

open access: yesRomanian Journal of Neurology
Background. Encephalotrigeminal angiomatosis also called Sturge Weber Syndrome (SWS) is neurocutaneous abnormality with angioma affecting the leptomeninges and the face skin, commonly in the eyes and maxillary distribution of trigeminal nerve.
Rizaldy Taslim Pinzon   +1 more
doaj   +1 more source

Combined lymphangioma and hemangioma of the spleen in a patient with Klippel–Trénaunay syndrome [PDF]

open access: yes, 2012
Introduction. Klippel–Trénaunay syndrome (KTS) is a very rare congenital anomaly of blood vessels, characterized by the following clinical triad: varicose superficial veins, port-wine stain and usually bony and soft tissue hypertophy of extremities ...
Azanjac Goran   +5 more
core   +1 more source

Vascular Malformation of the Face: a Rare Case with Follow-up of 18 Years

open access: yesActa Stomatologica Croatica, 2017
Objective: Vascular malformations are structural anomalies in the blood vessels. They are present at birth and persist throughout life. These malformations can be classified according to the type of vessel involved.
José Alcides Almeida de Arruda   +4 more
doaj   +1 more source

Bilateral Ocular and Facial with Unilateral Intracranial Involvement In Sturge Weber Syndrome: A Case Report and Review of Literature

open access: yesDelhi Journal of Ophthalmology, 2017
The Sturge-Weber syndrome (SWS) is a rare congenital disorder involving the eye in the form of glaucoma and choroidal hemangioma, facial skin in the form of port wine stain, usually in the distribution of ophthalmic division of the trigeminal nerve, and ...
Mihika Dube   +2 more
doaj   +1 more source

Acquired Port-Wine Stain: Not a simple stain! [PDF]

open access: yes, 2018
n/
A Abdelmaksoud, Michelangelo Vestita
core   +1 more source

Láser y luz pulsada intensa en el tratamiento de hemangiomas infantiles y malformaciones vasculares [PDF]

open access: yes, 2004
The use of the indications of the laser in treating vascular malformations and infantile haemangiomas is based on the theory of selective photothermolysis, in which the oxyhaemoglobin is the target chromophore on which the light of the laser acts ...
Mihm, M.C. (M.C.)   +2 more
core   +1 more source

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