نتایج جستجو برای: port wine stain
تعداد نتایج: 61519 فیلتر نتایج به سال:
We report a case of a 17-month-old child affected by Sturge-Weber syndrome who had unusually rapid overgrowth of the left frontal, temporal, orbital, and maxillary regions. CT angiography illustrated osteohypertrophy with periostitis and associated soft tissue hypertrophy directly corresponding to the distribution of the cutaneous port-wine stain. Extended maxillectomy was performed because of ...
Sturge Weber Syndrome or encephalo-trigeminal angiomatosis is non-hereditary, congenital and rare disorder of unknown aetiology. It is characterised by vascular malformation with capillary venous angiomas involving face, eye and leptomeninges resulting in neurological and orbital manifestations. A case of 23 years old female presented with history of tonic-clonic convulsions, evidence of Port w...
Port-wine stain (PWS) is one of the representative cutaneous vascular malformations. Pulse dye laser (PDL) a traditional treatment method to treat PWS. A newly developed potassium-titanyl-phosphate (KTP) laser, DermaV, can be irradiated with single pulse, or pulse divided into several sub-pulses in length 0.3ms 1.5ms. This study aimed investigate skin response KTP and PDL according different du...
Sturge –Weber syndrome (SWS) or encephalotrigeminal angiomatosis is a sporadic,congenital phakomatosis of unknown etiology.Diagnosed by the triad of facial port wine stain(PWS) in the trigeminal nerve distribution, leptomeningeal venous angiomatosis ,and glaucoma. Bilateral Sturge-Weber Syndrome is a rare entity. We present in this report a rare case of bilateral SWS type II , with PWS involvin...
Sir, Thorium X, a natural isotope of radium, was the main radiotherapeutic modality for treating vascular lesions of the skin including port-wine stain (PWS) available to dermatologists during the 1930s to 1950s. It disappeared from dermatological practice around the 1960s, and the chapter on thorium X was considered closed (1, 2). However, occasionally long-term sequelae have been described (2...
Klippel-Trenaunay syndrome (KTS) is a rare complex vascular with limb hypertrophy. KTS diagnosed if at least two of the three features capillary malformation, venous and soft tissue and/or bone overgrowth are present. Of these, malformation (i.e., port-wine stain) most commonly observed feature but may be absent in atypical KTS. We herein report case unilateral
Submit Manuscript | http://medcraveonline.com sometimes it may occur as an autosomal dominant trait [1,2]. Klippel-Trenaunay-Weber Syndrome is a cutaneous vascular malformation affecting the development of blood vessels, soft tissues and bones [3]. This is a non-heritable disorder which is present at birth and usually involves lower limb but may involve more than one limb and a portion of the t...
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