Results 51 to 60 of about 21,965 (216)

Acquired port-wine stain in an adult male: First reported case from India with review of literature

open access: yesIndian Journal of Dermatology, 2015
Port-wine stains (PWSs) are congenital vascular lesions caused by progressive ectasia of blood vessels located in the vascular plexus of the dermis. Acquired PWSs develop later in life but are identical in morphology and histology to the congenital PWSs.
Shuchi Bansal   +3 more
doaj   +1 more source

Identification of a PORCN c.1093C>T (p.Arg365Trp) Variant in a 12‐Year‐Old Girl With Goltz–Gorlin Syndrome

open access: yesClinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT We report the first female case of Goltz–Gorlin syndrome with the PORCN c.1093C>T (p.Arg365Trp) variant, previously described only in a male with Klinefelter syndrome. This case expands the known phenotypic and genotypic spectrum of FDH.
Anna Bolzon   +5 more
wiley   +1 more source

A rare case of overlapping Sturge–Weber syndrome and Klippel–Trenaunay syndrome associated with bilateral refractory childhood glaucoma

open access: yesIndian Journal of Ophthalmology, 2017
A 6-year-old girl presented with blurred vision and was found to have elevated intraocular pressure (IOP) and glaucomatous optic disc damage in both eyes.
Manju R Pillai   +3 more
doaj   +1 more source

Barnes Hospital Bulletin [PDF]

open access: yes, 1983
https://digitalcommons.wustl.edu/bjc_barnes_bulletin/1213/thumbnail ...

core   +1 more source

Pregnancy tumor and facial port-wine stain: A case report

open access: yesJournal of Craniomaxillofacial Research, 2018
Pyogenic granuloma is a common tumor-like growth of the oral cavity that traditionally has been considered to be non-neoplastic in nature. The pyogenic granuloma is a smooth or lobulated mass that is usually pedunculated, although some lesions are ...
Mohsen Barzegar   +5 more
doaj  

Laser treatment of Port-wine stains [PDF]

open access: yes, 2001
A state-of-the-art pulsed dye laser machine to treat port-wine stains and other vascular lesions has been available in the Malta Health Service since 1999.
Boffa, Michael J.
core  

Cerebrovascular Malformations Associated With Hereditary Hemorrhagic Telangiectasia and HHT‐Like Syndromes: A Comparative Overview

open access: yesEuropean Journal of Neurology, Volume 33, Issue 2, February 2026.
Hereditary hemorrhagic telangiectasia (HHT) and several HHT‐like syndromes, including Wyburn–Mason, Cobb, Klippel–Trénaunay, Parkes Weber, neurofibromatosis type 1, PHACE(S), capillary malformation–AVM (CM‐AVM), Juvenile polyposis/HHT overlap, HHT type 5, PTEN hamartoma tumor syndrome, and blue rubber bleb nevus syndrome, share overlapping ...
Matteo Palermo, Carmelo Lucio Sturiale
wiley   +1 more source

Sturge Weber Syndrome: A Case Study [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2017
The aim of this case review was to touch upon the various clinical presentations and diagnostic features of Sturge-Weber syndrome (SWS) as seen in the dental/medical practice.
Mahesh Neerupakam   +3 more
doaj   +1 more source

Beyond Treatment: The Strategy of Nonintervention in Choroidal Hemangioma

open access: yesClinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT The circumscribed choroidal hemangioma (CCH) is a benign congenital eye tumor whose etiology is not clear. A 41‐year‐old female patient came with a 2‐year history of slowly progressive deteriorating vision in her right eye. In the left eye, the best‐corrected visual acuity (BCVA) was 6/6, and counting fingers at 1 m in the right eye.
Humdan Khan   +8 more
wiley   +1 more source

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