Sturge-Weber Syndrome Complicating with Ipsilateral
Hemangioma-liked Nasal Polyps
Liu Yiwei, Sun Ke and Tang Jianguo*
DOI: 10.26717/BJSTR.2017.01.000311
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- General Surgery Consultant, France
Corresponding author:
Tang Jianguo, Department of Otolaryngology-Head and Neck Surgery, Sir Run Run Shaw Hospital, Medical College of Zhejiang
University, Hangzhou, 310016, China
Received: August 14, 2017; Published: August 30, 2017
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Abstract
Sturge-Weber syndrome (SWS), also known as
encephalotrigeminal angiomatosis, was reported by Schirmer,
Sturge and Weber in succession in mid-19th century. And it is a
neurocutaneous disease classically presenting with a facial portwine
stain in the ophthalmic distribution of the trigeminal nerve,
glaucoma and vascular eye abnormalities, and an ipsilateral
occipital leptomeningeal angioma. It is possible to observe nose
and sinus involvement in SWS [1].
|Sturge-Weber Syndrome Complicating with Ipsilateral
Hemangioma-liked Nasal Polyps|
|Report of a Case|
Comment|
Conclusion|
|References|
ISSN: 2574 -1241
