Encephalotrigeminal Angiomatosis with Facial Lobular Capillary Hemangioma: An Unusual Case Report

Encephalotrigeminal angiomatosis, also called Sturge–Weber syndrome (SWS), is a syndrome of etiology which is not yet clear. It is a nonhereditary condition. The clinical features include pigmentation over the facial skin known as port-wine stain, abnormalities of ocular region, and central nervous...

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Autores principales: Karagir, Amol, Adaki, Shridevi, Magdum, Dilip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025953/
https://www.ncbi.nlm.nih.gov/pubmed/33842296
http://dx.doi.org/10.4103/ijabmr.IJABMR_301_19
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author Karagir, Amol
Adaki, Shridevi
Magdum, Dilip
author_facet Karagir, Amol
Adaki, Shridevi
Magdum, Dilip
author_sort Karagir, Amol
collection PubMed
description Encephalotrigeminal angiomatosis, also called Sturge–Weber syndrome (SWS), is a syndrome of etiology which is not yet clear. It is a nonhereditary condition. The clinical features include pigmentation over the facial skin known as port-wine stain, abnormalities of ocular region, and central nervous system involvement as leptomeningeal angioma. In this manuscript, we present a rare case report with an unusual combination of SWS with facial lobular capillary hemangioma.
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spelling pubmed-80259532021-04-08 Encephalotrigeminal Angiomatosis with Facial Lobular Capillary Hemangioma: An Unusual Case Report Karagir, Amol Adaki, Shridevi Magdum, Dilip Int J Appl Basic Med Res Case Report Encephalotrigeminal angiomatosis, also called Sturge–Weber syndrome (SWS), is a syndrome of etiology which is not yet clear. It is a nonhereditary condition. The clinical features include pigmentation over the facial skin known as port-wine stain, abnormalities of ocular region, and central nervous system involvement as leptomeningeal angioma. In this manuscript, we present a rare case report with an unusual combination of SWS with facial lobular capillary hemangioma. Wolters Kluwer - Medknow 2021 2021-01-26 /pmc/articles/PMC8025953/ /pubmed/33842296 http://dx.doi.org/10.4103/ijabmr.IJABMR_301_19 Text en Copyright: © 2021 International Journal of Applied and Basic Medical Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Karagir, Amol
Adaki, Shridevi
Magdum, Dilip
Encephalotrigeminal Angiomatosis with Facial Lobular Capillary Hemangioma: An Unusual Case Report
title Encephalotrigeminal Angiomatosis with Facial Lobular Capillary Hemangioma: An Unusual Case Report
title_full Encephalotrigeminal Angiomatosis with Facial Lobular Capillary Hemangioma: An Unusual Case Report
title_fullStr Encephalotrigeminal Angiomatosis with Facial Lobular Capillary Hemangioma: An Unusual Case Report
title_full_unstemmed Encephalotrigeminal Angiomatosis with Facial Lobular Capillary Hemangioma: An Unusual Case Report
title_short Encephalotrigeminal Angiomatosis with Facial Lobular Capillary Hemangioma: An Unusual Case Report
title_sort encephalotrigeminal angiomatosis with facial lobular capillary hemangioma: an unusual case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025953/
https://www.ncbi.nlm.nih.gov/pubmed/33842296
http://dx.doi.org/10.4103/ijabmr.IJABMR_301_19
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AT magdumdilip encephalotrigeminalangiomatosiswithfaciallobularcapillaryhemangiomaanunusualcasereport

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