Report of a newborn with hemimegalencephaly in association with Klippel-Trenaunay-Weber syndrome
Klippel-Trenaunay-Weber syndrome (KTW) is a rare phacomatosis whose main characteristics are: cutaneous angiomas (vascular nevi), varicose veins (arteriovenous fistulae) and hemihypertrophy of bones and soft tissues. This is a case report of KTW syndrome which was diagnosed in the first days of life...
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Format: | Article |
Language: | English |
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Serbian Medical Society
2005-01-01
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Series: | Srpski Arhiv za Celokupno Lekarstvo |
Subjects: | |
Online Access: | http://www.doiserbia.nb.rs/img/doi/0370-8179/2005/0370-81790502062O.pdf |
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author | Obradović Slobodan Vuletić Biljana Stojković-Anđelković Anđelka Igrutinović Zoran |
author_facet | Obradović Slobodan Vuletić Biljana Stojković-Anđelković Anđelka Igrutinović Zoran |
author_sort | Obradović Slobodan |
collection | DOAJ |
description | Klippel-Trenaunay-Weber syndrome (KTW) is a rare phacomatosis whose main characteristics are: cutaneous angiomas (vascular nevi), varicose veins (arteriovenous fistulae) and hemihypertrophy of bones and soft tissues. This is a case report of KTW syndrome which was diagnosed in the first days of life on the basis of characteristic vascular nevi on the skin of the trunk and extremities in addition to hypertrophy of the left part of the body. Neuroradiologically verified hemimegalencephaly associated with temporal hemangioma represents a special particularity in our case. Measures of monitoring the child as well as stimulating and therapeutic actions were the issues of discussion. |
first_indexed | 2024-12-18T14:22:35Z |
format | Article |
id | doaj.art-868fbaf554f74f68a7efd9e92857f3d1 |
institution | Directory Open Access Journal |
issn | 0370-8179 |
language | English |
last_indexed | 2024-12-18T14:22:35Z |
publishDate | 2005-01-01 |
publisher | Serbian Medical Society |
record_format | Article |
series | Srpski Arhiv za Celokupno Lekarstvo |
spelling | doaj.art-868fbaf554f74f68a7efd9e92857f3d12022-12-21T21:04:49ZengSerbian Medical SocietySrpski Arhiv za Celokupno Lekarstvo0370-81792005-01-011331-2626410.2298/SARH0502062OReport of a newborn with hemimegalencephaly in association with Klippel-Trenaunay-Weber syndromeObradović SlobodanVuletić BiljanaStojković-Anđelković AnđelkaIgrutinović ZoranKlippel-Trenaunay-Weber syndrome (KTW) is a rare phacomatosis whose main characteristics are: cutaneous angiomas (vascular nevi), varicose veins (arteriovenous fistulae) and hemihypertrophy of bones and soft tissues. This is a case report of KTW syndrome which was diagnosed in the first days of life on the basis of characteristic vascular nevi on the skin of the trunk and extremities in addition to hypertrophy of the left part of the body. Neuroradiologically verified hemimegalencephaly associated with temporal hemangioma represents a special particularity in our case. Measures of monitoring the child as well as stimulating and therapeutic actions were the issues of discussion.http://www.doiserbia.nb.rs/img/doi/0370-8179/2005/0370-81790502062O.pdfKlippel-Trenaunay-Weber syndromehemimegalencephaly |
spellingShingle | Obradović Slobodan Vuletić Biljana Stojković-Anđelković Anđelka Igrutinović Zoran Report of a newborn with hemimegalencephaly in association with Klippel-Trenaunay-Weber syndrome Srpski Arhiv za Celokupno Lekarstvo Klippel-Trenaunay-Weber syndrome hemimegalencephaly |
title | Report of a newborn with hemimegalencephaly in association with Klippel-Trenaunay-Weber syndrome |
title_full | Report of a newborn with hemimegalencephaly in association with Klippel-Trenaunay-Weber syndrome |
title_fullStr | Report of a newborn with hemimegalencephaly in association with Klippel-Trenaunay-Weber syndrome |
title_full_unstemmed | Report of a newborn with hemimegalencephaly in association with Klippel-Trenaunay-Weber syndrome |
title_short | Report of a newborn with hemimegalencephaly in association with Klippel-Trenaunay-Weber syndrome |
title_sort | report of a newborn with hemimegalencephaly in association with klippel trenaunay weber syndrome |
topic | Klippel-Trenaunay-Weber syndrome hemimegalencephaly |
url | http://www.doiserbia.nb.rs/img/doi/0370-8179/2005/0370-81790502062O.pdf |
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