INVERSE KLIPPEL-TRENAUNAY SYNDROME
ABSTRACT Objective: To report a rare case of inverse Kipplel-Trenaunay. Case description: A 16-year-old girl with a grayish-depressed plaque on her left thigh. Angioresonance showed a vascular malformation affecting the skin and subcutaneous tissue. Comments: Inverse Klippel-Trenaunay is a Klippel-Trenaunay syndrome variation in which there are capillary and venous malformations associated to hypotrophy or shortening of the affected limb. Modifications on the limb’s length or width result from alterations in bones, muscles, or subcutaneous tissues. It has few described cases. Further clinical and molecular studies must be performed for a proper understanding.
Main Authors: | , |
---|---|
Format: | Digital revista |
Language: | English |
Published: |
Sociedade de Pediatria de São Paulo
2020
|
Online Access: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822020000100612 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
id |
oai:scielo:S0103-05822020000100612 |
---|---|
record_format |
ojs |
spelling |
oai:scielo:S0103-058220200001006122020-12-15INVERSE KLIPPEL-TRENAUNAY SYNDROMESantino,Mariana Franco FerrazLopes,Maria João Paiva Skin abnormalities Vascular diseases Subcutaneous tissue Klippel-Trenaunay-Weber syndrome ABSTRACT Objective: To report a rare case of inverse Kipplel-Trenaunay. Case description: A 16-year-old girl with a grayish-depressed plaque on her left thigh. Angioresonance showed a vascular malformation affecting the skin and subcutaneous tissue. Comments: Inverse Klippel-Trenaunay is a Klippel-Trenaunay syndrome variation in which there are capillary and venous malformations associated to hypotrophy or shortening of the affected limb. Modifications on the limb’s length or width result from alterations in bones, muscles, or subcutaneous tissues. It has few described cases. Further clinical and molecular studies must be performed for a proper understanding.info:eu-repo/semantics/openAccessSociedade de Pediatria de São PauloRevista Paulista de Pediatria v.38 20202020-01-01info:eu-repo/semantics/reporttext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822020000100612en10.1590/1984-0462/2020/38/2020091 |
institution |
SCIELO |
collection |
OJS |
country |
Brasil |
countrycode |
BR |
component |
Revista |
access |
En linea |
databasecode |
rev-scielo-br |
tag |
revista |
region |
America del Sur |
libraryname |
SciELO |
language |
English |
format |
Digital |
author |
Santino,Mariana Franco Ferraz Lopes,Maria João Paiva |
spellingShingle |
Santino,Mariana Franco Ferraz Lopes,Maria João Paiva INVERSE KLIPPEL-TRENAUNAY SYNDROME |
author_facet |
Santino,Mariana Franco Ferraz Lopes,Maria João Paiva |
author_sort |
Santino,Mariana Franco Ferraz |
title |
INVERSE KLIPPEL-TRENAUNAY SYNDROME |
title_short |
INVERSE KLIPPEL-TRENAUNAY SYNDROME |
title_full |
INVERSE KLIPPEL-TRENAUNAY SYNDROME |
title_fullStr |
INVERSE KLIPPEL-TRENAUNAY SYNDROME |
title_full_unstemmed |
INVERSE KLIPPEL-TRENAUNAY SYNDROME |
title_sort |
inverse klippel-trenaunay syndrome |
description |
ABSTRACT Objective: To report a rare case of inverse Kipplel-Trenaunay. Case description: A 16-year-old girl with a grayish-depressed plaque on her left thigh. Angioresonance showed a vascular malformation affecting the skin and subcutaneous tissue. Comments: Inverse Klippel-Trenaunay is a Klippel-Trenaunay syndrome variation in which there are capillary and venous malformations associated to hypotrophy or shortening of the affected limb. Modifications on the limb’s length or width result from alterations in bones, muscles, or subcutaneous tissues. It has few described cases. Further clinical and molecular studies must be performed for a proper understanding. |
publisher |
Sociedade de Pediatria de São Paulo |
publishDate |
2020 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822020000100612 |
work_keys_str_mv |
AT santinomarianafrancoferraz inverseklippeltrenaunaysyndrome AT lopesmariajoaopaiva inverseklippeltrenaunaysyndrome |
_version_ |
1756401308113305600 |