Limb hyperplasia: case report of an unusual variant of Klippel-Trenaunay syndrome and review of the literature.
Identifieur interne : 003472 ( Ncbi/Checkpoint ); précédent : 003471; suivant : 003473Limb hyperplasia: case report of an unusual variant of Klippel-Trenaunay syndrome and review of the literature.
Auteurs : Julie K. Gober-Wilcox [États-Unis] ; David L. Gardner ; Nancy E. Joste ; Carol L. Clericuzio ; Barrett ZlotoffSource :
- Cutis [ 0011-4162 ] ; 2009.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Syndrome de Klippel-Trénaunay.
- diagnostic : Syndrome de Klippel-Trénaunay.
- génétique : Syndrome de Klippel-Trénaunay.
- Enfant, Femelle, Humains.
English descriptors
- KwdEn :
- MESH :
- diagnosis : Klippel-Trenaunay-Weber Syndrome.
- genetics : Klippel-Trenaunay-Weber Syndrome.
- pathology : Klippel-Trenaunay-Weber Syndrome.
- Child, Female, Humans.
Abstract
Klippel-Trenaunay syndrome (KTS) is a rare disorder involving a triad of cutaneous capillary malformations (port-wine stain), varicose veins or venous malformations, and bony or soft tissue hyperplasia of an extremity. It is one of many heterogeneous disorders known as overgrowth syndromes that are characterized by either generalized or localized somatic overgrowth. Overgrowth syndromes each have unique clinical, behavioral, and genetic features, but some of these features overlap, causing diagnostic difficulty. Cutaneous manifestations, however, can be key to distinguishing the various syndromes. We present a patient with an unusual variant of KTS consisting of right upper extremity hyperplasia, lymphedema, and cutaneous and visceral lymphangiomas. We review several closely related syndromes and discuss the differential diagnosis of limb hyperplasia.
PubMed: 19537283
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 002E28
- to stream PubMed, to step Curation: 002E28
- to stream PubMed, to step Checkpoint: 002E28
- to stream Ncbi, to step Merge: 003472
- to stream Ncbi, to step Curation: 003472
Links to Exploration step
pubmed:19537283Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Limb hyperplasia: case report of an unusual variant of Klippel-Trenaunay syndrome and review of the literature.</title><author><name sortKey="Gober Wilcox, Julie K" sort="Gober Wilcox, Julie K" uniqKey="Gober Wilcox J" first="Julie K" last="Gober-Wilcox">Julie K. Gober-Wilcox</name><affiliation wicri:level="2"><nlm:affiliation>Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131-0001, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131-0001</wicri:regionArea><placeName><region type="state">Nouveau-Mexique</region></placeName></affiliation></author><author><name sortKey="Gardner, David L" sort="Gardner, David L" uniqKey="Gardner D" first="David L" last="Gardner">David L. Gardner</name></author><author><name sortKey="Joste, Nancy E" sort="Joste, Nancy E" uniqKey="Joste N" first="Nancy E" last="Joste">Nancy E. Joste</name></author><author><name sortKey="Clericuzio, Carol L" sort="Clericuzio, Carol L" uniqKey="Clericuzio C" first="Carol L" last="Clericuzio">Carol L. Clericuzio</name></author><author><name sortKey="Zlotoff, Barrett" sort="Zlotoff, Barrett" uniqKey="Zlotoff B" first="Barrett" last="Zlotoff">Barrett Zlotoff</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2009">2009</date><idno type="RBID">pubmed:19537283</idno><idno type="pmid">19537283</idno><idno type="wicri:Area/PubMed/Corpus">002E28</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">002E28</idno><idno type="wicri:Area/PubMed/Curation">002E28</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">002E28</idno><idno type="wicri:Area/PubMed/Checkpoint">002E28</idno><idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">002E28</idno><idno type="wicri:Area/Ncbi/Merge">003472</idno><idno type="wicri:Area/Ncbi/Curation">003472</idno><idno type="wicri:Area/Ncbi/Checkpoint">003472</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Limb hyperplasia: case report of an unusual variant of Klippel-Trenaunay syndrome and review of the literature.</title><author><name sortKey="Gober Wilcox, Julie K" sort="Gober Wilcox, Julie K" uniqKey="Gober Wilcox J" first="Julie K" last="Gober-Wilcox">Julie K. Gober-Wilcox</name><affiliation wicri:level="2"><nlm:affiliation>Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131-0001, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131-0001</wicri:regionArea><placeName><region type="state">Nouveau-Mexique</region></placeName></affiliation></author><author><name sortKey="Gardner, David L" sort="Gardner, David L" uniqKey="Gardner D" first="David L" last="Gardner">David L. Gardner</name></author><author><name sortKey="Joste, Nancy E" sort="Joste, Nancy E" uniqKey="Joste N" first="Nancy E" last="Joste">Nancy E. Joste</name></author><author><name sortKey="Clericuzio, Carol L" sort="Clericuzio, Carol L" uniqKey="Clericuzio C" first="Carol L" last="Clericuzio">Carol L. Clericuzio</name></author><author><name sortKey="Zlotoff, Barrett" sort="Zlotoff, Barrett" uniqKey="Zlotoff B" first="Barrett" last="Zlotoff">Barrett Zlotoff</name></author></analytic><series><title level="j">Cutis</title><idno type="ISSN">0011-4162</idno><imprint><date when="2009" type="published">2009</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Child</term><term>Female</term><term>Humans</term><term>Klippel-Trenaunay-Weber Syndrome (diagnosis)</term><term>Klippel-Trenaunay-Weber Syndrome (genetics)</term><term>Klippel-Trenaunay-Weber Syndrome (pathology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Enfant</term><term>Femelle</term><term>Humains</term><term>Syndrome de Klippel-Trénaunay (anatomopathologie)</term><term>Syndrome de Klippel-Trénaunay (diagnostic)</term><term>Syndrome de Klippel-Trénaunay (génétique)</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Syndrome de Klippel-Trénaunay</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Klippel-Trenaunay-Weber Syndrome</term></keywords><keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Syndrome de Klippel-Trénaunay</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Klippel-Trenaunay-Weber Syndrome</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Syndrome de Klippel-Trénaunay</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Klippel-Trenaunay-Weber Syndrome</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Child</term><term>Female</term><term>Humans</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Enfant</term><term>Femelle</term><term>Humains</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Klippel-Trenaunay syndrome (KTS) is a rare disorder involving a triad of cutaneous capillary malformations (port-wine stain), varicose veins or venous malformations, and bony or soft tissue hyperplasia of an extremity. It is one of many heterogeneous disorders known as overgrowth syndromes that are characterized by either generalized or localized somatic overgrowth. Overgrowth syndromes each have unique clinical, behavioral, and genetic features, but some of these features overlap, causing diagnostic difficulty. Cutaneous manifestations, however, can be key to distinguishing the various syndromes. We present a patient with an unusual variant of KTS consisting of right upper extremity hyperplasia, lymphedema, and cutaneous and visceral lymphangiomas. We review several closely related syndromes and discuss the differential diagnosis of limb hyperplasia.</div></front></TEI><affiliations><list><country><li>États-Unis</li></country><region><li>Nouveau-Mexique</li></region></list><tree><noCountry><name sortKey="Clericuzio, Carol L" sort="Clericuzio, Carol L" uniqKey="Clericuzio C" first="Carol L" last="Clericuzio">Carol L. Clericuzio</name><name sortKey="Gardner, David L" sort="Gardner, David L" uniqKey="Gardner D" first="David L" last="Gardner">David L. Gardner</name><name sortKey="Joste, Nancy E" sort="Joste, Nancy E" uniqKey="Joste N" first="Nancy E" last="Joste">Nancy E. Joste</name><name sortKey="Zlotoff, Barrett" sort="Zlotoff, Barrett" uniqKey="Zlotoff B" first="Barrett" last="Zlotoff">Barrett Zlotoff</name></noCountry><country name="États-Unis"><region name="Nouveau-Mexique"><name sortKey="Gober Wilcox, Julie K" sort="Gober Wilcox, Julie K" uniqKey="Gober Wilcox J" first="Julie K" last="Gober-Wilcox">Julie K. Gober-Wilcox</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Ncbi/Checkpoint
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003472 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Ncbi/Checkpoint/biblio.hfd -nk 003472 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Sante
|area= LymphedemaV1
|flux= Ncbi
|étape= Checkpoint
|type= RBID
|clé= pubmed:19537283
|texte= Limb hyperplasia: case report of an unusual variant of Klippel-Trenaunay syndrome and review of the literature.
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Checkpoint/RBID.i -Sk "pubmed:19537283" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Ncbi/Checkpoint/biblio.hfd \
| NlmPubMed2Wicri -a LymphedemaV1
| This area was generated with Dilib version V0.6.31. |  |