Different lymphscintigraphic patterns in patients with lymphedema distichiasis.
Identifieur interne : 005953 ( Main/Exploration ); précédent : 005952; suivant : 005954Different lymphscintigraphic patterns in patients with lymphedema distichiasis.
Auteurs : E. Sutkowska [Pologne] ; A. Bator ; K. Trompeta ; A. SzubaSource :
- Lymphology [ 0024-7766 ] ; 2010.
Descripteurs français
- KwdFr :
- MESH :
- imagerie diagnostique : Lymphoedème.
- malformations : Cils.
- Adulte, Adulte d'âge moyen, Enfant d'âge préscolaire, Femelle, Humains, Lymphoedème, Lymphoscintigraphie, Malformations lymphatiques, Mâle, Pedigree, Radiopharmaceutiques, Syndrome.
English descriptors
- KwdEn :
- MESH :
- chemical : Radiopharmaceuticals.
- abnormalities : Eyelashes.
- diagnostic imaging : Lymphedema.
- therapy : Lymphedema.
- Adult, Child, Preschool, Female, Humans, Lymphatic Abnormalities, Lymphoscintigraphy, Male, Middle Aged, Pedigree, Syndrome.
Abstract
Mutation of the transcription factor FOXC2 gene has been identified as the cause of lymphedema-distichiasis syndrome (LD). Subjects with LD usually present with lower extremity lymphedema and distichiasis--an additional row of eyelashes. Typically, lymphscintigrams of patients with LD show good transport of the radiotracer from the feet to the inguinal lymph nodes accompanied by reflux of tracer to the skin of the lower extremities ("dermal backflow"). We have examined two patients with LD syndrome and were able to demonstrate two different distinct lymphscintigraphic patterns: lymphatic hyperplasia with reflux and obstructive.
PubMed: 20848994
Affiliations:
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Sutkowska</name><affiliation wicri:level="1"><nlm:affiliation>Department and Clinic of Orthopaedic and Traumatologic Surgery, Wroclaw Medical University, Wroclaw, Poland.</nlm:affiliation><country xml:lang="fr">Pologne</country><wicri:regionArea>Department and Clinic of Orthopaedic and Traumatologic Surgery, Wroclaw Medical University, Wroclaw</wicri:regionArea><wicri:noRegion>Wroclaw</wicri:noRegion></affiliation></author><author><name sortKey="Bator, A" sort="Bator, A" uniqKey="Bator A" first="A" last="Bator">A. Bator</name></author><author><name sortKey="Trompeta, K" sort="Trompeta, K" uniqKey="Trompeta K" first="K" last="Trompeta">K. Trompeta</name></author><author><name sortKey="Szuba, A" sort="Szuba, A" uniqKey="Szuba A" first="A" last="Szuba">A. Szuba</name></author></analytic><series><title level="j">Lymphology</title><idno type="ISSN">0024-7766</idno><imprint><date when="2010" type="published">2010</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Child, Preschool</term><term>Eyelashes (abnormalities)</term><term>Female</term><term>Humans</term><term>Lymphatic Abnormalities</term><term>Lymphedema (diagnostic imaging)</term><term>Lymphedema (therapy)</term><term>Lymphoscintigraphy</term><term>Male</term><term>Middle Aged</term><term>Pedigree</term><term>Radiopharmaceuticals</term><term>Syndrome</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term><term>Adulte d'âge moyen</term><term>Cils (malformations)</term><term>Enfant d'âge préscolaire</term><term>Femelle</term><term>Humains</term><term>Lymphoedème ()</term><term>Lymphoedème (imagerie diagnostique)</term><term>Lymphoscintigraphie</term><term>Malformations lymphatiques</term><term>Mâle</term><term>Pedigree</term><term>Radiopharmaceutiques</term><term>Syndrome</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>Radiopharmaceuticals</term></keywords><keywords scheme="MESH" qualifier="abnormalities" xml:lang="en"><term>Eyelashes</term></keywords><keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="imagerie diagnostique" xml:lang="fr"><term>Lymphoedème</term></keywords><keywords scheme="MESH" qualifier="malformations" xml:lang="fr"><term>Cils</term></keywords><keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Child, Preschool</term><term>Female</term><term>Humans</term><term>Lymphatic Abnormalities</term><term>Lymphoscintigraphy</term><term>Male</term><term>Middle Aged</term><term>Pedigree</term><term>Syndrome</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adulte</term><term>Adulte d'âge moyen</term><term>Enfant d'âge préscolaire</term><term>Femelle</term><term>Humains</term><term>Lymphoedème</term><term>Lymphoscintigraphie</term><term>Malformations lymphatiques</term><term>Mâle</term><term>Pedigree</term><term>Radiopharmaceutiques</term><term>Syndrome</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Mutation of the transcription factor FOXC2 gene has been identified as the cause of lymphedema-distichiasis syndrome (LD). Subjects with LD usually present with lower extremity lymphedema and distichiasis--an additional row of eyelashes. Typically, lymphscintigrams of patients with LD show good transport of the radiotracer from the feet to the inguinal lymph nodes accompanied by reflux of tracer to the skin of the lower extremities ("dermal backflow"). We have examined two patients with LD syndrome and were able to demonstrate two different distinct lymphscintigraphic patterns: lymphatic hyperplasia with reflux and obstructive.</div></front></TEI><affiliations><list><country><li>Pologne</li></country></list><tree><noCountry><name sortKey="Bator, A" sort="Bator, A" uniqKey="Bator A" first="A" last="Bator">A. Bator</name><name sortKey="Szuba, A" sort="Szuba, A" uniqKey="Szuba A" first="A" last="Szuba">A. Szuba</name><name sortKey="Trompeta, K" sort="Trompeta, K" uniqKey="Trompeta K" first="K" last="Trompeta">K. Trompeta</name></noCountry><country name="Pologne"><noRegion><name sortKey="Sutkowska, E" sort="Sutkowska, E" uniqKey="Sutkowska E" first="E" last="Sutkowska">E. Sutkowska</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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