Congenital elephantiasis-like lymphangiomatosis of a lower limb.
Identifieur interne : 000617 ( France/Analysis ); précédent : 000616; suivant : 000618Congenital elephantiasis-like lymphangiomatosis of a lower limb.
Auteurs : Astrid Imiela [France] ; Delphine Salle-Staumont ; Georges-Marie Breviere ; Benoit Catteau ; Veronique Martinot-Duquennoy ; Frederic PietteSource :
- Acta dermato-venereologica [ 0001-5555 ] ; 2003.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Lymphangiome, Tumeurs cutanées.
- diagnostic : Lymphangiome, Tumeurs cutanées, Éléphantiasis.
- Diagnostic différentiel, Femelle, Humains, Jambe, Lymphangiome, Nouveau-né, Tumeurs cutanées.
English descriptors
- KwdEn :
- Diagnosis, Differential, Elephantiasis (diagnosis), Female, Humans, Infant, Newborn, Leg, Lymphangioma (congenital), Lymphangioma (diagnosis), Lymphangioma (pathology), Lymphangioma (therapy), Skin Neoplasms (congenital), Skin Neoplasms (diagnosis), Skin Neoplasms (pathology), Skin Neoplasms (therapy).
- MESH :
- congenital : Lymphangioma, Skin Neoplasms.
- diagnosis : Elephantiasis, Lymphangioma, Skin Neoplasms.
- pathology : Lymphangioma, Skin Neoplasms.
- therapy : Lymphangioma, Skin Neoplasms.
- Diagnosis, Differential, Female, Humans, Infant, Newborn, Leg.
Abstract
The case of a newborn girl with a rare, giant, congenital, tissue lymphangioma giving rise to elephantiasis of the right lower limb is presented. The different imaging methods, especially magnetic resonance imaging, showed no extension of the lesions into the deep structures. At the age of 2 years, the child underwent a roentgenographic skeletal survey, which revealed osteolytic lesions in the femurs and the right tibia. There was no clinical evidence of systemic involvement. The place of this affection among the different lymphatic malformations was discussed and the diagnosis of elephantiasis-like lymphangiomatosis of the limb, an extremely rare disorder, has been retained. Early surgical reduction was performed, followed by application of a pressure dressing. Five years later the result remains satisfactory, but the excision of a persistent fluid-filled pouch around the knee will probably be necessary in the future.
PubMed: 12636021
Affiliations:
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pubmed:12636021Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Congenital elephantiasis-like lymphangiomatosis of a lower limb.</title>
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<author><name sortKey="Salle Staumont, Delphine" sort="Salle Staumont, Delphine" uniqKey="Salle Staumont D" first="Delphine" last="Salle-Staumont">Delphine Salle-Staumont</name>
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<author><name sortKey="Breviere, Georges Marie" sort="Breviere, Georges Marie" uniqKey="Breviere G" first="Georges-Marie" last="Breviere">Georges-Marie Breviere</name>
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<author><name sortKey="Martinot Duquennoy, Veronique" sort="Martinot Duquennoy, Veronique" uniqKey="Martinot Duquennoy V" first="Veronique" last="Martinot-Duquennoy">Veronique Martinot-Duquennoy</name>
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<term>Elephantiasis (diagnosis)</term>
<term>Female</term>
<term>Humans</term>
<term>Infant, Newborn</term>
<term>Leg</term>
<term>Lymphangioma (congenital)</term>
<term>Lymphangioma (diagnosis)</term>
<term>Lymphangioma (pathology)</term>
<term>Lymphangioma (therapy)</term>
<term>Skin Neoplasms (congenital)</term>
<term>Skin Neoplasms (diagnosis)</term>
<term>Skin Neoplasms (pathology)</term>
<term>Skin Neoplasms (therapy)</term>
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<term>Femelle</term>
<term>Humains</term>
<term>Jambe</term>
<term>Lymphangiome ()</term>
<term>Lymphangiome (anatomopathologie)</term>
<term>Lymphangiome (diagnostic)</term>
<term>Nouveau-né</term>
<term>Tumeurs cutanées ()</term>
<term>Tumeurs cutanées (anatomopathologie)</term>
<term>Tumeurs cutanées (diagnostic)</term>
<term>Éléphantiasis (diagnostic)</term>
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<term>Tumeurs cutanées</term>
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<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Elephantiasis</term>
<term>Lymphangioma</term>
<term>Skin Neoplasms</term>
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<term>Tumeurs cutanées</term>
<term>Éléphantiasis</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Lymphangioma</term>
<term>Skin Neoplasms</term>
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<term>Humans</term>
<term>Infant, Newborn</term>
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<front><div type="abstract" xml:lang="en">The case of a newborn girl with a rare, giant, congenital, tissue lymphangioma giving rise to elephantiasis of the right lower limb is presented. The different imaging methods, especially magnetic resonance imaging, showed no extension of the lesions into the deep structures. At the age of 2 years, the child underwent a roentgenographic skeletal survey, which revealed osteolytic lesions in the femurs and the right tibia. There was no clinical evidence of systemic involvement. The place of this affection among the different lymphatic malformations was discussed and the diagnosis of elephantiasis-like lymphangiomatosis of the limb, an extremely rare disorder, has been retained. Early surgical reduction was performed, followed by application of a pressure dressing. Five years later the result remains satisfactory, but the excision of a persistent fluid-filled pouch around the knee will probably be necessary in the future.</div>
</front>
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<name sortKey="Catteau, Benoit" sort="Catteau, Benoit" uniqKey="Catteau B" first="Benoit" last="Catteau">Benoit Catteau</name>
<name sortKey="Martinot Duquennoy, Veronique" sort="Martinot Duquennoy, Veronique" uniqKey="Martinot Duquennoy V" first="Veronique" last="Martinot-Duquennoy">Veronique Martinot-Duquennoy</name>
<name sortKey="Piette, Frederic" sort="Piette, Frederic" uniqKey="Piette F" first="Frederic" last="Piette">Frederic Piette</name>
<name sortKey="Salle Staumont, Delphine" sort="Salle Staumont, Delphine" uniqKey="Salle Staumont D" first="Delphine" last="Salle-Staumont">Delphine Salle-Staumont</name>
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<country name="France"><noRegion><name sortKey="Imiela, Astrid" sort="Imiela, Astrid" uniqKey="Imiela A" first="Astrid" last="Imiela">Astrid Imiela</name>
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