Diffuse lipofibromatosis of the lower extremity masquerading as a vascular anomaly.
Identifieur interne : 006324 ( Main/Exploration ); précédent : 006323; suivant : 006325Diffuse lipofibromatosis of the lower extremity masquerading as a vascular anomaly.
Auteurs : Arin K. Greene [États-Unis] ; Julie Karnes ; Horacio M. Padua ; Birgitta A. Schmidt ; James R. Kasser ; Brian I. LabowSource :
- Annals of plastic surgery [ 1536-3708 ] ; 2009.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
Abstract
Lipofibromatosis is a slow-growing, childhood soft-tissue neoplasm that is often confused with other conditions. We report a patient with lipofibromatosis causing extremity enlargement at birth. The lesion initially was thought to be a vascular anomaly or lipedema on clinical and MRI examination. When involving the lower extremity, diffuse lipofibromatosis must be differentiated from more common causes of lower limb enlargement in children: lymphatic malformation, lymphedema, or lipedema. Compared with these more frequent conditions, lipofibromatosis usually causes less morbidity. Management of the tumor includes observation or excision. Because complete extirpation of the lesion is difficult, the recurrence rate is high.
DOI: 10.1097/SAP.0b013e3181a13df6
PubMed: 19461290
Affiliations:
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Le document en format XML
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<author><name sortKey="Padua, Horacio M" sort="Padua, Horacio M" uniqKey="Padua H" first="Horacio M" last="Padua">Horacio M. Padua</name>
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<term>Humans</term>
<term>Infant</term>
<term>Lipomatosis (diagnosis)</term>
<term>Lower Extremity</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Soft Tissue Neoplasms (diagnosis)</term>
<term>Vascular Malformations (diagnosis)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Anomalies vasculaires (diagnostic)</term>
<term>Diagnostic différentiel</term>
<term>Fibrome (diagnostic)</term>
<term>Humains</term>
<term>Imagerie par résonance magnétique</term>
<term>Lipomatose (diagnostic)</term>
<term>Membre inférieur</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Tumeurs des tissus mous (diagnostic)</term>
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<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Anomalies vasculaires</term>
<term>Fibrome</term>
<term>Lipomatose</term>
<term>Tumeurs des tissus mous</term>
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<term>Humans</term>
<term>Infant</term>
<term>Lower Extremity</term>
<term>Magnetic Resonance Imaging</term>
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<term>Mâle</term>
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<front><div type="abstract" xml:lang="en">Lipofibromatosis is a slow-growing, childhood soft-tissue neoplasm that is often confused with other conditions. We report a patient with lipofibromatosis causing extremity enlargement at birth. The lesion initially was thought to be a vascular anomaly or lipedema on clinical and MRI examination. When involving the lower extremity, diffuse lipofibromatosis must be differentiated from more common causes of lower limb enlargement in children: lymphatic malformation, lymphedema, or lipedema. Compared with these more frequent conditions, lipofibromatosis usually causes less morbidity. Management of the tumor includes observation or excision. Because complete extirpation of the lesion is difficult, the recurrence rate is high.</div>
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<name sortKey="Kasser, James R" sort="Kasser, James R" uniqKey="Kasser J" first="James R" last="Kasser">James R. Kasser</name>
<name sortKey="Labow, Brian I" sort="Labow, Brian I" uniqKey="Labow B" first="Brian I" last="Labow">Brian I. Labow</name>
<name sortKey="Padua, Horacio M" sort="Padua, Horacio M" uniqKey="Padua H" first="Horacio M" last="Padua">Horacio M. Padua</name>
<name sortKey="Schmidt, Birgitta A" sort="Schmidt, Birgitta A" uniqKey="Schmidt B" first="Birgitta A" last="Schmidt">Birgitta A. Schmidt</name>
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<country name="États-Unis"><region name="Massachusetts"><name sortKey="Greene, Arin K" sort="Greene, Arin K" uniqKey="Greene A" first="Arin K" last="Greene">Arin K. Greene</name>
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