Stewart-Treves syndrome as a rare complication of a hereditary lymphedema
Identifieur interne : 008D00 ( Main/Exploration ); précédent : 008C99; suivant : 008D01Stewart-Treves syndrome as a rare complication of a hereditary lymphedema
Auteurs : H. R. Dürr [Allemagne] ; C. Pellengahr [Allemagne] ; A. Nerlich [Allemagne] ; A. Baur [Allemagne] ; M. Maier [Allemagne] ; V. Jansson [Allemagne]Source :
- VASA [ 0301-1526 ] ; 2004.
Descripteurs français
- KwdFr :
- Adulte, Amputation chirurgicale, Antigènes CD31 (analyse), Biopsie, Femelle, Gènes dominants, Humains, Imagerie par résonance magnétique, Invasion tumorale (anatomopathologie), Issue fatale, Jambe (anatomopathologie), Lymphangiosarcome (), Lymphangiosarcome (anatomopathologie), Lymphangiosarcome (diagnostic), Lymphoedème (), Lymphoedème (anatomopathologie), Lymphoedème (diagnostic), Lymphoedème (génétique), Peau (anatomopathologie), Prédisposition génétique à une maladie (génétique), Syndrome, Tumeurs cutanées (), Tumeurs cutanées (anatomopathologie), Tumeurs cutanées (diagnostic), Tumeurs des tissus mous (), Tumeurs des tissus mous (anatomopathologie), Tumeurs des tissus mous (diagnostic), Évolution de la maladie.
- MESH :
- analyse : Antigènes CD31.
- anatomopathologie : Invasion tumorale, Jambe, Lymphangiosarcome, Lymphoedème, Peau, Tumeurs cutanées, Tumeurs des tissus mous.
- diagnostic : Lymphangiosarcome, Lymphoedème, Tumeurs cutanées, Tumeurs des tissus mous.
- génétique : Lymphoedème, Prédisposition génétique à une maladie.
- Pascal (Inist)
English descriptors
- KwdEn :
- Adult, Amputation, Antigens, CD31 (analysis), Biopsy, Cardiovascular disease, Complication, Disease Progression, Fatal Outcome, Female, Genes, Dominant, Genetic Predisposition to Disease (genetics), Humans, Leg (pathology), Lymphangiosarcoma (diagnosis), Lymphangiosarcoma (pathology), Lymphangiosarcoma (surgery), Lymphedema, Lymphedema (complications), Lymphedema (diagnosis), Lymphedema (genetics), Lymphedema (pathology), Magnetic Resonance Imaging, Neoplasm Invasiveness (pathology), Skin (pathology), Skin Neoplasms (diagnosis), Skin Neoplasms (pathology), Skin Neoplasms (surgery), Soft Tissue Neoplasms (diagnosis), Soft Tissue Neoplasms (pathology), Soft Tissue Neoplasms (surgery), Syndrome.
- MESH :
- chemical , analysis : Antigens, CD31.
- complications : Lymphedema.
- diagnosis : Lymphangiosarcoma, Lymphedema, Skin Neoplasms, Soft Tissue Neoplasms.
- genetics : Genetic Predisposition to Disease, Lymphedema.
- pathology : Leg, Lymphangiosarcoma, Lymphedema, Neoplasm Invasiveness, Skin, Skin Neoplasms, Soft Tissue Neoplasms.
- surgery : Lymphangiosarcoma, Skin Neoplasms, Soft Tissue Neoplasms.
- Adult, Amputation, Biopsy, Disease Progression, Fatal Outcome, Female, Genes, Dominant, Humans, Magnetic Resonance Imaging, Syndrome.
Abstract
Lymphangiosarcoma (LAS) may occur as a rare complication of primary lymphedema. A case of LAS in hereditary lymphedema of the lower extremity in a 36-year old female is reported. Despite of chemotherapy, local hyperthermia and later amputation of the extremity the patient died of progressive disease due to pulmonary metastasis. In respect to this case, the different therapeutic concepts, as reported in the literature, and their results are presented and discussed.
Affiliations:
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R." last="Dürr">H. R. Dürr</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Orthopaedics and Orthopaedic Surgery, Ludwig-Maximilians-University Munich</s1><s3>DEU</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14><country>Allemagne</country><wicri:noRegion>Ludwig-Maximilians-University Munich</wicri:noRegion><wicri:noRegion>Department of Orthopaedics and Orthopaedic Surgery, Ludwig-Maximilians-University Munich</wicri:noRegion></affiliation></author><author><name sortKey="Pellengahr, C" sort="Pellengahr, C" uniqKey="Pellengahr C" first="C." last="Pellengahr">C. Pellengahr</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Orthopaedics and Orthopaedic Surgery, Ludwig-Maximilians-University Munich</s1><s3>DEU</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14><country>Allemagne</country><wicri:noRegion>Ludwig-Maximilians-University Munich</wicri:noRegion><wicri:noRegion>Department of Orthopaedics and Orthopaedic Surgery, Ludwig-Maximilians-University Munich</wicri:noRegion></affiliation></author><author><name sortKey="Nerlich, A" sort="Nerlich, A" uniqKey="Nerlich A" first="A." last="Nerlich">A. Nerlich</name><affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Institute of Pathology, Krankenhaus München Bogenhausen</s1><s3>DEU</s3><sZ>3 aut.</sZ></inist:fA14><country>Allemagne</country><wicri:noRegion>Krankenhaus München Bogenhausen</wicri:noRegion><wicri:noRegion>Institute of Pathology, Krankenhaus München Bogenhausen</wicri:noRegion></affiliation></author><author><name sortKey="Baur, A" sort="Baur, A" uniqKey="Baur A" first="A." last="Baur">A. Baur</name><affiliation wicri:level="1"><inist:fA14 i1="03"><s1>Institute of Radiology, Ludwig-Maximilians-University Munich</s1><s3>DEU</s3><sZ>4 aut.</sZ></inist:fA14><country>Allemagne</country><wicri:noRegion>Ludwig-Maximilians-University Munich</wicri:noRegion><wicri:noRegion>Institute of Radiology, Ludwig-Maximilians-University Munich</wicri:noRegion></affiliation></author><author><name sortKey="Maier, M" sort="Maier, M" uniqKey="Maier M" first="M." last="Maier">M. Maier</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Orthopaedics and Orthopaedic Surgery, Ludwig-Maximilians-University Munich</s1><s3>DEU</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14><country>Allemagne</country><wicri:noRegion>Ludwig-Maximilians-University Munich</wicri:noRegion><wicri:noRegion>Department of Orthopaedics and Orthopaedic Surgery, Ludwig-Maximilians-University Munich</wicri:noRegion></affiliation></author><author><name sortKey="Jansson, V" sort="Jansson, V" uniqKey="Jansson V" first="V." last="Jansson">V. Jansson</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Orthopaedics and Orthopaedic Surgery, Ludwig-Maximilians-University Munich</s1><s3>DEU</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14><country>Allemagne</country><wicri:noRegion>Ludwig-Maximilians-University Munich</wicri:noRegion><wicri:noRegion>Department of Orthopaedics and Orthopaedic Surgery, Ludwig-Maximilians-University Munich</wicri:noRegion></affiliation></author></analytic><series><title level="j" type="main">VASA</title><title level="j" type="abbreviated">VASA</title><idno type="ISSN">0301-1526</idno><imprint><date when="2004">2004</date></imprint></series></biblStruct></sourceDesc><seriesStmt><title level="j" type="main">VASA</title><title level="j" type="abbreviated">VASA</title><idno type="ISSN">0301-1526</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Amputation</term><term>Antigens, CD31 (analysis)</term><term>Biopsy</term><term>Cardiovascular disease</term><term>Complication</term><term>Disease Progression</term><term>Fatal Outcome</term><term>Female</term><term>Genes, Dominant</term><term>Genetic Predisposition to Disease (genetics)</term><term>Humans</term><term>Leg (pathology)</term><term>Lymphangiosarcoma (diagnosis)</term><term>Lymphangiosarcoma (pathology)</term><term>Lymphangiosarcoma (surgery)</term><term>Lymphedema</term><term>Lymphedema (complications)</term><term>Lymphedema (diagnosis)</term><term>Lymphedema (genetics)</term><term>Lymphedema (pathology)</term><term>Magnetic Resonance Imaging</term><term>Neoplasm Invasiveness (pathology)</term><term>Skin (pathology)</term><term>Skin Neoplasms (diagnosis)</term><term>Skin Neoplasms (pathology)</term><term>Skin Neoplasms (surgery)</term><term>Soft Tissue Neoplasms (diagnosis)</term><term>Soft Tissue Neoplasms (pathology)</term><term>Soft Tissue Neoplasms (surgery)</term><term>Syndrome</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term><term>Amputation chirurgicale</term><term>Antigènes CD31 (analyse)</term><term>Biopsie</term><term>Femelle</term><term>Gènes dominants</term><term>Humains</term><term>Imagerie par résonance magnétique</term><term>Invasion tumorale (anatomopathologie)</term><term>Issue fatale</term><term>Jambe (anatomopathologie)</term><term>Lymphangiosarcome ()</term><term>Lymphangiosarcome (anatomopathologie)</term><term>Lymphangiosarcome (diagnostic)</term><term>Lymphoedème ()</term><term>Lymphoedème (anatomopathologie)</term><term>Lymphoedème (diagnostic)</term><term>Lymphoedème (génétique)</term><term>Peau (anatomopathologie)</term><term>Prédisposition génétique à une maladie (génétique)</term><term>Syndrome</term><term>Tumeurs cutanées ()</term><term>Tumeurs cutanées (anatomopathologie)</term><term>Tumeurs cutanées (diagnostic)</term><term>Tumeurs des tissus mous ()</term><term>Tumeurs des tissus mous (anatomopathologie)</term><term>Tumeurs des tissus mous (diagnostic)</term><term>Évolution de la maladie</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Antigens, CD31</term></keywords><keywords scheme="MESH" qualifier="analyse" xml:lang="fr"><term>Antigènes CD31</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Invasion tumorale</term><term>Jambe</term><term>Lymphangiosarcome</term><term>Lymphoedème</term><term>Peau</term><term>Tumeurs cutanées</term><term>Tumeurs des tissus mous</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Lymphangiosarcoma</term><term>Lymphedema</term><term>Skin Neoplasms</term><term>Soft Tissue Neoplasms</term></keywords><keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Lymphangiosarcome</term><term>Lymphoedème</term><term>Tumeurs cutanées</term><term>Tumeurs des tissus mous</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Genetic Predisposition to Disease</term><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Lymphoedème</term><term>Prédisposition génétique à une maladie</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Leg</term><term>Lymphangiosarcoma</term><term>Lymphedema</term><term>Neoplasm Invasiveness</term><term>Skin</term><term>Skin Neoplasms</term><term>Soft Tissue Neoplasms</term></keywords><keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Lymphangiosarcoma</term><term>Skin Neoplasms</term><term>Soft Tissue Neoplasms</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Amputation</term><term>Biopsy</term><term>Disease Progression</term><term>Fatal Outcome</term><term>Female</term><term>Genes, Dominant</term><term>Humans</term><term>Magnetic Resonance Imaging</term><term>Syndrome</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Adulte</term><term>Amputation chirurgicale</term><term>Biopsie</term><term>Femelle</term><term>Gènes dominants</term><term>Humains</term><term>Imagerie par résonance magnétique</term><term>Issue fatale</term><term>Lymphangiosarcome</term><term>Lymphoedème</term><term>Complication</term><term>Appareil circulatoire pathologie</term><term>Syndrome</term><term>Tumeurs cutanées</term><term>Tumeurs des tissus mous</term><term>Évolution de la maladie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Lymphangiosarcoma (LAS) may occur as a rare complication of primary lymphedema. A case of LAS in hereditary lymphedema of the lower extremity in a 36-year old female is reported. Despite of chemotherapy, local hyperthermia and later amputation of the extremity the patient died of progressive disease due to pulmonary metastasis. In respect to this case, the different therapeutic concepts, as reported in the literature, and their results are presented and discussed.</div></front></TEI><affiliations><list><country><li>Allemagne</li></country></list><tree><country name="Allemagne"><noRegion><name sortKey="Durr, H R" sort="Durr, H R" uniqKey="Durr H" first="H. R." last="Dürr">H. R. Dürr</name></noRegion><name sortKey="Baur, A" sort="Baur, A" uniqKey="Baur A" first="A." last="Baur">A. Baur</name><name sortKey="Jansson, V" sort="Jansson, V" uniqKey="Jansson V" first="V." last="Jansson">V. Jansson</name><name sortKey="Maier, M" sort="Maier, M" uniqKey="Maier M" first="M." last="Maier">M. Maier</name><name sortKey="Nerlich, A" sort="Nerlich, A" uniqKey="Nerlich A" first="A." last="Nerlich">A. Nerlich</name><name sortKey="Pellengahr, C" sort="Pellengahr, C" uniqKey="Pellengahr C" first="C." last="Pellengahr">C. Pellengahr</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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