LymphedemaV1, PascalFrancis, Corpus, bibRecord, 000631

Stewart-Treves syndrome as a rare complication of a hereditary lymphedema

Identifieur interne : 000631 ( PascalFrancis/Corpus ); précédent : 000630; suivant : 000632

Stewart-Treves syndrome as a rare complication of a hereditary lymphedema

Auteurs : H. R. Dürr ; C. Pellengahr ; A. Nerlich ; A. Baur ; M. Maier ; V. Jansson

Source :

VASA [ 0301-1526 ] ; 2004.

RBID : Pascal:04-0365449

Descripteurs français

Pascal (Inist)
- Lymphoedème, Complication, Appareil circulatoire pathologie.

English descriptors

KwdEn :
- Cardiovascular disease, Complication, Lymphedema.

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.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

A01	`01`	`1`		`@0 0301-1526`
A02	`01`			`@0 VASAAH`
A03		`1`		`@0 VASA`
A05				`@2 33`
A06				`@2 1`
A08	`01`	`1`	`ENG`	`@1 Stewart-Treves syndrome as a rare complication of a hereditary lymphedema`
A11	`01`	`1`		`@1 DÜRR (H. R.)`
A11	`02`	`1`		`@1 PELLENGAHR (C.)`
A11	`03`	`1`		`@1 NERLICH (A.)`
A11	`04`	`1`		`@1 BAUR (A.)`
A11	`05`	`1`		`@1 MAIER (M.)`
A11	`06`	`1`		`@1 JANSSON (V.)`
A14	`01`			`@1 Department of Orthopaedics and Orthopaedic Surgery, Ludwig-Maximilians-University Munich @3 DEU @Z 1 aut. @Z 2 aut. @Z 5 aut. @Z 6 aut.`
A14	`02`			`@1 Institute of Pathology, Krankenhaus München Bogenhausen @3 DEU @Z 3 aut.`
A14	`03`			`@1 Institute of Radiology, Ludwig-Maximilians-University Munich @3 DEU @Z 4 aut.`
A20				`@1 42-45`
A21				`@1 2004`
A23	`01`			`@0 ENG`
A24	`01`			`@0 ger`
A43	`01`			`@1 INIST @2 10984 @5 354000119282810070`
A44				`@0 0000 @1 © 2004 INIST-CNRS. All rights reserved.`
A45				`@0 36 ref.`
A47	`01`	`1`		`@0 04-0365449`
A60				`@1 P @3 EC`
A61				`@0 A`
A64	`01`	`1`		`@0 VASA`
A66	`01`			`@0 CHE`
C01	`01`		`ENG`	`@0 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.`
C02	`01`	`X`		`@0 002B12B03`
C03	`01`	`X`	`FRE`	`@0 Lymphoedème @5 01`
C03	`01`	`X`	`ENG`	`@0 Lymphedema @5 01`
C03	`01`	`X`	`SPA`	`@0 Linfedema @5 01`
C03	`02`	`X`	`FRE`	`@0 Complication @5 02`
C03	`02`	`X`	`ENG`	`@0 Complication @5 02`
C03	`02`	`X`	`SPA`	`@0 Complicación @5 02`
C03	`03`	`X`	`FRE`	`@0 Appareil circulatoire pathologie @5 04`
C03	`03`	`X`	`ENG`	`@0 Cardiovascular disease @5 04`
C03	`03`	`X`	`SPA`	`@0 Aparato circulatorio patología @5 04`
C07	`01`	`X`	`FRE`	`@0 Lymphatique pathologie @5 37`
C07	`01`	`X`	`ENG`	`@0 Lymphatic vessel disease @5 37`
C07	`01`	`X`	`SPA`	`@0 Linfático patología @5 37`
N21				`@1 208`
N44	`01`			`@1 OTO`
N82				`@1 OTO`

Format Inist (serveur)

NO :	PASCAL 04-0365449 INIST
ET :	Stewart-Treves syndrome as a rare complication of a hereditary lymphedema
AU :	DÜRR (H. R.); PELLENGAHR (C.); NERLICH (A.); BAUR (A.); MAIER (M.); JANSSON (V.)
AF :	Department of Orthopaedics and Orthopaedic Surgery, Ludwig-Maximilians-University Munich/Allemagne (1 aut., 2 aut., 5 aut., 6 aut.); Institute of Pathology, Krankenhaus München Bogenhausen/Allemagne (3 aut.); Institute of Radiology, Ludwig-Maximilians-University Munich/Allemagne (4 aut.)
DT :	Publication en série; Etude de cas, cas et faits cliniques; Niveau analytique
SO :	VASA; ISSN 0301-1526; Coden VASAAH; Suisse; Da. 2004; Vol. 33; No. 1; Pp. 42-45; Abs. allemand; Bibl. 36 ref.
LA :	Anglais
EA :	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.
CC :	002B12B03
FD :	Lymphoedème; Complication; Appareil circulatoire pathologie
FG :	Lymphatique pathologie
ED :	Lymphedema; Complication; Cardiovascular disease
EG :	Lymphatic vessel disease
SD :	Linfedema; Complicación; Aparato circulatorio patología
LO :	INIST-10984.354000119282810070
ID :	04-0365449

Links to Exploration step

Pascal:04-0365449

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Stewart-Treves syndrome as a rare complication of a hereditary lymphedema</title>
<author><name sortKey="Durr, H R" sort="Durr, H R" uniqKey="Durr H" first="H. R." last="Dürr">H. R. Dürr</name>
<affiliation><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>
</affiliation>
</author>
<author><name sortKey="Pellengahr, C" sort="Pellengahr, C" uniqKey="Pellengahr C" first="C." last="Pellengahr">C. Pellengahr</name>
<affiliation><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>
</affiliation>
</author>
<author><name sortKey="Nerlich, A" sort="Nerlich, A" uniqKey="Nerlich A" first="A." last="Nerlich">A. Nerlich</name>
<affiliation><inist:fA14 i1="02"><s1>Institute of Pathology, Krankenhaus München Bogenhausen</s1>
<s3>DEU</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Baur, A" sort="Baur, A" uniqKey="Baur A" first="A." last="Baur">A. Baur</name>
<affiliation><inist:fA14 i1="03"><s1>Institute of Radiology, Ludwig-Maximilians-University Munich</s1>
<s3>DEU</s3>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Maier, M" sort="Maier, M" uniqKey="Maier M" first="M." last="Maier">M. Maier</name>
<affiliation><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>
</affiliation>
</author>
<author><name sortKey="Jansson, V" sort="Jansson, V" uniqKey="Jansson V" first="V." last="Jansson">V. Jansson</name>
<affiliation><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>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">04-0365449</idno>
<date when="2004">2004</date>
<idno type="stanalyst">PASCAL 04-0365449 INIST</idno>
<idno type="RBID">Pascal:04-0365449</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000631</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Stewart-Treves syndrome as a rare complication of a hereditary lymphedema</title>
<author><name sortKey="Durr, H R" sort="Durr, H R" uniqKey="Durr H" first="H. R." last="Dürr">H. R. Dürr</name>
<affiliation><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>
</affiliation>
</author>
<author><name sortKey="Pellengahr, C" sort="Pellengahr, C" uniqKey="Pellengahr C" first="C." last="Pellengahr">C. Pellengahr</name>
<affiliation><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>
</affiliation>
</author>
<author><name sortKey="Nerlich, A" sort="Nerlich, A" uniqKey="Nerlich A" first="A." last="Nerlich">A. Nerlich</name>
<affiliation><inist:fA14 i1="02"><s1>Institute of Pathology, Krankenhaus München Bogenhausen</s1>
<s3>DEU</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Baur, A" sort="Baur, A" uniqKey="Baur A" first="A." last="Baur">A. Baur</name>
<affiliation><inist:fA14 i1="03"><s1>Institute of Radiology, Ludwig-Maximilians-University Munich</s1>
<s3>DEU</s3>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Maier, M" sort="Maier, M" uniqKey="Maier M" first="M." last="Maier">M. Maier</name>
<affiliation><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>
</affiliation>
</author>
<author><name sortKey="Jansson, V" sort="Jansson, V" uniqKey="Jansson V" first="V." last="Jansson">V. Jansson</name>
<affiliation><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>
</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>Cardiovascular disease</term>
<term>Complication</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Lymphoedème</term>
<term>Complication</term>
<term>Appareil circulatoire pathologie</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>
<inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0301-1526</s0>
</fA01>
<fA02 i1="01"><s0>VASAAH</s0>
</fA02>
<fA03 i2="1"><s0>VASA</s0>
</fA03>
<fA05><s2>33</s2>
</fA05>
<fA06><s2>1</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG"><s1>Stewart-Treves syndrome as a rare complication of a hereditary lymphedema</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>DÜRR (H. R.)</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>PELLENGAHR (C.)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>NERLICH (A.)</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>BAUR (A.)</s1>
</fA11>
<fA11 i1="05" i2="1"><s1>MAIER (M.)</s1>
</fA11>
<fA11 i1="06" i2="1"><s1>JANSSON (V.)</s1>
</fA11>
<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>
</fA14>
<fA14 i1="02"><s1>Institute of Pathology, Krankenhaus München Bogenhausen</s1>
<s3>DEU</s3>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="03"><s1>Institute of Radiology, Ludwig-Maximilians-University Munich</s1>
<s3>DEU</s3>
<sZ>4 aut.</sZ>
</fA14>
<fA20><s1>42-45</s1>
</fA20>
<fA21><s1>2004</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
<fA24 i1="01"><s0>ger</s0>
</fA24>
<fA43 i1="01"><s1>INIST</s1>
<s2>10984</s2>
<s5>354000119282810070</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2004 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>36 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>04-0365449</s0>
</fA47>
<fA60><s1>P</s1>
<s3>EC</s3>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>VASA</s0>
</fA64>
<fA66 i1="01"><s0>CHE</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>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.</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>002B12B03</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE"><s0>Lymphoedème</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG"><s0>Lymphedema</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Linfedema</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE"><s0>Complication</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Complication</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Complicación</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Appareil circulatoire pathologie</s0>
<s5>04</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Cardiovascular disease</s0>
<s5>04</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Aparato circulatorio patología</s0>
<s5>04</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Lymphatique pathologie</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Lymphatic vessel disease</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Linfático patología</s0>
<s5>37</s5>
</fC07>
<fN21><s1>208</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
<server><NO>PASCAL 04-0365449 INIST</NO>
<ET>Stewart-Treves syndrome as a rare complication of a hereditary lymphedema</ET>
<AU>DÜRR (H. R.); PELLENGAHR (C.); NERLICH (A.); BAUR (A.); MAIER (M.); JANSSON (V.)</AU>
<AF>Department of Orthopaedics and Orthopaedic Surgery, Ludwig-Maximilians-University Munich/Allemagne (1 aut., 2 aut., 5 aut., 6 aut.); Institute of Pathology, Krankenhaus München Bogenhausen/Allemagne (3 aut.); Institute of Radiology, Ludwig-Maximilians-University Munich/Allemagne (4 aut.)</AF>
<DT>Publication en série; Etude de cas, cas et faits cliniques; Niveau analytique</DT>
<SO>VASA; ISSN 0301-1526; Coden VASAAH; Suisse; Da. 2004; Vol. 33; No. 1; Pp. 42-45; Abs. allemand; Bibl. 36 ref.</SO>
<LA>Anglais</LA>
<EA>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.</EA>
<CC>002B12B03</CC>
<FD>Lymphoedème; Complication; Appareil circulatoire pathologie</FD>
<FG>Lymphatique pathologie</FG>
<ED>Lymphedema; Complication; Cardiovascular disease</ED>
<EG>Lymphatic vessel disease</EG>
<SD>Linfedema; Complicación; Aparato circulatorio patología</SD>
<LO>INIST-10984.354000119282810070</LO>
<ID>04-0365449</ID>
</server>
</inist>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/PascalFrancis/Corpus

HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000631 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/PascalFrancis/Corpus/biblio.hfd -nk 000631 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Sante
   |area=    LymphedemaV1
   |flux=    PascalFrancis
   |étape=   Corpus
   |type=    RBID
   |clé=     Pascal:04-0365449
   |texte=   Stewart-Treves syndrome as a rare complication of a hereditary lymphedema
}}

This area was generated with Dilib version V0.6.31.
Data generation: Sat Nov 4 17:40:35 2017. Site generation: Tue Feb 13 16:42:16 2024

	Serveur d'exploration sur le lymphœdème
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.

Serveur d'exploration sur le lymphœdème

Stewart-Treves syndrome as a rare complication of a hereditary lymphedema

Stewart-Treves syndrome as a rare complication of a hereditary lymphedema

Source :

Descripteurs français

English descriptors

Abstract

Notice en format standard (ISO 2709)

Format Inist (serveur)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri