Lymphedema-induced lymphangiosarcoma
Identifieur interne : 00C570 ( Main/Exploration ); précédent : 00C569; suivant : 00C571Lymphedema-induced lymphangiosarcoma
Auteurs : Arieke J. Janse [Pays-Bas] ; Frits Van Coevorden [Pays-Bas] ; Hans Peterse [Pays-Bas] ; Ronald B. Keus [Pays-Bas] ; Johannes A. Van Dongen [Pays-Bas]Source :
- European Journal of Surgical Oncology [ 0748-7983 ] ; 1995.
Descripteurs français
- KwdFr :
- MESH :
- diagnostic : Lymphangiosarcome.
- effets indésirables : Association thérapeutique.
- étiologie : Lymphangiosarcome, Lymphoedème.
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Aged, Breast Neoplasms (complications), Breast Neoplasms (therapy), Combined Modality Therapy (adverse effects), Complication, Female, Human, Humans, Lymphangiosarcoma, Lymphangiosarcoma (diagnosis), Lymphangiosarcoma (etiology), Lymphangiosarcoma (therapy), Lymphedema, Lymphedema (complications), Lymphedema (congenital), Lymphedema (etiology), Male, Middle Aged, Stewart-Treves syndrome, angiosarcoma, breast carcinoma, lymphangiosarcoma, lymphedema.
- MESH :
- adverse effects : Combined Modality Therapy.
- complications : Breast Neoplasms, Lymphedema.
- congenital : Lymphedema.
- diagnosis : Lymphangiosarcoma.
- etiology : Lymphangiosarcoma, Lymphedema.
- therapy : Breast Neoplasms, Lymphangiosarcoma.
- Aged, Female, Humans, Male, Middle Aged.
Abstract
A series of eight patients with chronic lymphedema-related lymphangiosarcoma is presented. All but one case showed a typical rapid progression and fatal outcome, as has been reported in other series. In one patient the lymphangiosarcoma developed on the chest wall, the axilla and the arm where persisting lymphedema and fibrosis occurred after bilateral mastectomy and bilateral postoperative radiotherapy. In this patient an asymptomatic course and slow locoregional progression of lesions was seen. The clinical picture, the etiological considerations and the therapeutic options of the lymphedema-induced lymphangiosarcoma with regard to the literature are discussed.
Url:
DOI: 10.1016/S0748-7983(95)90270-8
Affiliations:
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Le document en format XML
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Janse</name><affiliation wicri:level="3"><country xml:lang="fr">Pays-Bas</country><wicri:regionArea>Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam</wicri:regionArea><placeName><settlement type="city">Amsterdam</settlement><region nuts="2" type="province">Hollande-Septentrionale</region></placeName></affiliation></author><author><name sortKey="Coevorden, Frits Van" sort="Coevorden, Frits Van" uniqKey="Coevorden F" first="Frits Van" last="Coevorden">Frits Van Coevorden</name><affiliation wicri:level="1"><country xml:lang="fr">Pays-Bas</country><wicri:regionArea>Correspondence to: F. van Coevorden, MD, PhD, Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Plesmanlaan 121, 1066 CX Amsterdam</wicri:regionArea><wicri:noRegion>1066 CX Amsterdam</wicri:noRegion></affiliation></author><author><name sortKey="Peterse, Hans" sort="Peterse, Hans" uniqKey="Peterse H" first="Hans" last="Peterse">Hans Peterse</name><affiliation wicri:level="3"><country xml:lang="fr">Pays-Bas</country><wicri:regionArea>Department of Pathology, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam</wicri:regionArea><placeName><settlement type="city">Amsterdam</settlement><region nuts="2" type="province">Hollande-Septentrionale</region></placeName></affiliation></author><author><name sortKey="Keus, Ronald B" sort="Keus, Ronald B" uniqKey="Keus R" first="Ronald B." last="Keus">Ronald B. Keus</name><affiliation wicri:level="3"><country xml:lang="fr">Pays-Bas</country><wicri:regionArea>Department of Radiotherapy, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam</wicri:regionArea><placeName><settlement type="city">Amsterdam</settlement><region nuts="2" type="province">Hollande-Septentrionale</region></placeName></affiliation></author><author><name sortKey="Dongen, Johannes A Van" sort="Dongen, Johannes A Van" uniqKey="Dongen J" first="Johannes A. Van" last="Dongen">Johannes A. Van Dongen</name><affiliation wicri:level="3"><country xml:lang="fr">Pays-Bas</country><wicri:regionArea>Department of Surgery, The Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam</wicri:regionArea><placeName><settlement type="city">Amsterdam</settlement><region nuts="2" type="province">Hollande-Septentrionale</region></placeName></affiliation></author></analytic><monogr></monogr><series><title level="j">European Journal of Surgical Oncology</title><title level="j" type="abbrev">YEJSO</title><idno type="ISSN">0748-7983</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1995">1995</date><biblScope unit="volume">21</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="155">155</biblScope><biblScope unit="page" to="158">158</biblScope></imprint><idno type="ISSN">0748-7983</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0748-7983</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Breast Neoplasms (complications)</term><term>Breast Neoplasms (therapy)</term><term>Combined Modality Therapy (adverse effects)</term><term>Complication</term><term>Female</term><term>Human</term><term>Humans</term><term>Lymphangiosarcoma</term><term>Lymphangiosarcoma (diagnosis)</term><term>Lymphangiosarcoma (etiology)</term><term>Lymphangiosarcoma (therapy)</term><term>Lymphedema</term><term>Lymphedema (complications)</term><term>Lymphedema (congenital)</term><term>Lymphedema (etiology)</term><term>Male</term><term>Middle Aged</term><term>Stewart-Treves syndrome</term><term>angiosarcoma</term><term>breast carcinoma</term><term>lymphangiosarcoma</term><term>lymphedema</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adulte d'âge moyen</term><term>Association thérapeutique (effets indésirables)</term><term>Femelle</term><term>Humains</term><term>Lymphangiosarcome ()</term><term>Lymphangiosarcome (diagnostic)</term><term>Lymphangiosarcome (étiologie)</term><term>Lymphoedème ()</term><term>Lymphoedème (étiologie)</term><term>Mâle</term><term>Sujet âgé</term><term>Tumeurs du sein ()</term></keywords><keywords scheme="MESH" qualifier="adverse effects" xml:lang="en"><term>Combined Modality Therapy</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Breast Neoplasms</term><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Lymphangiosarcoma</term></keywords><keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Lymphangiosarcome</term></keywords><keywords scheme="MESH" qualifier="effets indésirables" xml:lang="fr"><term>Association thérapeutique</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Lymphangiosarcoma</term><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Breast Neoplasms</term><term>Lymphangiosarcoma</term></keywords><keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Lymphangiosarcome</term><term>Lymphoedème</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Adulte d'âge moyen</term><term>Complication</term><term>Femelle</term><term>Homme</term><term>Humains</term><term>Lymphangiosarcome</term><term>Lymphoedème</term><term>Mâle</term><term>Sujet âgé</term><term>Tumeurs du sein</term></keywords><keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">A series of eight patients with chronic lymphedema-related lymphangiosarcoma is presented. All but one case showed a typical rapid progression and fatal outcome, as has been reported in other series. In one patient the lymphangiosarcoma developed on the chest wall, the axilla and the arm where persisting lymphedema and fibrosis occurred after bilateral mastectomy and bilateral postoperative radiotherapy. In this patient an asymptomatic course and slow locoregional progression of lesions was seen. The clinical picture, the etiological considerations and the therapeutic options of the lymphedema-induced lymphangiosarcoma with regard to the literature are discussed.</div></front></TEI><affiliations><list><country><li>Pays-Bas</li></country><region><li>Hollande-Septentrionale</li></region><settlement><li>Amsterdam</li></settlement></list><tree><country name="Pays-Bas"><region name="Hollande-Septentrionale"><name sortKey="Janse, Arieke J" sort="Janse, Arieke J" uniqKey="Janse A" first="Arieke J." last="Janse">Arieke J. Janse</name></region><name sortKey="Coevorden, Frits Van" sort="Coevorden, Frits Van" uniqKey="Coevorden F" first="Frits Van" last="Coevorden">Frits Van Coevorden</name><name sortKey="Dongen, Johannes A Van" sort="Dongen, Johannes A Van" uniqKey="Dongen J" first="Johannes A. Van" last="Dongen">Johannes A. Van Dongen</name><name sortKey="Keus, Ronald B" sort="Keus, Ronald B" uniqKey="Keus R" first="Ronald B." last="Keus">Ronald B. Keus</name><name sortKey="Peterse, Hans" sort="Peterse, Hans" uniqKey="Peterse H" first="Hans" last="Peterse">Hans Peterse</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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