Lymphangiosarcoma in chronic hereditary oedema (Milroy's disease).
Identifieur interne : 00DE37 ( Main/Exploration ); précédent : 00DE36; suivant : 00DE38Lymphangiosarcoma in chronic hereditary oedema (Milroy's disease).
Auteurs : L A Broström [Suède] ; U. Nilsonne ; M. Kronberg ; G. SöderbergSource :
- Annales chirurgiae et gynaecologiae [ 0355-9521 ] ; 1989.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- complications : Lymphangiosarcoma, Lymphedema, Soft Tissue Neoplasms.
- congenital : Lymphedema.
- Adult, Arm, Child, Female, Humans, Leg.
Abstract
Lymphangiosarcoma arising in chronic lymphoedema is extremely rare. In a reference population of about four million people, during a thirty year period (1957-1987), only four patients were treated for such a tumour. The neoplasm is almost exclusively seen in elderly patients after mastectomy but in two of our patients, reported in this paper, it arose in chronic hereditary oedema (Milroy's disease). In both these patients there was a considerable treatment delay because of wrong diagnosis. The tumour extent was difficult to assess macroscopically and ablative surgery had to be a disarticulation of the involved extremity. Macular or papular purple lesions in a lymphoedematous extremity should be a manifestation of this aggressive neoplasm.
PubMed: 2624407
Affiliations:
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Le document en format XML
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<author><name sortKey="Kronberg, M" sort="Kronberg, M" uniqKey="Kronberg M" first="M" last="Kronberg">M. Kronberg</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Lymphangiosarcoma in chronic hereditary oedema (Milroy's disease).</title>
<author><name sortKey="Brostrom, L A" sort="Brostrom, L A" uniqKey="Brostrom L" first="L A" last="Broström">L A Broström</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Orthopaedics, Karolinska Hospital and Institute, Stockholm, Sweden.</nlm:affiliation>
<country xml:lang="fr">Suède</country>
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<author><name sortKey="Nilsonne, U" sort="Nilsonne, U" uniqKey="Nilsonne U" first="U" last="Nilsonne">U. Nilsonne</name>
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<author><name sortKey="Kronberg, M" sort="Kronberg, M" uniqKey="Kronberg M" first="M" last="Kronberg">M. Kronberg</name>
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<author><name sortKey="Soderberg, G" sort="Soderberg, G" uniqKey="Soderberg G" first="G" last="Söderberg">G. Söderberg</name>
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<series><title level="j">Annales chirurgiae et gynaecologiae</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Arm</term>
<term>Child</term>
<term>Female</term>
<term>Humans</term>
<term>Leg</term>
<term>Lymphangiosarcoma (complications)</term>
<term>Lymphedema (complications)</term>
<term>Lymphedema (congenital)</term>
<term>Soft Tissue Neoplasms (complications)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term>
<term>Bras</term>
<term>Enfant</term>
<term>Femelle</term>
<term>Humains</term>
<term>Jambe</term>
<term>Lymphangiosarcome ()</term>
<term>Lymphoedème ()</term>
<term>Tumeurs des tissus mous ()</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Lymphangiosarcoma</term>
<term>Lymphedema</term>
<term>Soft Tissue Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Arm</term>
<term>Child</term>
<term>Female</term>
<term>Humans</term>
<term>Leg</term>
</keywords>
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<term>Bras</term>
<term>Enfant</term>
<term>Femelle</term>
<term>Humains</term>
<term>Jambe</term>
<term>Lymphangiosarcome</term>
<term>Lymphoedème</term>
<term>Tumeurs des tissus mous</term>
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<front><div type="abstract" xml:lang="en">Lymphangiosarcoma arising in chronic lymphoedema is extremely rare. In a reference population of about four million people, during a thirty year period (1957-1987), only four patients were treated for such a tumour. The neoplasm is almost exclusively seen in elderly patients after mastectomy but in two of our patients, reported in this paper, it arose in chronic hereditary oedema (Milroy's disease). In both these patients there was a considerable treatment delay because of wrong diagnosis. The tumour extent was difficult to assess macroscopically and ablative surgery had to be a disarticulation of the involved extremity. Macular or papular purple lesions in a lymphoedematous extremity should be a manifestation of this aggressive neoplasm.</div>
</front>
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<tree><noCountry><name sortKey="Kronberg, M" sort="Kronberg, M" uniqKey="Kronberg M" first="M" last="Kronberg">M. Kronberg</name>
<name sortKey="Nilsonne, U" sort="Nilsonne, U" uniqKey="Nilsonne U" first="U" last="Nilsonne">U. Nilsonne</name>
<name sortKey="Soderberg, G" sort="Soderberg, G" uniqKey="Soderberg G" first="G" last="Söderberg">G. Söderberg</name>
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<country name="Suède"><region name="Svealand"><name sortKey="Brostrom, L A" sort="Brostrom, L A" uniqKey="Brostrom L" first="L A" last="Broström">L A Broström</name>
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