Serveur d'exploration sur le lymphœdème

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[Primary cutaneous monomelic B-cell lymphoma].

Identifieur interne : 005049 ( PubMed/Curation ); précédent : 005048; suivant : 005050

[Primary cutaneous monomelic B-cell lymphoma].

Auteurs : C. Marquart-Elbaz ; D. Lipsker ; B. Cribier ; M. Meyer ; E. Heid

Source :

RBID : pubmed:9739929

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English descriptors

Abstract

Cutaneous B cell lymphomas, especially when appearing as a monomelic papulonodular eruption, are rare.

PubMed: 9739929

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C. Marquart-Elbaz
<affiliation>
<nlm:affiliation>Clinique Dermatologique, des Hôpitaux Universitaires de Strasbourg.</nlm:affiliation>
<wicri:noCountry code="subField">des Hôpitaux Universitaires de Strasbourg</wicri:noCountry>
</affiliation>

Le document en format XML

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<title xml:lang="en">[Primary cutaneous monomelic B-cell lymphoma].</title>
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<name sortKey="Marquart Elbaz, C" sort="Marquart Elbaz, C" uniqKey="Marquart Elbaz C" first="C" last="Marquart-Elbaz">C. Marquart-Elbaz</name>
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<nlm:affiliation>Clinique Dermatologique, des Hôpitaux Universitaires de Strasbourg.</nlm:affiliation>
<wicri:noCountry code="subField">des Hôpitaux Universitaires de Strasbourg</wicri:noCountry>
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<name sortKey="Lipsker, D" sort="Lipsker, D" uniqKey="Lipsker D" first="D" last="Lipsker">D. Lipsker</name>
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<name sortKey="Cribier, B" sort="Cribier, B" uniqKey="Cribier B" first="B" last="Cribier">B. Cribier</name>
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<name sortKey="Meyer, M" sort="Meyer, M" uniqKey="Meyer M" first="M" last="Meyer">M. Meyer</name>
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<name sortKey="Heid, E" sort="Heid, E" uniqKey="Heid E" first="E" last="Heid">E. Heid</name>
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<title xml:lang="en">[Primary cutaneous monomelic B-cell lymphoma].</title>
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<series>
<title level="j">Annales de dermatologie et de venereologie</title>
<idno type="ISSN">0151-9638</idno>
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<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Female</term>
<term>Humans</term>
<term>Immunohistochemistry</term>
<term>Leg</term>
<term>Lymphedema (complications)</term>
<term>Lymphoma, B-Cell (pathology)</term>
<term>Lymphoma, B-Cell (radiotherapy)</term>
<term>Neoplasms, Second Primary</term>
<term>Skin Neoplasms (pathology)</term>
<term>Skin Neoplasms (radiotherapy)</term>
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<keywords scheme="KwdFr" xml:lang="fr">
<term>Femelle</term>
<term>Humains</term>
<term>Immunohistochimie</term>
<term>Jambe</term>
<term>Lymphoedème ()</term>
<term>Lymphome B (anatomopathologie)</term>
<term>Lymphome B (radiothérapie)</term>
<term>Seconde tumeur primitive</term>
<term>Sujet âgé</term>
<term>Sujet âgé de 80 ans ou plus</term>
<term>Tumeurs cutanées (anatomopathologie)</term>
<term>Tumeurs cutanées (radiothérapie)</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr">
<term>Lymphome B</term>
<term>Tumeurs cutanées</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en">
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Lymphoma, B-Cell</term>
<term>Skin Neoplasms</term>
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<keywords scheme="MESH" qualifier="radiotherapy" xml:lang="en">
<term>Lymphoma, B-Cell</term>
<term>Skin Neoplasms</term>
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<keywords scheme="MESH" qualifier="radiothérapie" xml:lang="fr">
<term>Lymphome B</term>
<term>Tumeurs cutanées</term>
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<term>Aged, 80 and over</term>
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<term>Jambe</term>
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<term>Seconde tumeur primitive</term>
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<front>
<div type="abstract" xml:lang="en">Cutaneous B cell lymphomas, especially when appearing as a monomelic papulonodular eruption, are rare.</div>
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<Issue>9</Issue>
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<Title>Annales de dermatologie et de venereologie</Title>
<ISOAbbreviation>Ann Dermatol Venereol</ISOAbbreviation>
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<ArticleTitle>[Primary cutaneous monomelic B-cell lymphoma].</ArticleTitle>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Cutaneous B cell lymphomas, especially when appearing as a monomelic papulonodular eruption, are rare.</AbstractText>
<AbstractText Label="PATIENT" NlmCategory="METHODS">Ms H. 87-year-old, consulted for a papulonodular eruption of the left lower limb which developed during the past 5 months. This limb had been the site of a lymphedema since a traumatism 8 years ago. Histopathological analysis and immunostaining of a nodule showed that it was a large cell lymphoma of follicular stem cells. There was no extracutaneous involvement and the patient was successfully treated with radiotherapy. Two months after the completed radiotherapy a cutaneous relapse on the trunk and the upper limbs was treated with cyclophosphamide-vincristine-prednisone chemotherapy.</AbstractText>
<AbstractText Label="DISCUSSION" NlmCategory="CONCLUSIONS">Lymphedema probably played a role in the genesis of this lymphoma presumably by reducing the local immune response. It may have harmed endothelial cells and maintained an antigenic stimulation leading first to lymphocyte hyperplasia and eventually to a true lymphoma, in the same way this has been proved for some MALT lymphomas.</AbstractText>
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