A case of primary cutaneous nasal type NK/T-cell lymphoma and review of the literature
Identifieur interne : 000497 ( PascalFrancis/Corpus ); précédent : 000496; suivant : 000498A case of primary cutaneous nasal type NK/T-cell lymphoma and review of the literature
Auteurs : J. Stokkermans-Dubois ; T. Jouary ; B. Vergier ; M. M. Delaunay ; A. TaiebSource :
- Dermatology : (Basel) [ 1018-8665 ] ; 2006.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
Introduction: Cutaneous T-cell lymphoma subtypes are now better identified thanks to progress in immunohistochemistry. This article describes a new case of primary cutaneous natural killer/T-cell lymphoma of nasal type (NKTL-NT) and reviews 18 other cases of this rare neoplasm. Case Report: A 79-year-old man presented with a 3-cm nodular tumor of the left leg occurring on a primary chronic lymphedema of the legs. The lesion was CD56+, CD3 intracytoplasmic+, CD45+ and Epstein-Barr virus+. A comprehensive workup including CTscan and bone marrow biopsy was negative and a diagnosis of NKTL-NT with a primary cutaneous involvement was made. The patient was free of disease under multi-agent chemotherapy after 24 months of follow-up. Discussion: After reviewing 18 other cases of primary cutaneous NKTL-NT, we conclude that the prognosis of these lymphomas is usually poor. However, limited cutaneous forms have a longer median survival than extracutaneous variants.
Notice en format standard (ISO 2709)
Pour connaître la documentation sur le format Inist Standard.
pA |
|
---|
Format Inist (serveur)
NO : | PASCAL 07-0047696 INIST |
---|---|
ET : | A case of primary cutaneous nasal type NK/T-cell lymphoma and review of the literature |
AU : | STOKKERMANS-DUBOIS (J.); JOUARY (T.); VERGIER (B.); DELAUNAY (M. M.); TAIEB (A.) |
AF : | Skin and Cancer Unit, Department of Dermatology, Saint André Hospital/Bordeaux/France (1 aut., 2 aut., 4 aut., 5 aut.); Department of Pathology, Haut-Lévêque Hospital/Pessac/France (3 aut.) |
DT : | Publication en série; Etude de cas, cas et faits cliniques; Niveau analytique |
SO : | Dermatology : (Basel); ISSN 1018-8665; Suisse; Da. 2006; Vol. 213; No. 4; Pp. 345-349; Bibl. 12 ref. |
LA : | Anglais |
EA : | Introduction: Cutaneous T-cell lymphoma subtypes are now better identified thanks to progress in immunohistochemistry. This article describes a new case of primary cutaneous natural killer/T-cell lymphoma of nasal type (NKTL-NT) and reviews 18 other cases of this rare neoplasm. Case Report: A 79-year-old man presented with a 3-cm nodular tumor of the left leg occurring on a primary chronic lymphedema of the legs. The lesion was CD56+, CD3 intracytoplasmic+, CD45+ and Epstein-Barr virus+. A comprehensive workup including CTscan and bone marrow biopsy was negative and a diagnosis of NKTL-NT with a primary cutaneous involvement was made. The patient was free of disease under multi-agent chemotherapy after 24 months of follow-up. Discussion: After reviewing 18 other cases of primary cutaneous NKTL-NT, we conclude that the prognosis of these lymphomas is usually poor. However, limited cutaneous forms have a longer median survival than extracutaneous variants. |
CC : | 002B08; 002B19B; 002B06D01 |
FD : | Lymphome; Immunodéficit; Lymphoedème; Primaire; Peau; Nez; Cellule NK; Lymphocyte T; Article synthèse; Dermatologie |
FG : | Hémopathie maligne; Lymphoprolifératif syndrome; Immunopathologie; Appareil circulatoire pathologie; Lymphatique pathologie |
ED : | Lymphoma; Immune deficiency; Lymphedema; Primary; Skin; Nose; Natural killer cell; T-Lymphocyte; Review; Dermatology |
EG : | Malignant hemopathy; Lymphoproliferative syndrome; Immunopathology; Cardiovascular disease; Lymphatic vessel disease |
SD : | Linfoma; Inmunodeficiencia; Linfedema; Primario; Piel; Nariz; Célula NK; Linfocito T; Artículo síntesis; Dermatología |
LO : | INIST-4530.354000145098490140 |
ID : | 07-0047696 |
Links to Exploration step
Pascal:07-0047696Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">A case of primary cutaneous nasal type NK/T-cell lymphoma and review of the literature</title>
<author><name sortKey="Stokkermans Dubois, J" sort="Stokkermans Dubois, J" uniqKey="Stokkermans Dubois J" first="J." last="Stokkermans-Dubois">J. Stokkermans-Dubois</name>
<affiliation><inist:fA14 i1="01"><s1>Skin and Cancer Unit, Department of Dermatology, Saint André Hospital</s1>
<s2>Bordeaux</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Jouary, T" sort="Jouary, T" uniqKey="Jouary T" first="T." last="Jouary">T. Jouary</name>
<affiliation><inist:fA14 i1="01"><s1>Skin and Cancer Unit, Department of Dermatology, Saint André Hospital</s1>
<s2>Bordeaux</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Vergier, B" sort="Vergier, B" uniqKey="Vergier B" first="B." last="Vergier">B. Vergier</name>
<affiliation><inist:fA14 i1="02"><s1>Department of Pathology, Haut-Lévêque Hospital</s1>
<s2>Pessac</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Delaunay, M M" sort="Delaunay, M M" uniqKey="Delaunay M" first="M. M." last="Delaunay">M. M. Delaunay</name>
<affiliation><inist:fA14 i1="01"><s1>Skin and Cancer Unit, Department of Dermatology, Saint André Hospital</s1>
<s2>Bordeaux</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Taieb, A" sort="Taieb, A" uniqKey="Taieb A" first="A." last="Taieb">A. Taieb</name>
<affiliation><inist:fA14 i1="01"><s1>Skin and Cancer Unit, Department of Dermatology, Saint André Hospital</s1>
<s2>Bordeaux</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">07-0047696</idno>
<date when="2006">2006</date>
<idno type="stanalyst">PASCAL 07-0047696 INIST</idno>
<idno type="RBID">Pascal:07-0047696</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000497</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">A case of primary cutaneous nasal type NK/T-cell lymphoma and review of the literature</title>
<author><name sortKey="Stokkermans Dubois, J" sort="Stokkermans Dubois, J" uniqKey="Stokkermans Dubois J" first="J." last="Stokkermans-Dubois">J. Stokkermans-Dubois</name>
<affiliation><inist:fA14 i1="01"><s1>Skin and Cancer Unit, Department of Dermatology, Saint André Hospital</s1>
<s2>Bordeaux</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Jouary, T" sort="Jouary, T" uniqKey="Jouary T" first="T." last="Jouary">T. Jouary</name>
<affiliation><inist:fA14 i1="01"><s1>Skin and Cancer Unit, Department of Dermatology, Saint André Hospital</s1>
<s2>Bordeaux</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Vergier, B" sort="Vergier, B" uniqKey="Vergier B" first="B." last="Vergier">B. Vergier</name>
<affiliation><inist:fA14 i1="02"><s1>Department of Pathology, Haut-Lévêque Hospital</s1>
<s2>Pessac</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Delaunay, M M" sort="Delaunay, M M" uniqKey="Delaunay M" first="M. M." last="Delaunay">M. M. Delaunay</name>
<affiliation><inist:fA14 i1="01"><s1>Skin and Cancer Unit, Department of Dermatology, Saint André Hospital</s1>
<s2>Bordeaux</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Taieb, A" sort="Taieb, A" uniqKey="Taieb A" first="A." last="Taieb">A. Taieb</name>
<affiliation><inist:fA14 i1="01"><s1>Skin and Cancer Unit, Department of Dermatology, Saint André Hospital</s1>
<s2>Bordeaux</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</analytic>
<series><title level="j" type="main">Dermatology : (Basel)</title>
<title level="j" type="abbreviated">Dermatology : (Basel)</title>
<idno type="ISSN">1018-8665</idno>
<imprint><date when="2006">2006</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">Dermatology : (Basel)</title>
<title level="j" type="abbreviated">Dermatology : (Basel)</title>
<idno type="ISSN">1018-8665</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Dermatology</term>
<term>Immune deficiency</term>
<term>Lymphedema</term>
<term>Lymphoma</term>
<term>Natural killer cell</term>
<term>Nose</term>
<term>Primary</term>
<term>Review</term>
<term>Skin</term>
<term>T-Lymphocyte</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Lymphome</term>
<term>Immunodéficit</term>
<term>Lymphoedème</term>
<term>Primaire</term>
<term>Peau</term>
<term>Nez</term>
<term>Cellule NK</term>
<term>Lymphocyte T</term>
<term>Article synthèse</term>
<term>Dermatologie</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Introduction: Cutaneous T-cell lymphoma subtypes are now better identified thanks to progress in immunohistochemistry. This article describes a new case of primary cutaneous natural killer/T-cell lymphoma of nasal type (NKTL-NT) and reviews 18 other cases of this rare neoplasm. Case Report: A 79-year-old man presented with a 3-cm nodular tumor of the left leg occurring on a primary chronic lymphedema of the legs. The lesion was CD56+, CD3 intracytoplasmic+, CD45+ and Epstein-Barr virus+. A comprehensive workup including CTscan and bone marrow biopsy was negative and a diagnosis of NKTL-NT with a primary cutaneous involvement was made. The patient was free of disease under multi-agent chemotherapy after 24 months of follow-up. Discussion: After reviewing 18 other cases of primary cutaneous NKTL-NT, we conclude that the prognosis of these lymphomas is usually poor. However, limited cutaneous forms have a longer median survival than extracutaneous variants.</div>
</front>
</TEI>
<inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1018-8665</s0>
</fA01>
<fA03 i2="1"><s0>Dermatology : (Basel)</s0>
</fA03>
<fA05><s2>213</s2>
</fA05>
<fA06><s2>4</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG"><s1>A case of primary cutaneous nasal type NK/T-cell lymphoma and review of the literature</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>STOKKERMANS-DUBOIS (J.)</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>JOUARY (T.)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>VERGIER (B.)</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>DELAUNAY (M. M.)</s1>
</fA11>
<fA11 i1="05" i2="1"><s1>TAIEB (A.)</s1>
</fA11>
<fA14 i1="01"><s1>Skin and Cancer Unit, Department of Dermatology, Saint André Hospital</s1>
<s2>Bordeaux</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Department of Pathology, Haut-Lévêque Hospital</s1>
<s2>Pessac</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</fA14>
<fA20><s1>345-349</s1>
</fA20>
<fA21><s1>2006</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
<fA43 i1="01"><s1>INIST</s1>
<s2>4530</s2>
<s5>354000145098490140</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2007 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>12 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>07-0047696</s0>
</fA47>
<fA60><s1>P</s1>
<s3>EC</s3>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>Dermatology : (Basel)</s0>
</fA64>
<fA66 i1="01"><s0>CHE</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>Introduction: Cutaneous T-cell lymphoma subtypes are now better identified thanks to progress in immunohistochemistry. This article describes a new case of primary cutaneous natural killer/T-cell lymphoma of nasal type (NKTL-NT) and reviews 18 other cases of this rare neoplasm. Case Report: A 79-year-old man presented with a 3-cm nodular tumor of the left leg occurring on a primary chronic lymphedema of the legs. The lesion was CD56+, CD3 intracytoplasmic+, CD45+ and Epstein-Barr virus+. A comprehensive workup including CTscan and bone marrow biopsy was negative and a diagnosis of NKTL-NT with a primary cutaneous involvement was made. The patient was free of disease under multi-agent chemotherapy after 24 months of follow-up. Discussion: After reviewing 18 other cases of primary cutaneous NKTL-NT, we conclude that the prognosis of these lymphomas is usually poor. However, limited cutaneous forms have a longer median survival than extracutaneous variants.</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>002B08</s0>
</fC02>
<fC02 i1="02" i2="X"><s0>002B19B</s0>
</fC02>
<fC02 i1="03" i2="X"><s0>002B06D01</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE"><s0>Lymphome</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG"><s0>Lymphoma</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Linfoma</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE"><s0>Immunodéficit</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Immune deficiency</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Inmunodeficiencia</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Lymphoedème</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Lymphedema</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Linfedema</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Primaire</s0>
<s5>09</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Primary</s0>
<s5>09</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Primario</s0>
<s5>09</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Peau</s0>
<s5>10</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Skin</s0>
<s5>10</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Piel</s0>
<s5>10</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Nez</s0>
<s5>11</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Nose</s0>
<s5>11</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Nariz</s0>
<s5>11</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Cellule NK</s0>
<s5>12</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Natural killer cell</s0>
<s5>12</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Célula NK</s0>
<s5>12</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE"><s0>Lymphocyte T</s0>
<s5>13</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG"><s0>T-Lymphocyte</s0>
<s5>13</s5>
<s6>«T»-Lymphocyte</s6>
</fC03>
<fC03 i1="08" i2="X" l="SPA"><s0>Linfocito T</s0>
<s5>13</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE"><s0>Article synthèse</s0>
<s5>14</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG"><s0>Review</s0>
<s5>14</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA"><s0>Artículo síntesis</s0>
<s5>14</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE"><s0>Dermatologie</s0>
<s5>15</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG"><s0>Dermatology</s0>
<s5>15</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA"><s0>Dermatología</s0>
<s5>15</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Hémopathie maligne</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Malignant hemopathy</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Hemopatía maligna</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Lymphoprolifératif syndrome</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Lymphoproliferative syndrome</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Linfoproliferativo síndrome</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Immunopathologie</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Immunopathology</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Inmunopatología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Appareil circulatoire pathologie</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Cardiovascular disease</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Aparato circulatorio patología</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Lymphatique pathologie</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Lymphatic vessel disease</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Linfático patología</s0>
<s5>41</s5>
</fC07>
<fN21><s1>029</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
<server><NO>PASCAL 07-0047696 INIST</NO>
<ET>A case of primary cutaneous nasal type NK/T-cell lymphoma and review of the literature</ET>
<AU>STOKKERMANS-DUBOIS (J.); JOUARY (T.); VERGIER (B.); DELAUNAY (M. M.); TAIEB (A.)</AU>
<AF>Skin and Cancer Unit, Department of Dermatology, Saint André Hospital/Bordeaux/France (1 aut., 2 aut., 4 aut., 5 aut.); Department of Pathology, Haut-Lévêque Hospital/Pessac/France (3 aut.)</AF>
<DT>Publication en série; Etude de cas, cas et faits cliniques; Niveau analytique</DT>
<SO>Dermatology : (Basel); ISSN 1018-8665; Suisse; Da. 2006; Vol. 213; No. 4; Pp. 345-349; Bibl. 12 ref.</SO>
<LA>Anglais</LA>
<EA>Introduction: Cutaneous T-cell lymphoma subtypes are now better identified thanks to progress in immunohistochemistry. This article describes a new case of primary cutaneous natural killer/T-cell lymphoma of nasal type (NKTL-NT) and reviews 18 other cases of this rare neoplasm. Case Report: A 79-year-old man presented with a 3-cm nodular tumor of the left leg occurring on a primary chronic lymphedema of the legs. The lesion was CD56+, CD3 intracytoplasmic+, CD45+ and Epstein-Barr virus+. A comprehensive workup including CTscan and bone marrow biopsy was negative and a diagnosis of NKTL-NT with a primary cutaneous involvement was made. The patient was free of disease under multi-agent chemotherapy after 24 months of follow-up. Discussion: After reviewing 18 other cases of primary cutaneous NKTL-NT, we conclude that the prognosis of these lymphomas is usually poor. However, limited cutaneous forms have a longer median survival than extracutaneous variants.</EA>
<CC>002B08; 002B19B; 002B06D01</CC>
<FD>Lymphome; Immunodéficit; Lymphoedème; Primaire; Peau; Nez; Cellule NK; Lymphocyte T; Article synthèse; Dermatologie</FD>
<FG>Hémopathie maligne; Lymphoprolifératif syndrome; Immunopathologie; Appareil circulatoire pathologie; Lymphatique pathologie</FG>
<ED>Lymphoma; Immune deficiency; Lymphedema; Primary; Skin; Nose; Natural killer cell; T-Lymphocyte; Review; Dermatology</ED>
<EG>Malignant hemopathy; Lymphoproliferative syndrome; Immunopathology; Cardiovascular disease; Lymphatic vessel disease</EG>
<SD>Linfoma; Inmunodeficiencia; Linfedema; Primario; Piel; Nariz; Célula NK; Linfocito T; Artículo síntesis; Dermatología</SD>
<LO>INIST-4530.354000145098490140</LO>
<ID>07-0047696</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 000497 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/PascalFrancis/Corpus/biblio.hfd -nk 000497 | 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:07-0047696 |texte= A case of primary cutaneous nasal type NK/T-cell lymphoma and review of the literature }}
This area was generated with Dilib version V0.6.31. |