Pleural effusion associated with primary lymphedema: a perspective on the yellow nail syndrome.
Identifieur interne : 00A985 ( Ncbi/Merge ); précédent : 00A984; suivant : 00A986Pleural effusion associated with primary lymphedema: a perspective on the yellow nail syndrome.
Auteurs : D J Beer ; W. Pereira ; G L SniderSource :
- The American review of respiratory disease [ 0003-0805 ] ; 1978.
Descripteurs français
- KwdFr :
- MESH :
- physiopathologie : Lymphoedème, Épanchement pleural.
- Adulte, Femelle, Humains, Lymphoedème, Maladies de la peau, Ongles, Syndrome, Épanchement pleural.
English descriptors
- KwdEn :
- MESH :
- complications : Lymphedema, Pleural Effusion, Skin Diseases.
- physiopathology : Lymphedema, Pleural Effusion.
- Adult, Female, Humans, Nails, Syndrome.
Abstract
A 28-year-old woman with bilateral pleural effusions and generalized, primary lymphedema beginning with facial erysipelas at 6 years of age is presented. The pleural effusions were exudates with 250 cells per mm3, 92 per cent of which were lymphocytes. Lymphatic stasis was demonstrated by persistence of the blue dye in the dorsa of her feet 3 months after a lymphangiogram of both lower extremities, pelvis, and abdomen. Her nails were not remarkable. Our patient represents the twentieth recorded case of pleural effusion in association with primary lymphedema. Women have been afflicted more than twice as often as men, and the age of onset has varied from birth to the eighth decade. Yellow dystrophic nails may precede or follow lymphedema or the pleural effusion and have occurred in only 11 of the 20 patients.
DOI: 10.1164/arrd.1978.117.3.595
PubMed: 629489
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pubmed:629489Le document en format XML
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Pereira</name></author><author><name sortKey="Snider, G L" sort="Snider, G L" uniqKey="Snider G" first="G L" last="Snider">G L Snider</name></author></analytic><series><title level="j">The American review of respiratory disease</title><idno type="ISSN">0003-0805</idno><imprint><date when="1978" type="published">1978</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Female</term><term>Humans</term><term>Lymphedema (complications)</term><term>Lymphedema (physiopathology)</term><term>Nails</term><term>Pleural Effusion (complications)</term><term>Pleural Effusion (physiopathology)</term><term>Skin Diseases (complications)</term><term>Syndrome</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term><term>Femelle</term><term>Humains</term><term>Lymphoedème ()</term><term>Lymphoedème (physiopathologie)</term><term>Maladies de la peau ()</term><term>Ongles</term><term>Syndrome</term><term>Épanchement pleural ()</term><term>Épanchement pleural (physiopathologie)</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Lymphedema</term><term>Pleural Effusion</term><term>Skin Diseases</term></keywords><keywords scheme="MESH" qualifier="physiopathologie" xml:lang="fr"><term>Lymphoedème</term><term>Épanchement pleural</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Lymphedema</term><term>Pleural Effusion</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Female</term><term>Humans</term><term>Nails</term><term>Syndrome</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adulte</term><term>Femelle</term><term>Humains</term><term>Lymphoedème</term><term>Maladies de la peau</term><term>Ongles</term><term>Syndrome</term><term>Épanchement pleural</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">A 28-year-old woman with bilateral pleural effusions and generalized, primary lymphedema beginning with facial erysipelas at 6 years of age is presented. The pleural effusions were exudates with 250 cells per mm3, 92 per cent of which were lymphocytes. Lymphatic stasis was demonstrated by persistence of the blue dye in the dorsa of her feet 3 months after a lymphangiogram of both lower extremities, pelvis, and abdomen. Her nails were not remarkable. Our patient represents the twentieth recorded case of pleural effusion in association with primary lymphedema. Women have been afflicted more than twice as often as men, and the age of onset has varied from birth to the eighth decade. Yellow dystrophic nails may precede or follow lymphedema or the pleural effusion and have occurred in only 11 of the 20 patients.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">629489</PMID><DateCreated><Year>1978</Year><Month>04</Month><Day>26</Day></DateCreated><DateCompleted><Year>1978</Year><Month>04</Month><Day>26</Day></DateCompleted><DateRevised><Year>2006</Year><Month>11</Month><Day>15</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0003-0805</ISSN><JournalIssue CitedMedium="Print"><Volume>117</Volume><Issue>3</Issue><PubDate><Year>1978</Year><Month>Mar</Month></PubDate></JournalIssue><Title>The American review of respiratory disease</Title><ISOAbbreviation>Am. Rev. Respir. Dis.</ISOAbbreviation></Journal><ArticleTitle>Pleural effusion associated with primary lymphedema: a perspective on the yellow nail syndrome.</ArticleTitle><Pagination><MedlinePgn>595-9</MedlinePgn></Pagination><Abstract><AbstractText>A 28-year-old woman with bilateral pleural effusions and generalized, primary lymphedema beginning with facial erysipelas at 6 years of age is presented. The pleural effusions were exudates with 250 cells per mm3, 92 per cent of which were lymphocytes. Lymphatic stasis was demonstrated by persistence of the blue dye in the dorsa of her feet 3 months after a lymphangiogram of both lower extremities, pelvis, and abdomen. Her nails were not remarkable. Our patient represents the twentieth recorded case of pleural effusion in association with primary lymphedema. Women have been afflicted more than twice as often as men, and the age of onset has varied from birth to the eighth decade. Yellow dystrophic nails may precede or follow lymphedema or the pleural effusion and have occurred in only 11 of the 20 patients.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Beer</LastName><ForeName>D J</ForeName><Initials>DJ</Initials></Author><Author ValidYN="Y"><LastName>Pereira</LastName><ForeName>W</ForeName><Initials>W</Initials><Suffix>Jr</Suffix></Author><Author ValidYN="Y"><LastName>Snider</LastName><ForeName>G L</ForeName><Initials>GL</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013487">Research Support, U.S. Gov't, P.H.S.</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Am Rev Respir Dis</MedlineTA><NlmUniqueID>0370523</NlmUniqueID><ISSNLinking>0003-0805</ISSNLinking></MedlineJournalInfo><CitationSubset>AIM</CitationSubset><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D009262" MajorTopicYN="N">Nails</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010996" MajorTopicYN="N">Pleural Effusion</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012871" MajorTopicYN="N">Skin Diseases</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013577" MajorTopicYN="N">Syndrome</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1978</Year><Month>3</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2001</Year><Month>3</Month><Day>28</Day><Hour>10</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1978</Year><Month>3</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">629489</ArticleId><ArticleId IdType="doi">10.1164/arrd.1978.117.3.595</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list></list><tree><noCountry><name sortKey="Beer, D J" sort="Beer, D J" uniqKey="Beer D" first="D J" last="Beer">D J Beer</name><name sortKey="Pereira, W" sort="Pereira, W" uniqKey="Pereira W" first="W" last="Pereira">W. 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