Yellow nail syndrome: missed diagnosis of a rare syndrome.
Identifieur interne : 002221 ( PubMed/Checkpoint ); précédent : 002220; suivant : 002222Yellow nail syndrome: missed diagnosis of a rare syndrome.
Auteurs : Laxman K. Chavda ; Rama A. Vaidya ; Ashok D B. VaidyaSource :
- The Journal of the Association of Physicians of India [ 0004-5772 ] ; 2011.
Descripteurs français
- KwdFr :
- MESH :
- diagnostic : Lymphoedème, Syndrome des ongles jaunes, Épanchement pleural.
- usage thérapeutique : Talc.
- Adulte d'âge moyen, Humains, Lymphoedème, Mâle, Pleurodèse, Syndrome des ongles jaunes, Épanchement pleural.
English descriptors
- KwdEn :
- MESH :
- chemical , therapeutic use : Talc.
- complications : Lymphedema, Pleural Effusion, Yellow Nail Syndrome.
- diagnosis : Lymphedema, Pleural Effusion, Yellow Nail Syndrome.
- therapy : Pleural Effusion.
- Humans, Male, Middle Aged, Pleurodesis.
Abstract
A 61 year old male, with a bilateral persistent and recurrent pleural effusion, had undergone frequent tapping over a period of eight months, prior to the referral. The patient was treated earlier to the referral empirically for pulmonary tuberculosis with no response to the treatment. Malignancy was suspected and ruled out. A detailed examination showed that he also had atrophic nails with yellow discoloration and lymphedema of feet. Yellow nail syndrome was diagnosed on the basis of the clinical findings of the triad viz. yellow atrophic nails, lymphedema and bilateral pleural effusions. Pathogenesis still remains elusive for the syndrome. Pleurodesis provided both symptomatic relief and a respite from repeated tapping. The case is presented as a rare condition, which was missed for diagnosis, for quite some time by several specialists.
PubMed: 21755767
Affiliations:
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pubmed:21755767Le document en format XML
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The patient was treated earlier to the referral empirically for pulmonary tuberculosis with no response to the treatment. Malignancy was suspected and ruled out. A detailed examination showed that he also had atrophic nails with yellow discoloration and lymphedema of feet. Yellow nail syndrome was diagnosed on the basis of the clinical findings of the triad viz. yellow atrophic nails, lymphedema and bilateral pleural effusions. Pathogenesis still remains elusive for the syndrome. Pleurodesis provided both symptomatic relief and a respite from repeated tapping. The case is presented as a rare condition, which was missed for diagnosis, for quite some time by several specialists.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">21755767</PMID><DateCreated><Year>2011</Year><Month>07</Month><Day>15</Day></DateCreated><DateCompleted><Year>2011</Year><Month>08</Month><Day>18</Day></DateCompleted><DateRevised><Year>2011</Year><Month>07</Month><Day>15</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0004-5772</ISSN><JournalIssue CitedMedium="Print"><Volume>59</Volume><PubDate><Year>2011</Year><Month>Apr</Month></PubDate></JournalIssue><Title>The Journal of the Association of Physicians of India</Title><ISOAbbreviation>J Assoc Physicians India</ISOAbbreviation></Journal><ArticleTitle>Yellow nail syndrome: missed diagnosis of a rare syndrome.</ArticleTitle><Pagination><MedlinePgn>258-60</MedlinePgn></Pagination><Abstract><AbstractText>A 61 year old male, with a bilateral persistent and recurrent pleural effusion, had undergone frequent tapping over a period of eight months, prior to the referral. The patient was treated earlier to the referral empirically for pulmonary tuberculosis with no response to the treatment. Malignancy was suspected and ruled out. A detailed examination showed that he also had atrophic nails with yellow discoloration and lymphedema of feet. Yellow nail syndrome was diagnosed on the basis of the clinical findings of the triad viz. yellow atrophic nails, lymphedema and bilateral pleural effusions. Pathogenesis still remains elusive for the syndrome. Pleurodesis provided both symptomatic relief and a respite from repeated tapping. The case is presented as a rare condition, which was missed for diagnosis, for quite some time by several specialists.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Chavda</LastName><ForeName>Laxman K</ForeName><Initials>LK</Initials><AffiliationInfo><Affiliation>Panchanath Medical Trust, Rajkot, Gujarat.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Vaidya</LastName><ForeName>Rama A</ForeName><Initials>RA</Initials></Author><Author ValidYN="Y"><LastName>Vaidya</LastName><ForeName>Ashok D B</ForeName><Initials>AD</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>India</Country><MedlineTA>J Assoc Physicians India</MedlineTA><NlmUniqueID>7505585</NlmUniqueID><ISSNLinking>0004-5772</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>14807-96-6</RegistryNumber><NameOfSubstance UI="D013627">Talc</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName><QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010996" MajorTopicYN="N">Pleural Effusion</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName><QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName><QualifierName UI="Q000628" MajorTopicYN="Y">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018700" MajorTopicYN="N">Pleurodesis</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013627" MajorTopicYN="N">Talc</DescriptorName><QualifierName UI="Q000627" MajorTopicYN="N">therapeutic use</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D056684" MajorTopicYN="N">Yellow Nail Syndrome</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName><QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2011</Year><Month>7</Month><Day>16</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2011</Year><Month>7</Month><Day>16</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2011</Year><Month>8</Month><Day>19</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">21755767</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list></list><tree><noCountry><name sortKey="Chavda, Laxman K" sort="Chavda, Laxman K" uniqKey="Chavda L" first="Laxman K" last="Chavda">Laxman K. Chavda</name><name sortKey="Vaidya, Ashok D B" sort="Vaidya, Ashok D B" uniqKey="Vaidya A" first="Ashok D B" last="Vaidya">Ashok D B. Vaidya</name><name sortKey="Vaidya, Rama A" sort="Vaidya, Rama A" uniqKey="Vaidya R" first="Rama A" last="Vaidya">Rama A. Vaidya</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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