Yellow nail syndrome.
Identifieur interne : 002D95 ( PubMed/Checkpoint ); précédent : 002D94; suivant : 002D96Yellow nail syndrome.
Auteurs : Sarina B. Elmariah [États-Unis] ; Ravi R. Ubriani ; Olympia KovichSource :
- Dermatology online journal [ 1087-2108 ] ; 2008.
Descripteurs français
- KwdFr :
- Bronchite (étiologie), Doigts, Erreurs de diagnostic, Humains, Mâle, Oedème (étiologie), Ongles malformés (diagnostic), Ongles malformés (étiologie), Onychomycose (diagnostic), Onychopathies (diagnostic), Onychopathies (étiologie), Orteils, Sinusite (étiologie), Sujet âgé, Syndrome, Toux (étiologie).
- MESH :
- diagnostic : Ongles malformés, Onychomycose, Onychopathies.
- étiologie : Bronchite, Oedème, Ongles malformés, Onychopathies, Sinusite, Toux.
- Doigts, Erreurs de diagnostic, Humains, Mâle, Orteils, Sujet âgé, Syndrome.
English descriptors
- KwdEn :
- MESH :
- diagnosis : Nail Diseases, Nails, Malformed, Onychomycosis.
- etiology : Bronchitis, Cough, Edema, Nail Diseases, Nails, Malformed, Sinusitis.
- Aged, Diagnostic Errors, Fingers, Humans, Male, Syndrome, Toes.
Abstract
A 70-year-old man presented with a three-year history of thickened and slow growing, yellow-to-green, discolored fingernails and toenails with loss of lunulae and cuticles. He also had a concurrent history of chronic sinusitis with persistent productive cough. His presentation was consistent with the diagnosis of yellow nail syndrome (YNS), which is a rare disorder classically characterized by the triad of yellow dystrophic nails, lymphedema, and respiratory tract abnormalities but which more frequently manifests with only two of three features. The exact mechanism of YNS remains unknown; however, it is thought to reflect functional and/or anatomic defects in the lymphatic vasculature. Treatment options are limited and often unsuccessful, but spontaneous remission occurs in approximately 30 percent of affected patients.
PubMed: 19061616
Affiliations:
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pubmed:19061616Le document en format XML
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<author><name sortKey="Elmariah, Sarina B" sort="Elmariah, Sarina B" uniqKey="Elmariah S" first="Sarina B" last="Elmariah">Sarina B. Elmariah</name>
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<wicri:regionArea>Department of Dermatology, New York University</wicri:regionArea>
<wicri:noRegion>New York University</wicri:noRegion>
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<term>Fingers</term>
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<term>Ongles malformés (diagnostic)</term>
<term>Ongles malformés (étiologie)</term>
<term>Onychomycose (diagnostic)</term>
<term>Onychopathies (diagnostic)</term>
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<term>Nails, Malformed</term>
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<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Bronchite</term>
<term>Oedème</term>
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<front><div type="abstract" xml:lang="en">A 70-year-old man presented with a three-year history of thickened and slow growing, yellow-to-green, discolored fingernails and toenails with loss of lunulae and cuticles. He also had a concurrent history of chronic sinusitis with persistent productive cough. His presentation was consistent with the diagnosis of yellow nail syndrome (YNS), which is a rare disorder classically characterized by the triad of yellow dystrophic nails, lymphedema, and respiratory tract abnormalities but which more frequently manifests with only two of three features. The exact mechanism of YNS remains unknown; however, it is thought to reflect functional and/or anatomic defects in the lymphatic vasculature. Treatment options are limited and often unsuccessful, but spontaneous remission occurs in approximately 30 percent of affected patients.</div>
</front>
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<Title>Dermatology online journal</Title>
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<Abstract><AbstractText>A 70-year-old man presented with a three-year history of thickened and slow growing, yellow-to-green, discolored fingernails and toenails with loss of lunulae and cuticles. He also had a concurrent history of chronic sinusitis with persistent productive cough. His presentation was consistent with the diagnosis of yellow nail syndrome (YNS), which is a rare disorder classically characterized by the triad of yellow dystrophic nails, lymphedema, and respiratory tract abnormalities but which more frequently manifests with only two of three features. The exact mechanism of YNS remains unknown; however, it is thought to reflect functional and/or anatomic defects in the lymphatic vasculature. Treatment options are limited and often unsuccessful, but spontaneous remission occurs in approximately 30 percent of affected patients.</AbstractText>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Elmariah</LastName>
<ForeName>Sarina B</ForeName>
<Initials>SB</Initials>
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<country name="États-Unis"><noRegion><name sortKey="Elmariah, Sarina B" sort="Elmariah, Sarina B" uniqKey="Elmariah S" first="Sarina B" last="Elmariah">Sarina B. Elmariah</name>
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