Histopathological and immunohistochemical features of nodular podoconiosis.
Identifieur interne : 006D17 ( Ncbi/Merge ); précédent : 006D16; suivant : 006D18Histopathological and immunohistochemical features of nodular podoconiosis.
Auteurs : Enbiale Wendemagegn [Éthiopie] ; Rajalakshmi Tirumalae ; Almut Böer-AuerSource :
- Journal of cutaneous pathology [ 1600-0560 ] ; 2015.
Descripteurs français
- KwdFr :
- Adulte, Adulte d'âge moyen, Femelle, Humains, Hyperplasie (anatomopathologie), Immunohistochimie, Jambe (anatomopathologie), Maladies rares (anatomopathologie), Maladies rares (métabolisme), Maladies rares (virologie), Maladies rares (épidémiologie), Miliaire (anatomopathologie), Mâle, Papillomaviridae (génétique), Papillomaviridae (isolement et purification), Papillome (anatomopathologie), Réaction de polymérisation en chaîne (), Sujet âgé, Éléphantiasis (anatomopathologie), Éléphantiasis (métabolisme), Éléphantiasis (virologie), Éthiopie (épidémiologie).
- MESH :
- anatomopathologie : Hyperplasie, Jambe, Maladies rares, Miliaire, Papillome, Éléphantiasis.
- génétique : Papillomaviridae.
- isolement et purification : Papillomaviridae.
- métabolisme : Maladies rares, Éléphantiasis.
- virologie : Maladies rares, Éléphantiasis.
- épidémiologie : Maladies rares, Éthiopie.
- Adulte, Adulte d'âge moyen, Femelle, Humains, Immunohistochimie, Mâle, Réaction de polymérisation en chaîne, Sujet âgé.
- Wicri :
- geographic : Éthiopie.
English descriptors
- KwdEn :
- Adult, Aged, Elephantiasis (metabolism), Elephantiasis (pathology), Elephantiasis (virology), Ethiopia (epidemiology), Female, Humans, Hyperplasia (pathology), Immunohistochemistry, Leg (pathology), Male, Middle Aged, Miliaria (pathology), Papilloma (pathology), Papillomaviridae (genetics), Papillomaviridae (isolation & purification), Polymerase Chain Reaction (methods), Rare Diseases (epidemiology), Rare Diseases (metabolism), Rare Diseases (pathology), Rare Diseases (virology).
- MESH :
- geographic , epidemiology : Ethiopia.
- epidemiology : Rare Diseases.
- genetics : Papillomaviridae.
- isolation & purification : Papillomaviridae.
- metabolism : Elephantiasis, Rare Diseases.
- methods : Polymerase Chain Reaction.
- pathology : Elephantiasis, Hyperplasia, Leg, Miliaria, Papilloma, Rare Diseases.
- virology : Elephantiasis, Rare Diseases.
- Adult, Aged, Female, Humans, Immunohistochemistry, Male, Middle Aged.
Abstract
Podoconiosis is a familial geochemical dermatosis which is common in Ethiopia but relatively unknown in Europe/United States. It is related to exposure of bare feet to volcanic soil and presents with extensive bilateral lymphedema of legs and feet. Histopathological and immunohistochemical features of it have not been described yet.
DOI: 10.1111/cup.12441
PubMed: 25401490
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pubmed:25401490Le document en format XML
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wicri:level="1"><nlm:affiliation>Federal Ministry of Health Ethiopia, Addis Abeba, Ethiopia.</nlm:affiliation><country xml:lang="fr">Éthiopie</country><wicri:regionArea>Federal Ministry of Health Ethiopia, Addis Abeba</wicri:regionArea><wicri:noRegion>Addis Abeba</wicri:noRegion></affiliation></author><author><name sortKey="Tirumalae, Rajalakshmi" sort="Tirumalae, Rajalakshmi" uniqKey="Tirumalae R" first="Rajalakshmi" last="Tirumalae">Rajalakshmi Tirumalae</name></author><author><name sortKey="Boer Auer, Almut" sort="Boer Auer, Almut" uniqKey="Boer Auer A" first="Almut" last="Böer-Auer">Almut Böer-Auer</name></author></analytic><series><title level="j">Journal of cutaneous pathology</title><idno type="eISSN">1600-0560</idno><imprint><date when="2015" type="published">2015</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Aged</term><term>Elephantiasis (metabolism)</term><term>Elephantiasis (pathology)</term><term>Elephantiasis (virology)</term><term>Ethiopia (epidemiology)</term><term>Female</term><term>Humans</term><term>Hyperplasia (pathology)</term><term>Immunohistochemistry</term><term>Leg (pathology)</term><term>Male</term><term>Middle Aged</term><term>Miliaria (pathology)</term><term>Papilloma (pathology)</term><term>Papillomaviridae (genetics)</term><term>Papillomaviridae (isolation & purification)</term><term>Polymerase Chain Reaction (methods)</term><term>Rare Diseases (epidemiology)</term><term>Rare Diseases (metabolism)</term><term>Rare Diseases (pathology)</term><term>Rare Diseases (virology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term><term>Adulte d'âge moyen</term><term>Femelle</term><term>Humains</term><term>Hyperplasie (anatomopathologie)</term><term>Immunohistochimie</term><term>Jambe (anatomopathologie)</term><term>Maladies rares (anatomopathologie)</term><term>Maladies rares (métabolisme)</term><term>Maladies rares (virologie)</term><term>Maladies rares (épidémiologie)</term><term>Miliaire (anatomopathologie)</term><term>Mâle</term><term>Papillomaviridae (génétique)</term><term>Papillomaviridae (isolement et purification)</term><term>Papillome (anatomopathologie)</term><term>Réaction de polymérisation en chaîne ()</term><term>Sujet âgé</term><term>Éléphantiasis (anatomopathologie)</term><term>Éléphantiasis (métabolisme)</term><term>Éléphantiasis (virologie)</term><term>Éthiopie (épidémiologie)</term></keywords><keywords scheme="MESH" type="geographic" qualifier="epidemiology" xml:lang="en"><term>Ethiopia</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Hyperplasie</term><term>Jambe</term><term>Maladies rares</term><term>Miliaire</term><term>Papillome</term><term>Éléphantiasis</term></keywords><keywords scheme="MESH" qualifier="epidemiology" xml:lang="en"><term>Rare Diseases</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Papillomaviridae</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Papillomaviridae</term></keywords><keywords scheme="MESH" qualifier="isolation & purification" xml:lang="en"><term>Papillomaviridae</term></keywords><keywords scheme="MESH" qualifier="isolement et purification" xml:lang="fr"><term>Papillomaviridae</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Elephantiasis</term><term>Rare Diseases</term></keywords><keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Polymerase Chain Reaction</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Maladies rares</term><term>Éléphantiasis</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Elephantiasis</term><term>Hyperplasia</term><term>Leg</term><term>Miliaria</term><term>Papilloma</term><term>Rare Diseases</term></keywords><keywords scheme="MESH" qualifier="virologie" xml:lang="fr"><term>Maladies rares</term><term>Éléphantiasis</term></keywords><keywords scheme="MESH" qualifier="virology" xml:lang="en"><term>Elephantiasis</term><term>Rare Diseases</term></keywords><keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr"><term>Maladies rares</term><term>Éthiopie</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Aged</term><term>Female</term><term>Humans</term><term>Immunohistochemistry</term><term>Male</term><term>Middle Aged</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adulte</term><term>Adulte d'âge moyen</term><term>Femelle</term><term>Humains</term><term>Immunohistochimie</term><term>Mâle</term><term>Réaction de polymérisation en chaîne</term><term>Sujet âgé</term></keywords><keywords scheme="Wicri" type="geographic" xml:lang="fr"><term>Éthiopie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Podoconiosis is a familial geochemical dermatosis which is common in Ethiopia but relatively unknown in Europe/United States. It is related to exposure of bare feet to volcanic soil and presents with extensive bilateral lymphedema of legs and feet. Histopathological and immunohistochemical features of it have not been described yet.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25401490</PMID><DateCreated><Year>2015</Year><Month>03</Month><Day>24</Day></DateCreated><DateCompleted><Year>2016</Year><Month>03</Month><Day>28</Day></DateCompleted><DateRevised><Year>2015</Year><Month>03</Month><Day>24</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1600-0560</ISSN><JournalIssue CitedMedium="Internet"><Volume>42</Volume><Issue>3</Issue><PubDate><Year>2015</Year><Month>Mar</Month></PubDate></JournalIssue><Title>Journal of cutaneous pathology</Title><ISOAbbreviation>J. Cutan. Pathol.</ISOAbbreviation></Journal><ArticleTitle>Histopathological and immunohistochemical features of nodular podoconiosis.</ArticleTitle><Pagination><MedlinePgn>173-81</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1111/cup.12441</ELocationID><Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Podoconiosis is a familial geochemical dermatosis which is common in Ethiopia but relatively unknown in Europe/United States. It is related to exposure of bare feet to volcanic soil and presents with extensive bilateral lymphedema of legs and feet. Histopathological and immunohistochemical features of it have not been described yet.</AbstractText><AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">The objectives of this study are to characterize podoconiosis histopathologically and immunohistochemically and to increase awareness of the disease.</AbstractText><AbstractText Label="METHODS" NlmCategory="METHODS">Ten specimens of fully developed podoconiosis were examined with hematoxylin/eosin, periodic acid-Schiff, Gram, elastica-van Gieson stainings, with immunohistochemistry (CD3,CD20,CD31,CD68,CD138, tryptase, podoplanin, collagen IV), and with polymerase chain reaction (PCR) for human papillomavirus (HPV)-specific DNA.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">All specimens showed verrucous acanthosis and papillomatosis. Eccrine ducts demonstrated hyperplasia, syringofibroadenomatous changes and miliaria. Dermal collagen bundles were thickened, and elastic fibers were dramatically reduced. A moderate lymphoplasmacytic infiltrate was joined by mast cells and scattered macrophages; neutrophils and eosinophils were sparse. Blood vessels were increased, dilated, and often sclerotic while lymphatics were reduced and largely not dilated. HPV-PCR was negative in all specimens.</AbstractText><AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Podoconiosis demonstrates distinctive changes of chronic lymphedema with extensive sclerosis, loss of elastic fibers, verrucous acanthosis (not HPV induced) and reactive changes of eccrine structures. Mast cells, macrophages and altered blood vessels may be involved in the pathogenesis.</AbstractText><CopyrightInformation>© 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Wendemagegn</LastName><ForeName>Enbiale</ForeName><Initials>E</Initials><AffiliationInfo><Affiliation>Federal Ministry of Health Ethiopia, Addis Abeba, Ethiopia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Tirumalae</LastName><ForeName>Rajalakshmi</ForeName><Initials>R</Initials></Author><Author ValidYN="Y"><LastName>Böer-Auer</LastName><ForeName>Almut</ForeName><Initials>A</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2015</Year><Month>02</Month><Day>05</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>J Cutan Pathol</MedlineTA><NlmUniqueID>0425124</NlmUniqueID><ISSNLinking>0303-6987</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004604" MajorTopicYN="N">Elephantiasis</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName><QualifierName UI="Q000821" MajorTopicYN="N">virology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005002" MajorTopicYN="N" Type="Geographic">Ethiopia</DescriptorName><QualifierName UI="Q000453" MajorTopicYN="N">epidemiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006965" MajorTopicYN="N">Hyperplasia</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007150" MajorTopicYN="N">Immunohistochemistry</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007866" MajorTopicYN="N">Leg</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008883" MajorTopicYN="N">Miliaria</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010212" MajorTopicYN="N">Papilloma</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D027383" MajorTopicYN="N">Papillomaviridae</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016133" MajorTopicYN="N">Polymerase Chain Reaction</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="N">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D035583" MajorTopicYN="N">Rare Diseases</DescriptorName><QualifierName UI="Q000453" MajorTopicYN="N">epidemiology</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000821" MajorTopicYN="N">virology</QualifierName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">HPV</Keyword><Keyword MajorTopicYN="N">eccrine syringofibroadenoma</Keyword><Keyword MajorTopicYN="N">histopathology</Keyword><Keyword MajorTopicYN="N">miliaria</Keyword><Keyword MajorTopicYN="N">podoconiosis</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2014</Year><Month>11</Month><Day>04</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2014</Year><Month>11</Month><Day>12</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2014</Year><Month>11</Month><Day>12</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2014</Year><Month>11</Month><Day>18</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2014</Year><Month>11</Month><Day>18</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2016</Year><Month>3</Month><Day>29</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">25401490</ArticleId><ArticleId IdType="doi">10.1111/cup.12441</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Éthiopie</li></country></list><tree><noCountry><name sortKey="Boer Auer, Almut" sort="Boer Auer, Almut" uniqKey="Boer Auer A" first="Almut" last="Böer-Auer">Almut Böer-Auer</name><name sortKey="Tirumalae, Rajalakshmi" sort="Tirumalae, Rajalakshmi" uniqKey="Tirumalae R" first="Rajalakshmi" last="Tirumalae">Rajalakshmi Tirumalae</name></noCountry><country name="Éthiopie"><noRegion><name sortKey="Wendemagegn, Enbiale" sort="Wendemagegn, Enbiale" uniqKey="Wendemagegn E" first="Enbiale" last="Wendemagegn">Enbiale Wendemagegn</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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