LymphedemaV1, PubMed, Checkpoint, bibRecord, 000840

Linear scleroderma with prominent multiple lymphadenopathy followed by the development of polymyositis: A case report and review of published work.

Identifieur interne : 000840 ( PubMed/Checkpoint ); précédent : 000839; suivant : 000841

Linear scleroderma with prominent multiple lymphadenopathy followed by the development of polymyositis: A case report and review of published work.

Auteurs : Takehiro Takahashi [Japon] ; Yoshihide Asano [Japon] ; Maiko Hirakawa [Japon] ; Kouki Nakamura [Japon] ; Ryosuke Saigusa [Japon] ; Naohiko Aozasa [Japon] ; Hayakazu Sumida [Japon] ; Hideki Fujita [Japon] ; Makoto Sugaya [Japon] ; Aki Ohmori [Japon] ; Jun Shimizu [Japon] ; Shinichi Sato [Japon]

Source :

The Journal of dermatology [ 1346-8138 ] ; 2016.

RBID : pubmed:27129435

Descripteurs français

English descriptors

KwdEn :
- Autoantibodies (blood), Autoimmune Diseases (diagnostic imaging), Autoimmune Diseases (drug therapy), Autoimmune Diseases (immunology), Autoimmune Diseases (pathology), Centrioles (immunology), Electromyography, Fascia (diagnostic imaging), Fascia (pathology), Female, Glucocorticoids (therapeutic use), Hepatomegaly (diagnostic imaging), Hepatomegaly (immunology), Humans, Lymph Nodes (pathology), Lymphadenopathy (diagnostic imaging), Lymphadenopathy (drug therapy), Lymphadenopathy (immunology), Lymphadenopathy (pathology), Lymphedema (diagnostic imaging), Lymphedema (immunology), Magnetic Resonance Imaging, Middle Aged, Muscle, Skeletal (diagnostic imaging), Muscle, Skeletal (enzymology), Muscle, Skeletal (pathology), Polymyositis (diagnostic imaging), Polymyositis (drug therapy), Polymyositis (immunology), Polymyositis (pathology), Prednisolone (therapeutic use), Scleroderma, Localized (diagnostic imaging), Scleroderma, Localized (drug therapy), Scleroderma, Localized (immunology), Scleroderma, Localized (pathology), Skin (pathology), Splenomegaly (diagnostic imaging), Splenomegaly (immunology), Tomography, X-Ray Computed.
MESH :
- chemical , blood : Autoantibodies.
- diagnostic imaging : Autoimmune Diseases, Fascia, Hepatomegaly, Lymphadenopathy, Lymphedema, Muscle, Skeletal, Polymyositis, Scleroderma, Localized, Splenomegaly.
- drug therapy : Autoimmune Diseases, Lymphadenopathy, Polymyositis, Scleroderma, Localized.
- enzymology : Muscle, Skeletal.
- immunology : Autoimmune Diseases, Centrioles, Hepatomegaly, Lymphadenopathy, Lymphedema, Polymyositis, Scleroderma, Localized, Splenomegaly.
- pathology : Autoimmune Diseases, Fascia, Lymph Nodes, Lymphadenopathy, Muscle, Skeletal, Polymyositis, Scleroderma, Localized, Skin.
- chemical , therapeutic use : Glucocorticoids, Prednisolone.
- Electromyography, Female, Humans, Magnetic Resonance Imaging, Middle Aged, Tomography, X-Ray Computed.

Abstract

Localized scleroderma is an inflammatory disorder affecting the skin and underlying tissues, a certain subset of which develops other autoimmune diseases on the basis of a prominent autoimmune background. We here report a unique case of linear scleroderma presenting with a sclerotic plaque on the left thigh, multiple lymphadenopathy in bilateral inguinal and para-aortic lymph nodes, and hepatosplenomegaly, who later developed polymyositis. We describe the detailed disease course of our case and discuss the clinical significance of multiple lymphadenopathy in localized scleroderma based on a review of published work.

DOI: 10.1111/1346-8138.13424
PubMed: 27129435

Affiliations:

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Le document en format XML

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<term>Autoimmune Diseases (diagnostic imaging)</term>
<term>Autoimmune Diseases (drug therapy)</term>
<term>Autoimmune Diseases (immunology)</term>
<term>Autoimmune Diseases (pathology)</term>
<term>Centrioles (immunology)</term>
<term>Electromyography</term>
<term>Fascia (diagnostic imaging)</term>
<term>Fascia (pathology)</term>
<term>Female</term>
<term>Glucocorticoids (therapeutic use)</term>
<term>Hepatomegaly (diagnostic imaging)</term>
<term>Hepatomegaly (immunology)</term>
<term>Humans</term>
<term>Lymph Nodes (pathology)</term>
<term>Lymphadenopathy (diagnostic imaging)</term>
<term>Lymphadenopathy (drug therapy)</term>
<term>Lymphadenopathy (immunology)</term>
<term>Lymphadenopathy (pathology)</term>
<term>Lymphedema (diagnostic imaging)</term>
<term>Lymphedema (immunology)</term>
<term>Magnetic Resonance Imaging</term>
<term>Middle Aged</term>
<term>Muscle, Skeletal (diagnostic imaging)</term>
<term>Muscle, Skeletal (enzymology)</term>
<term>Muscle, Skeletal (pathology)</term>
<term>Polymyositis (diagnostic imaging)</term>
<term>Polymyositis (drug therapy)</term>
<term>Polymyositis (immunology)</term>
<term>Polymyositis (pathology)</term>
<term>Prednisolone (therapeutic use)</term>
<term>Scleroderma, Localized (diagnostic imaging)</term>
<term>Scleroderma, Localized (drug therapy)</term>
<term>Scleroderma, Localized (immunology)</term>
<term>Scleroderma, Localized (pathology)</term>
<term>Skin (pathology)</term>
<term>Splenomegaly (diagnostic imaging)</term>
<term>Splenomegaly (immunology)</term>
<term>Tomography, X-Ray Computed</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte d'âge moyen</term>
<term>Autoanticorps (sang)</term>
<term>Centrioles (immunologie)</term>
<term>Fascia (anatomopathologie)</term>
<term>Fascia (imagerie diagnostique)</term>
<term>Femelle</term>
<term>Glucocorticoïdes (usage thérapeutique)</term>
<term>Humains</term>
<term>Hépatomégalie (imagerie diagnostique)</term>
<term>Hépatomégalie (immunologie)</term>
<term>Imagerie par résonance magnétique</term>
<term>Lymphadénopathie (anatomopathologie)</term>
<term>Lymphadénopathie (imagerie diagnostique)</term>
<term>Lymphadénopathie (immunologie)</term>
<term>Lymphadénopathie (traitement médicamenteux)</term>
<term>Lymphoedème (imagerie diagnostique)</term>
<term>Lymphoedème (immunologie)</term>
<term>Maladies auto-immunes (anatomopathologie)</term>
<term>Maladies auto-immunes (imagerie diagnostique)</term>
<term>Maladies auto-immunes (immunologie)</term>
<term>Maladies auto-immunes (traitement médicamenteux)</term>
<term>Muscles squelettiques (anatomopathologie)</term>
<term>Muscles squelettiques (enzymologie)</term>
<term>Muscles squelettiques (imagerie diagnostique)</term>
<term>Noeuds lymphatiques (anatomopathologie)</term>
<term>Peau (anatomopathologie)</term>
<term>Polymyosite (anatomopathologie)</term>
<term>Polymyosite (imagerie diagnostique)</term>
<term>Polymyosite (immunologie)</term>
<term>Polymyosite (traitement médicamenteux)</term>
<term>Prednisolone (usage thérapeutique)</term>
<term>Sclérodermie localisée (anatomopathologie)</term>
<term>Sclérodermie localisée (imagerie diagnostique)</term>
<term>Sclérodermie localisée (immunologie)</term>
<term>Sclérodermie localisée (traitement médicamenteux)</term>
<term>Splénomégalie (imagerie diagnostique)</term>
<term>Splénomégalie (immunologie)</term>
<term>Tomodensitométrie</term>
<term>Électromyographie</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en"><term>Autoantibodies</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Fascia</term>
<term>Lymphadénopathie</term>
<term>Maladies auto-immunes</term>
<term>Muscles squelettiques</term>
<term>Noeuds lymphatiques</term>
<term>Peau</term>
<term>Polymyosite</term>
<term>Sclérodermie localisée</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en"><term>Autoimmune Diseases</term>
<term>Fascia</term>
<term>Hepatomegaly</term>
<term>Lymphadenopathy</term>
<term>Lymphedema</term>
<term>Muscle, Skeletal</term>
<term>Polymyositis</term>
<term>Scleroderma, Localized</term>
<term>Splenomegaly</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Autoimmune Diseases</term>
<term>Lymphadenopathy</term>
<term>Polymyositis</term>
<term>Scleroderma, Localized</term>
</keywords>
<keywords scheme="MESH" qualifier="enzymologie" xml:lang="fr"><term>Muscles squelettiques</term>
</keywords>
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</keywords>
<keywords scheme="MESH" qualifier="imagerie diagnostique" xml:lang="fr"><term>Fascia</term>
<term>Hépatomégalie</term>
<term>Lymphadénopathie</term>
<term>Lymphoedème</term>
<term>Maladies auto-immunes</term>
<term>Muscles squelettiques</term>
<term>Polymyosite</term>
<term>Sclérodermie localisée</term>
<term>Splénomégalie</term>
</keywords>
<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr"><term>Centrioles</term>
<term>Hépatomégalie</term>
<term>Lymphadénopathie</term>
<term>Lymphoedème</term>
<term>Maladies auto-immunes</term>
<term>Polymyosite</term>
<term>Sclérodermie localisée</term>
<term>Splénomégalie</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Autoimmune Diseases</term>
<term>Centrioles</term>
<term>Hepatomegaly</term>
<term>Lymphadenopathy</term>
<term>Lymphedema</term>
<term>Polymyositis</term>
<term>Scleroderma, Localized</term>
<term>Splenomegaly</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Autoimmune Diseases</term>
<term>Fascia</term>
<term>Lymph Nodes</term>
<term>Lymphadenopathy</term>
<term>Muscle, Skeletal</term>
<term>Polymyositis</term>
<term>Scleroderma, Localized</term>
<term>Skin</term>
</keywords>
<keywords scheme="MESH" qualifier="sang" xml:lang="fr"><term>Autoanticorps</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Glucocorticoids</term>
<term>Prednisolone</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr"><term>Lymphadénopathie</term>
<term>Maladies auto-immunes</term>
<term>Polymyosite</term>
<term>Sclérodermie localisée</term>
</keywords>
<keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr"><term>Glucocorticoïdes</term>
<term>Prednisolone</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Electromyography</term>
<term>Female</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Middle Aged</term>
<term>Tomography, X-Ray Computed</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adulte d'âge moyen</term>
<term>Femelle</term>
<term>Humains</term>
<term>Imagerie par résonance magnétique</term>
<term>Tomodensitométrie</term>
<term>Électromyographie</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Localized scleroderma is an inflammatory disorder affecting the skin and underlying tissues, a certain subset of which develops other autoimmune diseases on the basis of a prominent autoimmune background. We here report a unique case of linear scleroderma presenting with a sclerotic plaque on the left thigh, multiple lymphadenopathy in bilateral inguinal and para-aortic lymph nodes, and hepatosplenomegaly, who later developed polymyositis. We describe the detailed disease course of our case and discuss the clinical significance of multiple lymphadenopathy in localized scleroderma based on a review of published work.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">27129435</PMID>
<DateCreated><Year>2016</Year>
<Month>04</Month>
<Day>30</Day>
</DateCreated>
<DateCompleted><Year>2017</Year>
<Month>05</Month>
<Day>15</Day>
</DateCompleted>
<DateRevised><Year>2017</Year>
<Month>05</Month>
<Day>15</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1346-8138</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>43</Volume>
<Issue>10</Issue>
<PubDate><Year>2016</Year>
<Month>Oct</Month>
</PubDate>
</JournalIssue>
<Title>The Journal of dermatology</Title>
<ISOAbbreviation>J. Dermatol.</ISOAbbreviation>
</Journal>
<ArticleTitle>Linear scleroderma with prominent multiple lymphadenopathy followed by the development of polymyositis: A case report and review of published work.</ArticleTitle>
<Pagination><MedlinePgn>1224-1227</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/1346-8138.13424</ELocationID>
<Abstract><AbstractText>Localized scleroderma is an inflammatory disorder affecting the skin and underlying tissues, a certain subset of which develops other autoimmune diseases on the basis of a prominent autoimmune background. We here report a unique case of linear scleroderma presenting with a sclerotic plaque on the left thigh, multiple lymphadenopathy in bilateral inguinal and para-aortic lymph nodes, and hepatosplenomegaly, who later developed polymyositis. We describe the detailed disease course of our case and discuss the clinical significance of multiple lymphadenopathy in localized scleroderma based on a review of published work.</AbstractText>
<CopyrightInformation>© 2016 Japanese Dermatological Association.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Takahashi</LastName>
<ForeName>Takehiro</ForeName>
<Initials>T</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Asano</LastName>
<ForeName>Yoshihide</ForeName>
<Initials>Y</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan. yasano-tky@umin.ac.jp.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Hirakawa</LastName>
<ForeName>Maiko</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Nakamura</LastName>
<ForeName>Kouki</ForeName>
<Initials>K</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Saigusa</LastName>
<ForeName>Ryosuke</ForeName>
<Initials>R</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Aozasa</LastName>
<ForeName>Naohiko</ForeName>
<Initials>N</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Sumida</LastName>
<ForeName>Hayakazu</ForeName>
<Initials>H</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Fujita</LastName>
<ForeName>Hideki</ForeName>
<Initials>H</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Sugaya</LastName>
<ForeName>Makoto</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Ohmori</LastName>
<ForeName>Aki</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Shimizu</LastName>
<ForeName>Jun</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Sato</LastName>
<ForeName>Shinichi</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D016454">Review</PublicationType>
</PublicationTypeList>
</Article>
<MedlineJournalInfo><Country>England</Country>
<MedlineTA>J Dermatol</MedlineTA>
<NlmUniqueID>7600545</NlmUniqueID>
<ISSNLinking>0385-2407</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D001323">Autoantibodies</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D005938">Glucocorticoids</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>9PHQ9Y1OLM</RegistryNumber>
<NameOfSubstance UI="D011239">Prednisolone</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D001323" MajorTopicYN="N">Autoantibodies</DescriptorName>
<QualifierName UI="Q000097" MajorTopicYN="N">blood</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D001327" MajorTopicYN="N">Autoimmune Diseases</DescriptorName>
<QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName>
<QualifierName UI="Q000188" MajorTopicYN="N">drug therapy</QualifierName>
<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002502" MajorTopicYN="N">Centrioles</DescriptorName>
<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004576" MajorTopicYN="N">Electromyography</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005205" MajorTopicYN="N">Fascia</DescriptorName>
<QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005938" MajorTopicYN="N">Glucocorticoids</DescriptorName>
<QualifierName UI="Q000627" MajorTopicYN="N">therapeutic use</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006529" MajorTopicYN="N">Hepatomegaly</DescriptorName>
<QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName>
<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008198" MajorTopicYN="N">Lymph Nodes</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000072281" MajorTopicYN="N">Lymphadenopathy</DescriptorName>
<QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName>
<QualifierName UI="Q000188" MajorTopicYN="N">drug therapy</QualifierName>
<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName>
<QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName>
<QualifierName UI="Q000276" MajorTopicYN="Y">immunology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008279" MajorTopicYN="N">Magnetic Resonance Imaging</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D018482" MajorTopicYN="N">Muscle, Skeletal</DescriptorName>
<QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName>
<QualifierName UI="Q000201" MajorTopicYN="N">enzymology</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D017285" MajorTopicYN="N">Polymyositis</DescriptorName>
<QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName>
<QualifierName UI="Q000188" MajorTopicYN="N">drug therapy</QualifierName>
<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D011239" MajorTopicYN="N">Prednisolone</DescriptorName>
<QualifierName UI="Q000627" MajorTopicYN="N">therapeutic use</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012594" MajorTopicYN="N">Scleroderma, Localized</DescriptorName>
<QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName>
<QualifierName UI="Q000188" MajorTopicYN="N">drug therapy</QualifierName>
<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012867" MajorTopicYN="N">Skin</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D013163" MajorTopicYN="N">Splenomegaly</DescriptorName>
<QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName>
<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D014057" MajorTopicYN="N">Tomography, X-Ray Computed</DescriptorName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="Y">hepatosplenomegaly</Keyword>
<Keyword MajorTopicYN="Y">immune abnormality</Keyword>
<Keyword MajorTopicYN="Y">linear scleroderma</Keyword>
<Keyword MajorTopicYN="Y">lymphadenopathy</Keyword>
<Keyword MajorTopicYN="Y">polymyositis</Keyword>
</KeywordList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="received"><Year>2016</Year>
<Month>01</Month>
<Day>28</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted"><Year>2016</Year>
<Month>03</Month>
<Day>14</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed"><Year>2016</Year>
<Month>5</Month>
<Day>1</Day>
<Hour>6</Hour>
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<PubMedPubDate PubStatus="medline"><Year>2017</Year>
<Month>5</Month>
<Day>16</Day>
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<Minute>0</Minute>
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<PubMedPubDate PubStatus="entrez"><Year>2016</Year>
<Month>5</Month>
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<Hour>6</Hour>
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</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">27129435</ArticleId>
<ArticleId IdType="doi">10.1111/1346-8138.13424</ArticleId>
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</PubmedData>
</pubmed>
<affiliations><list><country><li>Japon</li>
</country>
<region><li>Région de Kantō</li>
</region>
<settlement><li>Tokyo</li>
</settlement>
</list>
<tree><country name="Japon"><region name="Région de Kantō"><name sortKey="Takahashi, Takehiro" sort="Takahashi, Takehiro" uniqKey="Takahashi T" first="Takehiro" last="Takahashi">Takehiro Takahashi</name>
</region>
<name sortKey="Aozasa, Naohiko" sort="Aozasa, Naohiko" uniqKey="Aozasa N" first="Naohiko" last="Aozasa">Naohiko Aozasa</name>
<name sortKey="Asano, Yoshihide" sort="Asano, Yoshihide" uniqKey="Asano Y" first="Yoshihide" last="Asano">Yoshihide Asano</name>
<name sortKey="Fujita, Hideki" sort="Fujita, Hideki" uniqKey="Fujita H" first="Hideki" last="Fujita">Hideki Fujita</name>
<name sortKey="Hirakawa, Maiko" sort="Hirakawa, Maiko" uniqKey="Hirakawa M" first="Maiko" last="Hirakawa">Maiko Hirakawa</name>
<name sortKey="Nakamura, Kouki" sort="Nakamura, Kouki" uniqKey="Nakamura K" first="Kouki" last="Nakamura">Kouki Nakamura</name>
<name sortKey="Ohmori, Aki" sort="Ohmori, Aki" uniqKey="Ohmori A" first="Aki" last="Ohmori">Aki Ohmori</name>
<name sortKey="Saigusa, Ryosuke" sort="Saigusa, Ryosuke" uniqKey="Saigusa R" first="Ryosuke" last="Saigusa">Ryosuke Saigusa</name>
<name sortKey="Sato, Shinichi" sort="Sato, Shinichi" uniqKey="Sato S" first="Shinichi" last="Sato">Shinichi Sato</name>
<name sortKey="Shimizu, Jun" sort="Shimizu, Jun" uniqKey="Shimizu J" first="Jun" last="Shimizu">Jun Shimizu</name>
<name sortKey="Sugaya, Makoto" sort="Sugaya, Makoto" uniqKey="Sugaya M" first="Makoto" last="Sugaya">Makoto Sugaya</name>
<name sortKey="Sumida, Hayakazu" sort="Sumida, Hayakazu" uniqKey="Sumida H" first="Hayakazu" last="Sumida">Hayakazu Sumida</name>
</country>
</tree>
</affiliations>
</record>

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Linear scleroderma with prominent multiple lymphadenopathy followed by the development of polymyositis: A case report and review of published work.

Linear scleroderma with prominent multiple lymphadenopathy followed by the development of polymyositis: A case report and review of published work.

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