Non-X-linked hyperimmunoglobulin M syndrome with chronic interstitial pneumonitis.
Identifieur interne : 000687 ( PubMed/Checkpoint ); précédent : 000686; suivant : 000688Non-X-linked hyperimmunoglobulin M syndrome with chronic interstitial pneumonitis.
Auteurs : A. Quezada ; X. Norambuena ; R. González ; S M Ramos ; A. Chávez ; S. GonzálezSource :
- Journal of investigational allergology & clinical immunology [ 1018-9068 ]
Descripteurs français
- KwdFr :
- Chromosome X (génétique), Enfant, Femelle, Humains, Hypergammaglobulinémie (), Hypergammaglobulinémie (anatomopathologie), Hypergammaglobulinémie (physiopathologie), Immunoglobuline M (sang), Liaison génétique, Maladie chronique, Pneumopathies interstitielles (), Pneumopathies interstitielles (anatomopathologie), Pneumopathies interstitielles (physiopathologie), Poumon (anatomopathologie), Syndrome.
- MESH :
- anatomopathologie : Hypergammaglobulinémie, Pneumopathies interstitielles, Poumon.
- génétique : Chromosome X.
- physiopathologie : Hypergammaglobulinémie, Pneumopathies interstitielles.
- sang : Immunoglobuline M.
- Enfant, Femelle, Humains, Hypergammaglobulinémie, Liaison génétique, Maladie chronique, Pneumopathies interstitielles, Syndrome.
English descriptors
- KwdEn :
- Child, Chronic Disease, Female, Genetic Linkage, Humans, Hypergammaglobulinemia (complications), Hypergammaglobulinemia (pathology), Hypergammaglobulinemia (physiopathology), Hypergammaglobulinemia (therapy), Immunoglobulin M (blood), Lung (pathology), Lung Diseases, Interstitial (complications), Lung Diseases, Interstitial (pathology), Lung Diseases, Interstitial (physiopathology), Syndrome, X Chromosome (genetics).
- MESH :
- chemical , blood : Immunoglobulin M.
- complications : Hypergammaglobulinemia, Lung Diseases, Interstitial.
- genetics : X Chromosome.
- pathology : Hypergammaglobulinemia, Lung, Lung Diseases, Interstitial.
- physiopathology : Hypergammaglobulinemia, Lung Diseases, Interstitial.
- therapy : Hypergammaglobulinemia.
- Child, Chronic Disease, Female, Genetic Linkage, Humans, Syndrome.
Abstract
Hyperimmunoglobulin M (IgM) syndrome is a rare primary immunodeficiency disorder, and the non-X-linked form of this syndrome is even more infrequent. We report the clinical case of a 6-year-old girl. Her disease began at the age of 1 year when she experienced bronchial obstruction. When she was 3 years old she developed severe recurrent respiratory infections of unusual clinical course. Serum IgM was elevated and the other serum immunoglobulins were absent. Cellular immune response was impaired, with severe depression of delayed hypersensitive cutaneous response and of proliferative response to mitogens. The CD40 ligand expression decreased. Chest CT scan showed areas of lung condensation, bronchial dilatation and signs suggesting interstitial pneumonitis. The latter was confirmed by a biopsy showing a high number of Langerhans' cells and an early-stage fibrosis. She was treated with antibiotics, inhaled bronchodilators and corticosteroids, intravenous immunoglobulin, chloroquine and prednisone. Despite the substitution therapy, her clinical course was slow, with respiratory infections and oxygen dependance. The follow-up thoracoscopic biopsy performed after 18 months of immunosuppressant therapy showed a progression of fibrosis and a decrease in the inflammatory infiltrate.
PubMed: 11206940
Affiliations:
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Chávez</name></author><author><name sortKey="Gonzalez, S" sort="Gonzalez, S" uniqKey="Gonzalez S" first="S" last="González">S. 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Quezada</name><affiliation><nlm:affiliation>Department of Pediatrics, School of Medicine, University of Chile, Santiago.</nlm:affiliation><wicri:noCountry code="subField">Santiago</wicri:noCountry></affiliation></author><author><name sortKey="Norambuena, X" sort="Norambuena, X" uniqKey="Norambuena X" first="X" last="Norambuena">X. Norambuena</name></author><author><name sortKey="Gonzalez, R" sort="Gonzalez, R" uniqKey="Gonzalez R" first="R" last="González">R. González</name></author><author><name sortKey="Ramos, S M" sort="Ramos, S M" uniqKey="Ramos S" first="S M" last="Ramos">S M Ramos</name></author><author><name sortKey="Chavez, A" sort="Chavez, A" uniqKey="Chavez A" first="A" last="Chávez">A. Chávez</name></author><author><name sortKey="Gonzalez, S" sort="Gonzalez, S" uniqKey="Gonzalez S" first="S" last="González">S. 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We report the clinical case of a 6-year-old girl. Her disease began at the age of 1 year when she experienced bronchial obstruction. When she was 3 years old she developed severe recurrent respiratory infections of unusual clinical course. Serum IgM was elevated and the other serum immunoglobulins were absent. Cellular immune response was impaired, with severe depression of delayed hypersensitive cutaneous response and of proliferative response to mitogens. The CD40 ligand expression decreased. Chest CT scan showed areas of lung condensation, bronchial dilatation and signs suggesting interstitial pneumonitis. The latter was confirmed by a biopsy showing a high number of Langerhans' cells and an early-stage fibrosis. She was treated with antibiotics, inhaled bronchodilators and corticosteroids, intravenous immunoglobulin, chloroquine and prednisone. Despite the substitution therapy, her clinical course was slow, with respiratory infections and oxygen dependance. The follow-up thoracoscopic biopsy performed after 18 months of immunosuppressant therapy showed a progression of fibrosis and a decrease in the inflammatory infiltrate.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">11206940</PMID><DateCompleted><Year>2001</Year><Month>06</Month><Day>21</Day></DateCompleted><DateRevised><Year>2013</Year><Month>07</Month><Day>31</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">1018-9068</ISSN><JournalIssue CitedMedium="Print"><Volume>10</Volume><Issue>6</Issue><PubDate><MedlineDate>2000 Nov-Dec</MedlineDate></PubDate></JournalIssue><Title>Journal of investigational allergology & clinical immunology</Title><ISOAbbreviation>J Investig Allergol Clin Immunol</ISOAbbreviation></Journal><ArticleTitle>Non-X-linked hyperimmunoglobulin M syndrome with chronic interstitial pneumonitis.</ArticleTitle><Pagination><MedlinePgn>375-9</MedlinePgn></Pagination><Abstract><AbstractText>Hyperimmunoglobulin M (IgM) syndrome is a rare primary immunodeficiency disorder, and the non-X-linked form of this syndrome is even more infrequent. We report the clinical case of a 6-year-old girl. Her disease began at the age of 1 year when she experienced bronchial obstruction. When she was 3 years old she developed severe recurrent respiratory infections of unusual clinical course. Serum IgM was elevated and the other serum immunoglobulins were absent. Cellular immune response was impaired, with severe depression of delayed hypersensitive cutaneous response and of proliferative response to mitogens. The CD40 ligand expression decreased. Chest CT scan showed areas of lung condensation, bronchial dilatation and signs suggesting interstitial pneumonitis. The latter was confirmed by a biopsy showing a high number of Langerhans' cells and an early-stage fibrosis. She was treated with antibiotics, inhaled bronchodilators and corticosteroids, intravenous immunoglobulin, chloroquine and prednisone. Despite the substitution therapy, her clinical course was slow, with respiratory infections and oxygen dependance. The follow-up thoracoscopic biopsy performed after 18 months of immunosuppressant therapy showed a progression of fibrosis and a decrease in the inflammatory infiltrate.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Quezada</LastName><ForeName>A</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Department of Pediatrics, School of Medicine, University of Chile, Santiago.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Norambuena</LastName><ForeName>X</ForeName><Initials>X</Initials></Author><Author ValidYN="Y"><LastName>González</LastName><ForeName>R</ForeName><Initials>R</Initials></Author><Author ValidYN="Y"><LastName>Ramos</LastName><ForeName>S M</ForeName><Initials>SM</Initials></Author><Author ValidYN="Y"><LastName>Chávez</LastName><ForeName>A</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>González</LastName><ForeName>S</ForeName><Initials>S</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>Spain</Country><MedlineTA>J Investig Allergol Clin Immunol</MedlineTA><NlmUniqueID>9107858</NlmUniqueID><ISSNLinking>1018-9068</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D007075">Immunoglobulin M</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002908" MajorTopicYN="N">Chronic Disease</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008040" MajorTopicYN="N">Genetic Linkage</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006942" MajorTopicYN="N">Hypergammaglobulinemia</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName><QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007075" MajorTopicYN="Y">Immunoglobulin M</DescriptorName><QualifierName UI="Q000097" MajorTopicYN="Y">blood</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008168" MajorTopicYN="N">Lung</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017563" MajorTopicYN="N">Lung Diseases, Interstitial</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013577" MajorTopicYN="N">Syndrome</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014960" MajorTopicYN="N">X Chromosome</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2001</Year><Month>2</Month><Day>24</Day><Hour>12</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2001</Year><Month>6</Month><Day>22</Day><Hour>10</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2001</Year><Month>2</Month><Day>24</Day><Hour>12</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">11206940</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list></list><tree><noCountry><name sortKey="Chavez, A" sort="Chavez, A" uniqKey="Chavez A" first="A" last="Chávez">A. Chávez</name><name sortKey="Gonzalez, R" sort="Gonzalez, R" uniqKey="Gonzalez R" first="R" last="González">R. González</name><name sortKey="Gonzalez, S" sort="Gonzalez, S" uniqKey="Gonzalez S" first="S" last="González">S. González</name><name sortKey="Norambuena, X" sort="Norambuena, X" uniqKey="Norambuena X" first="X" last="Norambuena">X. Norambuena</name><name sortKey="Quezada, A" sort="Quezada, A" uniqKey="Quezada A" first="A" last="Quezada">A. Quezada</name><name sortKey="Ramos, S M" sort="Ramos, S M" uniqKey="Ramos S" first="S M" last="Ramos">S M Ramos</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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