Erosive rheumatoid arthritis co-existing with systemic lupus erythematosus. A report of a case, also showing atlanto-axial subluxation
Identifieur interne : 003736 ( Main/Exploration ); précédent : 003735; suivant : 003737Erosive rheumatoid arthritis co-existing with systemic lupus erythematosus. A report of a case, also showing atlanto-axial subluxation
Auteurs : D. A. Isenberg [Royaume-Uni] ; A. Tookman [Royaume-Uni] ; A. G. White [Royaume-Uni] ; B. I. Hoffbrand [Royaume-Uni] ; J. Mowbray [Royaume-Uni]Source :
- Clinical Rheumatology [ 0770-3198 ] ; 1982-09-01.
English descriptors
- KwdEn :
- Teeft :
- Arthritis, Azathioprine, Erosive, Erythematosus, Genetic marker, Glomerular capillary basement membranes, Gold therapy, Immune complexes, Lupus, Platelet, Platelet count, Prednisolone, Renal, Renal biopsy, Renal disease, Rheum, Rheumatoid, Rheumatoid arthritis, Same patient, Stiffness, Subluxation, Systemic, Systemic lupus erythematosus, Whittington hospital.
Abstract
Summary: A 28-year old female is described with a 12-year history of seropositive, erosive rheumatoid arthritis. Subsequently, she developed systemic lupus erythematosus diagnosed both serologically and on renal biopsy. As has previously been emphasised, these two diseases occur rarely in the same patient. HLA typing revealed the patient was HLA — B8 positive and that she had inherited this genetic marker from her mother who is Irish, rather than from her West Indian father. The patient has developed marked atlanto-axial subluxation, a feature not noted in six patients previously described as having both diseases.
Url:
DOI: 10.1007/BF02042778
Affiliations:
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Mowbray</name><affiliation wicri:level="2"><country>Royaume-Uni</country><placeName><region type="country">Angleterre</region></placeName><wicri:cityArea>Department of Experimental Pathology, St Mary's Hospital, London</wicri:cityArea></affiliation></author></analytic><monogr></monogr><series><title level="j">Clinical Rheumatology</title><title level="j" type="abbrev">Clin Rheumatol</title><idno type="ISSN">0770-3198</idno><idno type="eISSN">1434-9949</idno><imprint><publisher>Springer-Verlag</publisher><pubPlace>London</pubPlace><date type="published" when="1982-09-01">1982-09-01</date><biblScope unit="volume">1</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="216">216</biblScope><biblScope unit="page" to="220">220</biblScope></imprint><idno type="ISSN">0770-3198</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0770-3198</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Atlanto-axial subluxation</term><term>Rheumatoid Arthritis</term><term>SLE</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Arthritis</term><term>Azathioprine</term><term>Erosive</term><term>Erythematosus</term><term>Genetic marker</term><term>Glomerular capillary basement membranes</term><term>Gold therapy</term><term>Immune complexes</term><term>Lupus</term><term>Platelet</term><term>Platelet count</term><term>Prednisolone</term><term>Renal</term><term>Renal biopsy</term><term>Renal disease</term><term>Rheum</term><term>Rheumatoid</term><term>Rheumatoid arthritis</term><term>Same patient</term><term>Stiffness</term><term>Subluxation</term><term>Systemic</term><term>Systemic lupus erythematosus</term><term>Whittington hospital</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Summary: A 28-year old female is described with a 12-year history of seropositive, erosive rheumatoid arthritis. Subsequently, she developed systemic lupus erythematosus diagnosed both serologically and on renal biopsy. As has previously been emphasised, these two diseases occur rarely in the same patient. HLA typing revealed the patient was HLA — B8 positive and that she had inherited this genetic marker from her mother who is Irish, rather than from her West Indian father. The patient has developed marked atlanto-axial subluxation, a feature not noted in six patients previously described as having both diseases.</div></front></TEI><affiliations><list><country><li>Royaume-Uni</li></country><region><li>Angleterre</li><li>Grand Londres</li></region><settlement><li>Londres</li></settlement></list><tree><country name="Royaume-Uni"><region name="Angleterre"><name sortKey="Isenberg, D A" sort="Isenberg, D A" uniqKey="Isenberg D" first="D. A." last="Isenberg">D. A. Isenberg</name></region><name sortKey="Hoffbrand, B I" sort="Hoffbrand, B I" uniqKey="Hoffbrand B" first="B. I." last="Hoffbrand">B. I. Hoffbrand</name><name sortKey="Mowbray, J" sort="Mowbray, J" uniqKey="Mowbray J" first="J." last="Mowbray">J. Mowbray</name><name sortKey="Tookman, A" sort="Tookman, A" uniqKey="Tookman A" first="A." last="Tookman">A. Tookman</name><name sortKey="White, A G" sort="White, A G" uniqKey="White A" first="A. G." last="White">A. G. White</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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