Takayasu arteritis: a review
Takayasu arteritis is a well known yet rare form of large vessel vasculitis. This review details the history, clinical features, differential diagnoses, classification, and immunology of the disorder. Suppression of inflammation and preservation of vascular competence are the aims of treatment. As w...
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Published in: | Journal of clinical pathology Vol. 55; no. 7; pp. 481 - 486 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
London
BMJ Publishing Group Ltd and Association of Clinical Pathologists
01-07-2002
BMJ BMJ Publishing Group Ltd BMJ Publishing Group LTD Copyright 2002 Journal of Clinical Pathology |
Subjects: | |
Online Access: | Get full text |
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Summary: | Takayasu arteritis is a well known yet rare form of large vessel vasculitis. This review details the history, clinical features, differential diagnoses, classification, and immunology of the disorder. Suppression of inflammation and preservation of vascular competence are the aims of treatment. As with any rare disease, randomised controlled treatment trials are either lacking or based on small patient numbers, making management decisions difficult. Current evidence based treatments are presented and discussed. |
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Bibliography: | href:jclinpath-55-481.pdf ark:/67375/NVC-73D4M8D2-V istex:3BB69FC9018EB729757419B8EFA7E792603E8273 local:0550481 Correspondence to: Dr S L Johnston, Department of Immunology and Immunogenetics, Southmead Hospital, Westbury on Trym, Bristol BS10 5NB, UK; sljoh@hotmail.com PMID:12101189 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 Correspondence to: Dr S L Johnston, Department of Immunology and Immunogenetics, Southmead Hospital, Westbury on Trym, Bristol BS10 5NB, UK; sljoh@hotmail.com |
ISSN: | 0021-9746 1472-4146 |
DOI: | 10.1136/jcp.55.7.481 |