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Large vessel vasculitis
Takayasu arteritis is a chronic granulomatous disease of the aorta and its major branches that usually affects women during the second and third decades of life, but it has been reported in young children. This review details the clinical, pathological and radiological features, differential diagnos...
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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2855435/ https://www.ncbi.nlm.nih.gov/pubmed/19844748 http://dx.doi.org/10.1007/s00467-009-1312-9 |
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author | Gulati, Ashima Bagga, Arvind |
author_facet | Gulati, Ashima Bagga, Arvind |
author_sort | Gulati, Ashima |
collection | PubMed |
description | Takayasu arteritis is a chronic granulomatous disease of the aorta and its major branches that usually affects women during the second and third decades of life, but it has been reported in young children. This review details the clinical, pathological and radiological features, differential diagnoses and management of the condition, focusing chiefly on the disease in children. The recent definition of Takayasu arteritis is discussed. The condition should be considered in patients with unexplained arterial hypertension or unexplained inflammatory syndromes without signs of localization. Since the disease may be life-threatening and progressive, early recognition is necessary to initiate appropriate therapy. Patients with persistent ischaemic symptoms including hypertension might benefit from revascularization procedures. |
format | Text |
id | pubmed-2855435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-28554352010-04-21 Large vessel vasculitis Gulati, Ashima Bagga, Arvind Pediatr Nephrol Educational Review Takayasu arteritis is a chronic granulomatous disease of the aorta and its major branches that usually affects women during the second and third decades of life, but it has been reported in young children. This review details the clinical, pathological and radiological features, differential diagnoses and management of the condition, focusing chiefly on the disease in children. The recent definition of Takayasu arteritis is discussed. The condition should be considered in patients with unexplained arterial hypertension or unexplained inflammatory syndromes without signs of localization. Since the disease may be life-threatening and progressive, early recognition is necessary to initiate appropriate therapy. Patients with persistent ischaemic symptoms including hypertension might benefit from revascularization procedures. Springer-Verlag 2009-10-17 2010-06 /pmc/articles/PMC2855435/ /pubmed/19844748 http://dx.doi.org/10.1007/s00467-009-1312-9 Text en © IPNA 2009 |
spellingShingle | Educational Review Gulati, Ashima Bagga, Arvind Large vessel vasculitis |
title | Large vessel vasculitis |
title_full | Large vessel vasculitis |
title_fullStr | Large vessel vasculitis |
title_full_unstemmed | Large vessel vasculitis |
title_short | Large vessel vasculitis |
title_sort | large vessel vasculitis |
topic | Educational Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2855435/ https://www.ncbi.nlm.nih.gov/pubmed/19844748 http://dx.doi.org/10.1007/s00467-009-1312-9 |
work_keys_str_mv | AT gulatiashima largevesselvasculitis AT baggaarvind largevesselvasculitis |