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Chronic periaortitis (retroperitoneal fibrosis) concurrent with giant cell arteritis: a case report
INTRODUCTION: Giant cell arteritis is the most common form of large-vessel vasculitides. However, it is probable that extracranial involvement is underdiagnosed in patients with classical giant cell arteritis. In the recent literature most cases of giant cell arteritis have been described in conjunc...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4070639/ https://www.ncbi.nlm.nih.gov/pubmed/24885445 http://dx.doi.org/10.1186/1752-1947-8-167 |
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author | Protopsaltis, Ioannis Sotiropoulos, Athanasios Foteinos, Argyrios Manoloudaki, Kassiani Boki, Kiriaki Linardaki, Garifallia Papazafiropoulou, Athanasia Antonopoulos, Stavros |
author_facet | Protopsaltis, Ioannis Sotiropoulos, Athanasios Foteinos, Argyrios Manoloudaki, Kassiani Boki, Kiriaki Linardaki, Garifallia Papazafiropoulou, Athanasia Antonopoulos, Stavros |
author_sort | Protopsaltis, Ioannis |
collection | PubMed |
description | INTRODUCTION: Giant cell arteritis is the most common form of large-vessel vasculitides. However, it is probable that extracranial involvement is underdiagnosed in patients with classical giant cell arteritis. In the recent literature most cases of giant cell arteritis have been described in conjunction with aortic aneurysms or dissections. Nonetheless the coexistence of giant cell arteritis and retroperitoneal fibrosis is extremely rare. Here, we describe a case of giant cell arteritis at a very early clinical stage, in a woman with coexistence of retroperitoneal fibrosis. CASE PRESENTATION: We report a case of giant cell arteritis at a very early clinical stage, in a 47-year-old Greek woman with coexistence of retroperitoneal fibrosis who was admitted to our hospital with a history of high-grade fever and mild right periumbilical abdominal pain for the past 30 days. In the context of fever of unknown origin, an abdomen computed tomography was ordered. A temporal artery biopsy was also performed because during hospitalization she complained of a headache. Examination of eosin and hematoxylin slides from biopsy specimens of her temporal artery, showed lesions consisting of predominantly lymphocytes, few plasma cells and occasional polymorphonuclear leucocytes. In addition no giant cells were detected in examining biopsies at multiple levels. This was consistent with giant cell arteritis according to the American college of Rheumatology criteria. An abdomen computed tomography revealed the presence of a retroperitoneal soft-tissue mass located anteriorly to the upper infrarenal aorta at the site of the scintigraphic uptake. The computed tomography and magnetic resonance imaging characteristics of the mass were consistent with retroperitoneal fibrosis, and its morphology suggestive of benignity. Our patient started oral prednisolone and was afebrile from day one. CONCLUSIONS: In our experience this is the first case of retroperitoneal fibrosis due to giant cell arteritis occurring at the same time. Involvement of the aorta (aortitis) and its branches has been also observed in a subset of patients with giant cell arteritis. In addition, giant cell arteritis has been associated with a markedly increased risk of aortic aneurysm particularly thoracic aortic aneurysm. |
format | Online Article Text |
id | pubmed-4070639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40706392014-06-26 Chronic periaortitis (retroperitoneal fibrosis) concurrent with giant cell arteritis: a case report Protopsaltis, Ioannis Sotiropoulos, Athanasios Foteinos, Argyrios Manoloudaki, Kassiani Boki, Kiriaki Linardaki, Garifallia Papazafiropoulou, Athanasia Antonopoulos, Stavros J Med Case Rep Case Report INTRODUCTION: Giant cell arteritis is the most common form of large-vessel vasculitides. However, it is probable that extracranial involvement is underdiagnosed in patients with classical giant cell arteritis. In the recent literature most cases of giant cell arteritis have been described in conjunction with aortic aneurysms or dissections. Nonetheless the coexistence of giant cell arteritis and retroperitoneal fibrosis is extremely rare. Here, we describe a case of giant cell arteritis at a very early clinical stage, in a woman with coexistence of retroperitoneal fibrosis. CASE PRESENTATION: We report a case of giant cell arteritis at a very early clinical stage, in a 47-year-old Greek woman with coexistence of retroperitoneal fibrosis who was admitted to our hospital with a history of high-grade fever and mild right periumbilical abdominal pain for the past 30 days. In the context of fever of unknown origin, an abdomen computed tomography was ordered. A temporal artery biopsy was also performed because during hospitalization she complained of a headache. Examination of eosin and hematoxylin slides from biopsy specimens of her temporal artery, showed lesions consisting of predominantly lymphocytes, few plasma cells and occasional polymorphonuclear leucocytes. In addition no giant cells were detected in examining biopsies at multiple levels. This was consistent with giant cell arteritis according to the American college of Rheumatology criteria. An abdomen computed tomography revealed the presence of a retroperitoneal soft-tissue mass located anteriorly to the upper infrarenal aorta at the site of the scintigraphic uptake. The computed tomography and magnetic resonance imaging characteristics of the mass were consistent with retroperitoneal fibrosis, and its morphology suggestive of benignity. Our patient started oral prednisolone and was afebrile from day one. CONCLUSIONS: In our experience this is the first case of retroperitoneal fibrosis due to giant cell arteritis occurring at the same time. Involvement of the aorta (aortitis) and its branches has been also observed in a subset of patients with giant cell arteritis. In addition, giant cell arteritis has been associated with a markedly increased risk of aortic aneurysm particularly thoracic aortic aneurysm. BioMed Central 2014-05-27 /pmc/articles/PMC4070639/ /pubmed/24885445 http://dx.doi.org/10.1186/1752-1947-8-167 Text en Copyright © 2014 Protopsaltis et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Protopsaltis, Ioannis Sotiropoulos, Athanasios Foteinos, Argyrios Manoloudaki, Kassiani Boki, Kiriaki Linardaki, Garifallia Papazafiropoulou, Athanasia Antonopoulos, Stavros Chronic periaortitis (retroperitoneal fibrosis) concurrent with giant cell arteritis: a case report |
title | Chronic periaortitis (retroperitoneal fibrosis) concurrent with giant cell arteritis: a case report |
title_full | Chronic periaortitis (retroperitoneal fibrosis) concurrent with giant cell arteritis: a case report |
title_fullStr | Chronic periaortitis (retroperitoneal fibrosis) concurrent with giant cell arteritis: a case report |
title_full_unstemmed | Chronic periaortitis (retroperitoneal fibrosis) concurrent with giant cell arteritis: a case report |
title_short | Chronic periaortitis (retroperitoneal fibrosis) concurrent with giant cell arteritis: a case report |
title_sort | chronic periaortitis (retroperitoneal fibrosis) concurrent with giant cell arteritis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4070639/ https://www.ncbi.nlm.nih.gov/pubmed/24885445 http://dx.doi.org/10.1186/1752-1947-8-167 |
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