A stab in the dark: a case report of an atypical presentation of giant cell arteritis (GCA)
A stab in the dark: a case report of an atypical presentation of giant cell arteritis (GCA)
Background: giant cell arteritis/temporal arteritis (GCA) is an inflammatory condition that affects large to medium vessels such as the aorta and its primary branches. Patients classically present with fatigue, fever, headache, jaw claudication and in severe cases, may suffer either transient (amaurosis fugax) or permanent visual loss. The reference standard for diagnosis is the temporal artery biopsy (TAB) and the mainstay of treatment is with immunosuppression. Our patient JG, presented with a range of non-specific symptoms that mimicked generalised sepsis, but was ultimately diagnosed with GCA through effective, methodical multi-disciplinary team (MDT) work.
Clinical case: JG, an 81 year old gentleman, presented acutely with a 3–4 weeks history of fatigue, lethargy, pyrexia and a marked inflammatory response suggestive of a sepsis but without a clear primary source or clinical features of vasculitis. His inflammatory markers were markedly raised although his erythrocyte sedimentation rate (ESR) was not elevated. He was initially treated for sepsis of unknown origin however, body imaging after admission suggested a possible infection around a previous aortic graft site. This was refuted in subsequent 18F-fluorodeoxyglucose-positron emission tomography (FDG-PET/CT) scanning. Microbiological, parasitic, as well as autoimmune assays were unremarkable. He underwent a TAB which was diagnostic for GCA and as a result, was started on oral corticosteroids with immediate symptom relief. He was discharged and followed up on an outpatient basis.
Conclusions: this case highlights how a vasculitis can present with a range of non-specific symptoms that may resemble a fever of unknown origin (FUO)/sepsis that can lead to a delay in making the correct diagnosis. It also highlights the importance of considering a diagnosis of vasculitis in patients who present with a FUO where there is no clear focus of infection. Delays in diagnosis and management of these conditions can potentially lead to significant irreversible morbidity.
McCausland, Beth
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Desai, David
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Harvard, David
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Kaur, Yasmin
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Yener, Asalet
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Bradley, Emma
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Patel, Harnish
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McCausland, Beth
761ba09b-a55b-4752-9e0c-73a311ee26f6
Desai, David
7f2eb189-3fb2-4d96-9d5a-14656c26f607
Harvard, David
52617a31-3a35-4b32-8931-a91dbd424d9e
Kaur, Yasmin
f1eb8349-59a5-4069-a2ea-812bbb2b418e
Yener, Asalet
ea1f7c51-e1b5-45d0-8f83-ba3c7fcab198
Bradley, Emma
d9ef98a3-a7e8-4a9a-87b9-f38452a9f50b
Patel, Harnish
e1c0826f-d14e-49f3-8049-5b945d185523
McCausland, Beth, Desai, David, Harvard, David, Kaur, Yasmin, Yener, Asalet, Bradley, Emma and Patel, Harnish
(2018)
A stab in the dark: a case report of an atypical presentation of giant cell arteritis (GCA).
Geriatrics, 3 (3).
(doi:10.3390/geriatrics3030036).
Abstract
Background: giant cell arteritis/temporal arteritis (GCA) is an inflammatory condition that affects large to medium vessels such as the aorta and its primary branches. Patients classically present with fatigue, fever, headache, jaw claudication and in severe cases, may suffer either transient (amaurosis fugax) or permanent visual loss. The reference standard for diagnosis is the temporal artery biopsy (TAB) and the mainstay of treatment is with immunosuppression. Our patient JG, presented with a range of non-specific symptoms that mimicked generalised sepsis, but was ultimately diagnosed with GCA through effective, methodical multi-disciplinary team (MDT) work.
Clinical case: JG, an 81 year old gentleman, presented acutely with a 3–4 weeks history of fatigue, lethargy, pyrexia and a marked inflammatory response suggestive of a sepsis but without a clear primary source or clinical features of vasculitis. His inflammatory markers were markedly raised although his erythrocyte sedimentation rate (ESR) was not elevated. He was initially treated for sepsis of unknown origin however, body imaging after admission suggested a possible infection around a previous aortic graft site. This was refuted in subsequent 18F-fluorodeoxyglucose-positron emission tomography (FDG-PET/CT) scanning. Microbiological, parasitic, as well as autoimmune assays were unremarkable. He underwent a TAB which was diagnostic for GCA and as a result, was started on oral corticosteroids with immediate symptom relief. He was discharged and followed up on an outpatient basis.
Conclusions: this case highlights how a vasculitis can present with a range of non-specific symptoms that may resemble a fever of unknown origin (FUO)/sepsis that can lead to a delay in making the correct diagnosis. It also highlights the importance of considering a diagnosis of vasculitis in patients who present with a FUO where there is no clear focus of infection. Delays in diagnosis and management of these conditions can potentially lead to significant irreversible morbidity.
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Accepted/In Press date: 27 June 2018
e-pub ahead of print date: 29 June 2018
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Local EPrints ID: 422091
URI: http://eprints.soton.ac.uk/id/eprint/422091
PURE UUID: aa5ad1be-7947-4308-b4a6-84e32a37c573
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Date deposited: 16 Jul 2018 16:30
Last modified: 16 Mar 2024 03:53
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Author:
Beth McCausland
Author:
David Desai
Author:
David Harvard
Author:
Yasmin Kaur
Author:
Asalet Yener
Author:
Emma Bradley
Author:
Harnish Patel
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