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Large vessel vasculitis with rare presentation of acute rhabdomyolysis: A case report and review of literature
BACKGROUND: Musculoskeletal involvement in primary large vessel vasculitis (LVV), including giant cell arteritis and Takayasu's arteritis (TAK), tends to be subacute. With the progression of arterial disease, patients may develop polyarthralgia and myalgias, mainly involving muscle stiffness, l...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131208/ https://www.ncbi.nlm.nih.gov/pubmed/35665112 http://dx.doi.org/10.12998/wjcc.v10.i13.4137 |
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author | Fu, Lan-Jun Hu, Shou-Ci Zhang, Wen Ye, Li-Qing Chen, Hong-Bo Xiang, Xiao-Jun |
author_facet | Fu, Lan-Jun Hu, Shou-Ci Zhang, Wen Ye, Li-Qing Chen, Hong-Bo Xiang, Xiao-Jun |
author_sort | Fu, Lan-Jun |
collection | PubMed |
description | BACKGROUND: Musculoskeletal involvement in primary large vessel vasculitis (LVV), including giant cell arteritis and Takayasu's arteritis (TAK), tends to be subacute. With the progression of arterial disease, patients may develop polyarthralgia and myalgias, mainly involving muscle stiffness, limb/jaw claudication, cold/swelling extremities, etc. Acute development of rhabdomyolysis in addition to aortic aneurysm is uncommon in LVV. Herein, we report a rare case of LVV with the first presentation of acute rhabdomyolysis. CASE SUMMARY: A 70-year-old Asian woman suffering from long-term low back pain was hospitalized due to limb claudication, dark urine and an elevated creatine kinase (CK) level. After treatment with fluid resuscitation and antibiotics, the patient remained febrile. Her workup showed persistent elevated levels of inflammatory markers, and imaging studies revealed an aortic aneurysm. A decreasing CK was evidently combined with elevated inflammatory markers and negativity for anti-neutrophilic cytoplasmic antibodies. LVV was suspected and confirmed by magnetic resonance angiography and positron emission tomography with 18F-fluorodeoxyglucose/computed tomography. With a favourable response to immunosuppressive treatment, her symptoms resolved, and clinical remission was achieved one month later. However, after failing to follow the tapering schedule, the patient was readministered 25 mg/d prednisolone due to disease relapse. Follow-up examinations showed decreased inflammatory markers and substantial improvement in artery lesions after 6 mo of treatment. At the twelve-month follow-up, she was clinically stable and maintained on corticosteroid therapy. CONCLUSION: An exceptional presentation of LVV with acute rhabdomyolysis is described in this case, which exhibited a good response to immunosuppressive therapy, suggesting consideration for a differential diagnosis when evaluating febrile patients with myalgia and elevated CK. Timely use of high-dose steroids until a diagnosis is established may yield a favourable outcome. |
format | Online Article Text |
id | pubmed-9131208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-91312082022-06-04 Large vessel vasculitis with rare presentation of acute rhabdomyolysis: A case report and review of literature Fu, Lan-Jun Hu, Shou-Ci Zhang, Wen Ye, Li-Qing Chen, Hong-Bo Xiang, Xiao-Jun World J Clin Cases Case Report BACKGROUND: Musculoskeletal involvement in primary large vessel vasculitis (LVV), including giant cell arteritis and Takayasu's arteritis (TAK), tends to be subacute. With the progression of arterial disease, patients may develop polyarthralgia and myalgias, mainly involving muscle stiffness, limb/jaw claudication, cold/swelling extremities, etc. Acute development of rhabdomyolysis in addition to aortic aneurysm is uncommon in LVV. Herein, we report a rare case of LVV with the first presentation of acute rhabdomyolysis. CASE SUMMARY: A 70-year-old Asian woman suffering from long-term low back pain was hospitalized due to limb claudication, dark urine and an elevated creatine kinase (CK) level. After treatment with fluid resuscitation and antibiotics, the patient remained febrile. Her workup showed persistent elevated levels of inflammatory markers, and imaging studies revealed an aortic aneurysm. A decreasing CK was evidently combined with elevated inflammatory markers and negativity for anti-neutrophilic cytoplasmic antibodies. LVV was suspected and confirmed by magnetic resonance angiography and positron emission tomography with 18F-fluorodeoxyglucose/computed tomography. With a favourable response to immunosuppressive treatment, her symptoms resolved, and clinical remission was achieved one month later. However, after failing to follow the tapering schedule, the patient was readministered 25 mg/d prednisolone due to disease relapse. Follow-up examinations showed decreased inflammatory markers and substantial improvement in artery lesions after 6 mo of treatment. At the twelve-month follow-up, she was clinically stable and maintained on corticosteroid therapy. CONCLUSION: An exceptional presentation of LVV with acute rhabdomyolysis is described in this case, which exhibited a good response to immunosuppressive therapy, suggesting consideration for a differential diagnosis when evaluating febrile patients with myalgia and elevated CK. Timely use of high-dose steroids until a diagnosis is established may yield a favourable outcome. Baishideng Publishing Group Inc 2022-05-06 2022-05-06 /pmc/articles/PMC9131208/ /pubmed/35665112 http://dx.doi.org/10.12998/wjcc.v10.i13.4137 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Fu, Lan-Jun Hu, Shou-Ci Zhang, Wen Ye, Li-Qing Chen, Hong-Bo Xiang, Xiao-Jun Large vessel vasculitis with rare presentation of acute rhabdomyolysis: A case report and review of literature |
title | Large vessel vasculitis with rare presentation of acute rhabdomyolysis: A case report and review of literature |
title_full | Large vessel vasculitis with rare presentation of acute rhabdomyolysis: A case report and review of literature |
title_fullStr | Large vessel vasculitis with rare presentation of acute rhabdomyolysis: A case report and review of literature |
title_full_unstemmed | Large vessel vasculitis with rare presentation of acute rhabdomyolysis: A case report and review of literature |
title_short | Large vessel vasculitis with rare presentation of acute rhabdomyolysis: A case report and review of literature |
title_sort | large vessel vasculitis with rare presentation of acute rhabdomyolysis: a case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131208/ https://www.ncbi.nlm.nih.gov/pubmed/35665112 http://dx.doi.org/10.12998/wjcc.v10.i13.4137 |
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