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Rare Ischemic Complications of Giant Cell Arteritis: Case Series and Literature Review
Case series Patients: Female, 75-year-old • Female, 76-year-old • Female, 72-year-old Final Diagnosis: Giant cell arteritis Symptoms: Ischemic complications of giant cell arteritis Medication: — Clinical Procedure: — Specialty: General and Internal Medicine • Rheumatology OBJECTIVE: Challenging diff...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578098/ https://www.ncbi.nlm.nih.gov/pubmed/36240129 http://dx.doi.org/10.12659/AJCR.937565 |
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author | Jalaledin, Darya S. Ross, Carolyn Makhzoum, Jean-Paul |
author_facet | Jalaledin, Darya S. Ross, Carolyn Makhzoum, Jean-Paul |
author_sort | Jalaledin, Darya S. |
collection | PubMed |
description | Case series Patients: Female, 75-year-old • Female, 76-year-old • Female, 72-year-old Final Diagnosis: Giant cell arteritis Symptoms: Ischemic complications of giant cell arteritis Medication: — Clinical Procedure: — Specialty: General and Internal Medicine • Rheumatology OBJECTIVE: Challenging differential diagnosis BACKGROUND: Some ischemic complications due to giant cell arteritis (GCA) are rare and underdiagnosed. We describe the clinical features and outcomes of patients with GCA presenting with rare ischemic complications. CASE REPORTS: Our single-center retrospective database of patients with GCA was reviewed from 1994 to 2020. We describe 3 cases of rare ischemic complications secondary to GCA. We review the literature regarding ischemic complications due to GCA and their outcomes. All 3 cases met the American College of Rheumatology criteria for GCA. All patients experienced rare ischemic complications due to GCA. In case 1, the patient presented with a sixth cranial nerve palsy. In case 2, the patient presented with tongue and scalp necrosis, and with permanent visual loss due to anterior ischemic optic neuropathy. In case 3, the patient presented with scalp necrosis. In all 3 cases, the patients received glucocorticoids either intravenously and/or orally, which led to improvement. They all improved within the course of their followup visits. A literature review was performed to identify similar cases and outcomes. CONCLUSIONS: Ischemic complications due to GCA can be part of the initial presentation of the vasculitis, making confirmation of the diagnosis more difficult. Physicians should be aware of these rare complications since rapid diagnosis and initiation of glucocorticoids may alter the course of the disease. |
format | Online Article Text |
id | pubmed-9578098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95780982022-10-31 Rare Ischemic Complications of Giant Cell Arteritis: Case Series and Literature Review Jalaledin, Darya S. Ross, Carolyn Makhzoum, Jean-Paul Am J Case Rep Articles Case series Patients: Female, 75-year-old • Female, 76-year-old • Female, 72-year-old Final Diagnosis: Giant cell arteritis Symptoms: Ischemic complications of giant cell arteritis Medication: — Clinical Procedure: — Specialty: General and Internal Medicine • Rheumatology OBJECTIVE: Challenging differential diagnosis BACKGROUND: Some ischemic complications due to giant cell arteritis (GCA) are rare and underdiagnosed. We describe the clinical features and outcomes of patients with GCA presenting with rare ischemic complications. CASE REPORTS: Our single-center retrospective database of patients with GCA was reviewed from 1994 to 2020. We describe 3 cases of rare ischemic complications secondary to GCA. We review the literature regarding ischemic complications due to GCA and their outcomes. All 3 cases met the American College of Rheumatology criteria for GCA. All patients experienced rare ischemic complications due to GCA. In case 1, the patient presented with a sixth cranial nerve palsy. In case 2, the patient presented with tongue and scalp necrosis, and with permanent visual loss due to anterior ischemic optic neuropathy. In case 3, the patient presented with scalp necrosis. In all 3 cases, the patients received glucocorticoids either intravenously and/or orally, which led to improvement. They all improved within the course of their followup visits. A literature review was performed to identify similar cases and outcomes. CONCLUSIONS: Ischemic complications due to GCA can be part of the initial presentation of the vasculitis, making confirmation of the diagnosis more difficult. Physicians should be aware of these rare complications since rapid diagnosis and initiation of glucocorticoids may alter the course of the disease. International Scientific Literature, Inc. 2022-10-14 /pmc/articles/PMC9578098/ /pubmed/36240129 http://dx.doi.org/10.12659/AJCR.937565 Text en © Am J Case Rep, 2022 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Articles Jalaledin, Darya S. Ross, Carolyn Makhzoum, Jean-Paul Rare Ischemic Complications of Giant Cell Arteritis: Case Series and Literature Review |
title | Rare Ischemic Complications of Giant Cell Arteritis: Case Series and Literature Review |
title_full | Rare Ischemic Complications of Giant Cell Arteritis: Case Series and Literature Review |
title_fullStr | Rare Ischemic Complications of Giant Cell Arteritis: Case Series and Literature Review |
title_full_unstemmed | Rare Ischemic Complications of Giant Cell Arteritis: Case Series and Literature Review |
title_short | Rare Ischemic Complications of Giant Cell Arteritis: Case Series and Literature Review |
title_sort | rare ischemic complications of giant cell arteritis: case series and literature review |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578098/ https://www.ncbi.nlm.nih.gov/pubmed/36240129 http://dx.doi.org/10.12659/AJCR.937565 |
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