Takayasu's arteritis is a rare chronic granulomatous vasculitis that primarily affects the aorta and its branches. It is estimated that this disease impacts approximately 2.6 million individuals every year, with a higher prevalence among women in their second or third decade of life. In this case report, we describe the presentation and management of a 22-year-old female patient who initially sought medical attention from a neurologist due to upper and lower back pain. Initially, the patient's symptoms were managed conservatively. However, a few months later, she presented to the medical department with a high-grade fever, syncopal episodes, generalized body aches, and swelling in her right arm. The findings from the computed tomography angiography (CTA) revealed diffuse thickening of the entire thoracic and abdominal aorta's walls, long segment luminal narrowing of the proximal left common carotid artery and left subclavian artery, as well as diffuse thickening of the abdominal aorta's wall. This case highlights the importance of recognizing that Takayasu's arteritis can present in an unusual manner. Early diagnosis and management are crucial steps towards providing appropriate care for patients. Due to the potential involvement of various arterial segments, Takayasu's arteritis can manifest with diverse symptoms and complications. Therefore, clinicians should maintain a high index of suspicion when encountering patients with unexplained symptoms, particularly those involving the aorta and its branches. In conclusion, the presented case emphasizes the need for prompt recognition and intervention in Takayasu's arteritis. By increasing awareness of this rare condition and its atypical presentations, healthcare professionals can ensure timely diagnosis and appropriate management, ultimately improving patient outcomes and quality of life. Further research is warranted to enhance our understanding of this complex disease and optimize its management strategies.
| Published in | Cardiology and Cardiovascular Research (Volume 7, Issue 4) |
| DOI | 10.11648/j.ccr.20230704.15 |
| Page(s) | 93-96 |
| Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
| Copyright |
Copyright © The Author(s), 2023. Published by Science Publishing Group |
Takayasu Arteritis, Autoimmune, Autoimmune in Females, Vascular Disease, Large Vessel, Vasculitis
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APA Style
Ahmad, S., Sajjad Ali Khan, M., Bahadori, P., Khan, A., Ahmad, W., et al. (2023). Pakistani Origin Takayasu Arteritis: A Case Report with a Brief Review from Asymptomatic Presentation Till Diagnosis and Clinical Management. Cardiology and Cardiovascular Research, 7(4), 93-96. https://doi.org/10.11648/j.ccr.20230704.15
ACS Style
Ahmad, S.; Sajjad Ali Khan, M.; Bahadori, P.; Khan, A.; Ahmad, W., et al. Pakistani Origin Takayasu Arteritis: A Case Report with a Brief Review from Asymptomatic Presentation Till Diagnosis and Clinical Management. Cardiol. Cardiovasc. Res. 2023, 7(4), 93-96. doi: 10.11648/j.ccr.20230704.15
AMA Style
Ahmad S, Sajjad Ali Khan M, Bahadori P, Khan A, Ahmad W, et al. Pakistani Origin Takayasu Arteritis: A Case Report with a Brief Review from Asymptomatic Presentation Till Diagnosis and Clinical Management. Cardiol Cardiovasc Res. 2023;7(4):93-96. doi: 10.11648/j.ccr.20230704.15
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author = {Shahzad Ahmad and Muhammad Sajjad Ali Khan and Pardis Bahadori and Aimal Khan and Wiqar Ahmad and Muhammad Ilyas and Komal Qayyum and Muhammad Saeed and Musa Bin Bashir},
title = {Pakistani Origin Takayasu Arteritis: A Case Report with a Brief Review from Asymptomatic Presentation Till Diagnosis and Clinical Management},
journal = {Cardiology and Cardiovascular Research},
volume = {7},
number = {4},
pages = {93-96},
doi = {10.11648/j.ccr.20230704.15},
url = {https://doi.org/10.11648/j.ccr.20230704.15},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ccr.20230704.15},
abstract = {Takayasu's arteritis is a rare chronic granulomatous vasculitis that primarily affects the aorta and its branches. It is estimated that this disease impacts approximately 2.6 million individuals every year, with a higher prevalence among women in their second or third decade of life. In this case report, we describe the presentation and management of a 22-year-old female patient who initially sought medical attention from a neurologist due to upper and lower back pain. Initially, the patient's symptoms were managed conservatively. However, a few months later, she presented to the medical department with a high-grade fever, syncopal episodes, generalized body aches, and swelling in her right arm. The findings from the computed tomography angiography (CTA) revealed diffuse thickening of the entire thoracic and abdominal aorta's walls, long segment luminal narrowing of the proximal left common carotid artery and left subclavian artery, as well as diffuse thickening of the abdominal aorta's wall. This case highlights the importance of recognizing that Takayasu's arteritis can present in an unusual manner. Early diagnosis and management are crucial steps towards providing appropriate care for patients. Due to the potential involvement of various arterial segments, Takayasu's arteritis can manifest with diverse symptoms and complications. Therefore, clinicians should maintain a high index of suspicion when encountering patients with unexplained symptoms, particularly those involving the aorta and its branches. In conclusion, the presented case emphasizes the need for prompt recognition and intervention in Takayasu's arteritis. By increasing awareness of this rare condition and its atypical presentations, healthcare professionals can ensure timely diagnosis and appropriate management, ultimately improving patient outcomes and quality of life. Further research is warranted to enhance our understanding of this complex disease and optimize its management strategies.
},
year = {2023}
}
TY - JOUR T1 - Pakistani Origin Takayasu Arteritis: A Case Report with a Brief Review from Asymptomatic Presentation Till Diagnosis and Clinical Management AU - Shahzad Ahmad AU - Muhammad Sajjad Ali Khan AU - Pardis Bahadori AU - Aimal Khan AU - Wiqar Ahmad AU - Muhammad Ilyas AU - Komal Qayyum AU - Muhammad Saeed AU - Musa Bin Bashir Y1 - 2023/11/29 PY - 2023 N1 - https://doi.org/10.11648/j.ccr.20230704.15 DO - 10.11648/j.ccr.20230704.15 T2 - Cardiology and Cardiovascular Research JF - Cardiology and Cardiovascular Research JO - Cardiology and Cardiovascular Research SP - 93 EP - 96 PB - Science Publishing Group SN - 2578-8914 UR - https://doi.org/10.11648/j.ccr.20230704.15 AB - Takayasu's arteritis is a rare chronic granulomatous vasculitis that primarily affects the aorta and its branches. It is estimated that this disease impacts approximately 2.6 million individuals every year, with a higher prevalence among women in their second or third decade of life. In this case report, we describe the presentation and management of a 22-year-old female patient who initially sought medical attention from a neurologist due to upper and lower back pain. Initially, the patient's symptoms were managed conservatively. However, a few months later, she presented to the medical department with a high-grade fever, syncopal episodes, generalized body aches, and swelling in her right arm. The findings from the computed tomography angiography (CTA) revealed diffuse thickening of the entire thoracic and abdominal aorta's walls, long segment luminal narrowing of the proximal left common carotid artery and left subclavian artery, as well as diffuse thickening of the abdominal aorta's wall. This case highlights the importance of recognizing that Takayasu's arteritis can present in an unusual manner. Early diagnosis and management are crucial steps towards providing appropriate care for patients. Due to the potential involvement of various arterial segments, Takayasu's arteritis can manifest with diverse symptoms and complications. Therefore, clinicians should maintain a high index of suspicion when encountering patients with unexplained symptoms, particularly those involving the aorta and its branches. In conclusion, the presented case emphasizes the need for prompt recognition and intervention in Takayasu's arteritis. By increasing awareness of this rare condition and its atypical presentations, healthcare professionals can ensure timely diagnosis and appropriate management, ultimately improving patient outcomes and quality of life. Further research is warranted to enhance our understanding of this complex disease and optimize its management strategies. VL - 7 IS - 4 ER -
Department of Cardiology, Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China
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