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Journal articles on the topic 'Takayasu’s arteritis'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Dasgupta, Malay Kumar, Sabyasachi Das, and Debasree Guha. "Steroid Resistant Takayasu Arteritis." Journal of Nepal Paediatric Society 33, no. 2 (2013): 144–46. http://dx.doi.org/10.3126/jnps.v33i2.7113.

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Takayasu’s arteritis (TA), a chronic inflammatory disease affecting the aorta, its branches and the pulmonary arteries has become increasingly recognized as a worldwide entity, with a variable spectrum of disease expression. Here in a case of paediatric Takayasu arteritis affecting purely the arch of aorta and it’s branches that was steroid resistant. DOI: http://dx.doi.org/10.3126/jnps.v33i2.7113 J Nepal Paediatr Soc. 2013; 33(2):144-146

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2

Rachid, L., W. Belkho, R. Zerhoudi, et al. "Syncope as Unexpected Presentation of Takayasu's Arteritis - A Case Report and Literature Review." Scholars Journal of Medical Case Reports 10, no. 3 (2022): 247–50. http://dx.doi.org/10.36347/sjmcr.2022.v10i03.020.

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Takayasu arteritis is an inflammatory disease that affects large vessels, especially the aorta and its branches. The clinical features of the disease depend on which arteries are affected.The syncope as uncommon presentation due to subclavian steal syndrome from Takayasu arteritis. We describe a case of a 36-year-old woman who presented with syncope and was found to have subclavian steal syndrome. We describe the patient’s hospital course leading to the diagnosis of TA, which is a rare form of vasculitis. Then, we discuss phases of Takayasu arteritis, explain the mechanism of syncope in this v

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3

Vahdatpour, Cyrus, Timothy Clark, and Harold Palevksy. "Endovascular treatment and long-term safety for pulmonary artery stenosis due to Takayasu’s arteritis – A case re port." American Journal of Interventional Radiology 8 (September 20, 2024): 14. http://dx.doi.org/10.25259/ajir_23_2024.

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Takayasu’s arteritis is a rare large vessel vasculitis which can involve the pulmonary arteries and progress to pulmonary artery (PA) stenosis with pulmonary hypertension. We present a case of Takayasu arteritis complicated by bilateral pulmonary stenosis and pulmonary hypertension that resolved after PA stenting and angioplasty. This case demonstrates the efficacy of endovascular intervention and sustained safety during 10 years of follow-up.

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4

Loetscher, Jonas, Susanna Fistarol, and Ulrich A. Walker. "Pyoderma Gangrenosum and Erythema Nodosum Revealing Takayasu’s Arteritis." Case Reports in Dermatology 8, no. 3 (2016): 354–57. http://dx.doi.org/10.1159/000452829.

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We report a Caucasian female who presented with simultaneous erythema nodosum and pyoderma gangrenosum due to underlying Takayasu’s arteritis. Takayasu’s arteritis is a chronic large vessel vasculitis of unknown cause. The disease has a worldwide distribution but is most commonly seen in Asian populations. There is a strong predilection for young females. The clinical presentation is variable, but mostly derives from stenosis or occlusion of affected arteries, resulting in claudication and ischemia. Skin manifestations are observed in up to 28% of patients with Takayasu’s arteritis, with eryth

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5

Shalini A, Srinivas V Y, and Nagashree J. Bharadwaj. "Anaesthetic management of a parturient with Takayasu’s arteritis coming for emergency caesarean section." Indian Journal of Clinical Anaesthesia 9, no. 1 (2022): 150–52. http://dx.doi.org/10.18231/j.ijca.2022.029.

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Takayasu’s arteritis (TA) also known as pulseless disease is a rare disease that involves aorta and its main branches. It can cause inflammatory reaction of tunica media and adventitia of the arteries involved causing stenosis, occlusion or aneurysm., Anaesthesia for caesarean section in a parturient with Takayasu’s arteritis is complicated by associated hypertension, end organ dysfunction, stenosis of major blood vessels and overall vasculopathy.The optimal anaesthetic management in a parturient with Takayasu’s arteritis is controversial, but avoidance of regional anaesthesia has been recomme

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6

Hall, Stephen, and Rachelle Buchbinder. "Takayasu’s Arteritis." Rheumatic Disease Clinics of North America 16, no. 2 (1990): 411–22. http://dx.doi.org/10.1016/s0889-857x(21)01066-8.

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7

Rajbhandari, Sujeeb. "Takayasu’s Arteritis." Nepalese Heart Journal 6, no. 1 (2017): 48–52. http://dx.doi.org/10.3126/njh.v6i1.18595.

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Takayasu’s arteritis is a disease of unknown etiology primarily affecting women aged less than 40 years. It is mainly seen in Asians and Africans. This condition is an aorto-arteritis and involves aorta and its major branches causing segmental narrowing or dilatation. Diminished or absent pulses and hypertension are common. Constitutional symptoms, including fever and weight loss, are often accompanied by elevation of acute phase markers. Diagnosis is made usually in quiescent or “cold phase” of the disease. Long-term complications are due mainly to arterial occlusion and related damage, inclu

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8

Qanadli, Salah D., Jean-François Sissakian, Paulo Rocha, Anne-Marie Piette, and Pascal Lacombe. "Takayasu’s Arteritis." Circulation 101, no. 3 (2000): 345–47. http://dx.doi.org/10.1161/01.cir.101.3.345.

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9

Sakaue, Saori, and Noboru Hagino. "Takayasu’s Arteritis." New England Journal of Medicine 375, no. 7 (2016): 675. http://dx.doi.org/10.1056/nejmicm1503040.

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10

Désiron, Q., and R. Zeaiter. "Takayasu’s Arteritis." Acta Chirurgica Belgica 100, no. 1 (2000): 1–6. http://dx.doi.org/10.1080/00015458.2000.12098506.

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11

Koening, Curry L., and Carol A. Langford. "Takayasu’s arteritis." Current Treatment Options in Cardiovascular Medicine 10, no. 2 (2008): 164–72. http://dx.doi.org/10.1007/s11936-008-0018-9.

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12

Mohan, Niveditha, and Gail Kerr. "Takayasu’s arteritis." Current Treatment Options in Cardiovascular Medicine 1, no. 1 (1999): 35–41. http://dx.doi.org/10.1007/s11936-999-0005-9.

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13

Fraga, Antonio, and Francisco Medina. "Takayasu’s arteritis." Current Rheumatology Reports 4, no. 1 (2002): 30–38. http://dx.doi.org/10.1007/s11926-002-0021-1.

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14

Akazawa, Hiroshi, Uichi Ikeda, Keiji Yamamoto, Toshio Kuroda, and Kazuyuki Shimada. "Hypercoagulable State in Patients with Takayasu’s Arteritis." Thrombosis and Haemostasis 75, no. 05 (1996): 712–16. http://dx.doi.org/10.1055/s-0038-1650353.

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SummaryThrombus formation is recognized pathologically in the affected arteries and is supposed to play a major role in the pathogenesis of Takayasu’s arteritis; however, hemostatic conditions in this disorder have not been elucidated fully. We determined plasma levels of molecular markers for platelet activity (platelet factor 4; PF4, β-throm-boglobulin; βTG), thrombotic status (thrombin-antithrombin III complex; TAT, fibrinopeptide A; FPA), fibrinolytic status (plasmin-β2-plasmin inhibitor complex; PIC, D-dimer), and endothelial injury (von Willebrand factor antigen; vWF:Ag, thrombomodulin;

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Aglave, Vikram, Shashank Nagendra, Pawan T. Ojha, et al. "Unusual etiology of stroke in young adults: think of Takayasu’s arteritis." International Journal of Advances in Medicine 8, no. 4 (2021): 594. http://dx.doi.org/10.18203/2349-3933.ijam20211061.

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Takayasu arteritis is an uncommon inflammatory disease of vessels that preferentially affects the aorta and its major branches. It can be a potential cause of stroke in young adults. Current study included 7 patients aged between 18 to 48 years. Each patient had varying presentations of stroke with Takayasu’s arteritis along with other neurological symptoms. Four of the 7 patients presented with ischemic strokes, one with hemorrhagic stroke, one with TIAs and one with syncopal attacks. All the patients had elevated erythrocyte sedimentation rates. Five of the seven patients were treated with s

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Ambiya, Vikas, Abhishek Kumar, Vijay K. Sharma, and Ashok Sharma. "Bilateral Takayasu’s retinopathy as the initial presentation of Takayasu’s arteritis." BMJ Case Reports 17, no. 4 (2024): e258688. http://dx.doi.org/10.1136/bcr-2023-258688.

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We present a case of Takayasu’s arteritis in a woman in her 30s, who exhibited visual symptoms and ophthalmic manifestations of the disease, specifically Takayasu’s retinopathy stage 4, in both eyes. Despite severe narrowing of all branches of the aortic arch and compromised perfusion in both upper limbs, she had no history of intermittent claudication. Doppler study and CT angiography revealed diffuse circumferential wall thickening of bilateral common carotid, subclavian and axillary arteries. Treatment involved retinal laser photocoagulation and immune suppression. This case underscores tha

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17

Virmani1, Mary, Luis Ortega, Loay Salman, Tushar Vachharajani, Arif Asif, and Ali Nayer. "Takayasu’s Arteritis: An Uncommon Cause of Renal Artery Stenosis and Therapeutic Considerations." Open Urology & Nephrology Journal 6, no. 1 (2013): 14–19. http://dx.doi.org/10.2174/1874303x01306010014.

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Takayasu’s arteritis is a rare disorder characterized by granulomatous and necro-inflammatory disease of the aorta and its major branches. Its etiology remains unknown. We report a young woman with Takayasu’s arteritis affecting the aortic arch, carotid, mesenteric, celiac and bilateral renal arteries resulting in severe hypertension, unilateral renal atrophy and renal insufficiency. The immunosuppressive therapy did not halt the progression of her vascular disease, which required revascularization procedures on numerous occasions. Here, the clinical manifestations and histopathological featur

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18

Singal, Kiran Kumar, Tejinder Talwar, Laxmikant Tanwar, Soumya Singh, Depali, and Bharat Veer. "Takayasu Arteritis Presenting As Congestive Cardiac Failure." International Journal of Human and Health Sciences (IJHHS) 3, no. 1 (2018): 37. http://dx.doi.org/10.31344/ijhhs.v3i1.73.

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Takayasu arteritis is a chronic systemic inflammatory disease that usualy affects the aorta, its primary branches and occasionaly the pulmonary and coronary arteries. The clinical manifestations vary considerably and are typicaly caused by limb or organ ischemia illness and fever. Occasionally, dyspnea and pedal edema can be the sole primary presentation of Takayasu’s arteritis.International Journal of Human and Health Sciences Vol. 03 No. 01 January’19. Page : 37-39

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Zhumaeva, Kh, O. Uraimov, A. Zhanbaeva, Zh Imetova, and Zh Abdullaeva. "Clinical Case in Takayasu Artery With Critical Lesion in Aortic Arch Branches (Takayasu’s Disease)." Bulletin of Science and Practice 7, no. 12 (2021): 122–26. http://dx.doi.org/10.33619/2414-2948/73/17.

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Research relevance: among Kyrgyz patients with Takayasu arteritis (AT), young women were predominated. The etiology is unknown. Research objectives: observation of the clinical manifestations in Takayasu’s arteritis in patients with the aim of compiling a diagnosis in treatment of disease. Research methods: most of patients had anatomical type V Takayasu arteritis (61.3%), vascular stage (89.3%) and severe stenosis (54.7%), lesions of the brachiocephalic trunk (68%), common sleepyheads (57.3%) and renal (52%) arteries. Severe exacerbation of the disease was observed in 82.7% of patients. The p

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20

Irpachi, Kalpana, Sandeep Sharan, Ameya Karanjkar, and Poonam Malhotra Kapoor. "Anesthesia Concerns in Child with Takayasu Arteritis for Catheterization Laboratory Intervention." Journal of Cardiac Critical Care TSS 03, no. 01 (2019): 49–50. http://dx.doi.org/10.1055/s-0039-1696908.

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AbstractTakayasu’s arteritis (pulse less disease) is a nonspecific chronic progressive panendarteritis affecting the large- and medium-sized arteries, involving the aorta and its main branches. Anesthesia for patients with Takayasu’s arteritis complicated by severe uncontrolled hypertension, end-organ dysfunction, stenosis of major blood vessels, and difficulties encountered in monitoring arterial blood pressure. We describe the anesthetic concerns of a child with Takayasu’s arteritis and severe hypertension refractory to medical treatment, presented with bilateral renal artery stenosis requir

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21

Hussain, Mohd Zahid, Md Tariqul Islam, Tahmina Karim, Shakhawat Alam, Mostafizur Rahman Bhuiyan, and Shima Bhadra. "Stenting in Takayasu’s Arteritis: A Case Report." Bangladesh Medical Research Council Bulletin 44, no. 2 (2018): 109–12. http://dx.doi.org/10.3329/bmrcb.v44i2.38706.

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Takayasu arteritis (TA), also known as idiopathic medial aortopathy or pulseless disease, is a granulomatous large vessel vasculitis that predominantly affects the aorta and its major branches. It may also affect the pulmonary arteries. The exact cause is not well known but the pathology is thought to be similar to giant cell arteritis. There is segmental and patch granulomatous inflammation of the aorta which results in stenosis, thrombosis and aneurysm formation. Half of the patients present with an initial systemic illness whereas the other 50% present with late-phase complications. There i

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22

Soto, María Elena, Claudia Huesca-Gómez, Yazmín Torres-Paz, Giovanny Fuentevilla-Álvarez, and Ricardo Gamboa. "Lack of Association between Cytokine Genetic Polymorphisms in Takayasu’s Arteritis in Mexican Patients." International Journal of Environmental Research and Public Health 16, no. 23 (2019): 4863. http://dx.doi.org/10.3390/ijerph16234863.

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Aim: To investigate the relation between polymorphisms in the interleukin 10 (IL)-10, tumor necrosis factor (TNF)-α, transforming growth factor (TGF)-β and interferon (IFN)-γ genes and Takayasu’s arteritis in the Mexican population. Methods: A case-control study was performed to investigate the associations of IL-10, TNF-α, TGF-β and IFN-γ polymorphisms in a sample of 52 Takayasu’s arteritis patients, diagnosed according to the criteria of the American College of Rheumatology and EULAR PRINTO criteria when the patients were under 18 years of age; 60 clinically healthy unrelated Mexican individ

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23

Jabed, Syed Md, Shaila Sharmin, Md Ferdous, and Puja Saha. "Takayasu Arteritis Presented with Unilateral Vision Loss : A Case Report." IAHS Medical Journal 6, no. 2 (2024): 90–92. http://dx.doi.org/10.3329/iahsmj.v6i2.76142.

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Background: Takayasu Arteritis (TA) is a rare chronic granulomatous inflammation of the aorta or its branches and is prevalent all around the world. It causes stenosis of large arteries and ischaemic damage to target organs. There is usually a delay in recognising TA because of the rarity and unfamiliarity with the disease, unspecific early symptoms and lack of diagnostic equipment for early diagnosis. The purpose of the study to reminding readers of this issue and emphasize the necessity for further research on how to deal with in the best way. Case Report: We report a case of 30 years old ma

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Aziz, Ahmad Monjurul, Rubina Yasmin, Md Azharul Haque, and Dilruba Yeasmin. "Takayasu’s Arteritis- A Review." Journal of Bangladesh College of Physicians and Surgeons 38, no. 1 (2019): 35–45. http://dx.doi.org/10.3329/jbcps.v38i1.44687.

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Takayasu’s arteritis (TA) is a rare, idiopathic, chronic inflammatory disease with cell-mediated inflammation, involving mainly the aorta and its major branches. It leads to stenosis, occlusion or aneurysmal degeneration of large arteries. The clinical presentation is characterized by an acute phase with constitutional symptoms, followed, months or years later, by a chronic phase in which symptoms relate to fibrosis or occlusion of vessels. Conventional angiography, the gold standard method for initial diagnosis, appears to have been replaced with new imaging modalities such as magnetic resona

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25

Shrestha, Gentle Sunder, Ninadini Shrestha, Battu Kumar Shrestha, and Pramesh Sunder Shrestha. "Anaesthetic Management of Patients with Takayasu’s Arteritis for Open Cholecystectomy: a Report of Two Cases." Journal of Nepal Medical Association 53, no. 198 (2015): 146–49. http://dx.doi.org/10.31729/jnma.2779.

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Takayasu’s arteritis is a well known yet rare form of large vessel vasculitis. This inflammatory disease often affects the ascending aorta and aortic arch, causing obstruction of the aorta and its major arteries. Anaesthetic management for these patients is complicated by severe hypertension, end-organ dysfunction, stenosis of major blood vessles and difficulties in monitoring blood pressure. We present two patients who underwent open cholecystectomy under neuraxial anaesthesia. We have discussed about various perioperative issues and their management. Keywords: anaesthetic management; t

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Pulak, Sadriye, İnan Anaforoğlu, Şakir Özgür Keşkek, krem Algün, and Esin Ertuğrul. "A Takayasu arteritis case presented with pulmonary involvement in a male patient with diabetic foot ulcers: Case report." Journal of Medical Research 2, no. 4 (2016): 88–90. http://dx.doi.org/10.31254/jmr.2016.2402.

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Takayasu’s arteritis is a rare form of chronic systemic vasculitis. It predominantly affects young adults, women in particular. We report an unusual case of Takayasu’s arteritis with pulmonary involvement in a 47-year-old male patient with diabetic foot ulcers. Patient was admitted to the hospital with high blood sugar, unhealed foot ulcers, weakness and weight loss. He developed sudden dyspnea during the treatment. The diagnosis of Takayasu’s arteritis was made using physical examination and computed tomography angiography.

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Sharma, Pallav K., Chandan Kumar, and Suraj Kumar. "Beyond the pulse: unusual presentations of Takayasu’s arteritis." International Journal of Research in Medical Sciences 12, no. 8 (2024): 3033–35. http://dx.doi.org/10.18203/2320-6012.ijrms20242239.

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Takayasu’s arteritis (TA) a.k.a pulseless disease is a chronic inflammatory occlusive thrombo-aortopathy. It is a rare inflammatory disease affecting large arteries, often leading to significant diagnostic challenges, especially when presenting with atypical symptoms. This case report explores a patient, whose primary complaints were chest pain and no neurological or constitutional symptoms, diverging from the common presentations of diminished pulses or limb claudication. Advanced imaging, including CT Aortogram and interventions like cardiac angiography, played a crucial role in detecting va

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Mastrogiuseppe, Elvia, Maria Pia Pirraglia, Lorenzo Sampalmieri, Ludovico Iannetti, Alessandro Beccia, and Magda Gharbiya. "Management of Spontaneous Crystalline Lens Luxation in a Patient Diagnosed with Takayasu’s Disease." Diagnostics 13, no. 8 (2023): 1400. http://dx.doi.org/10.3390/diagnostics13081400.

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Takayasu’s disease is a chronic granulomatous arteriopathy that affects large vessels and their major branches. Nonspecific symptoms characterize the early phase, whereas findings of arterial occlusion and aneurysmal formation become manifest later. Ocular signs typically refer to retinal vascular involvement, as Takayasu arteritis or hypertensive retinopathy. We report a case of a 63-year-old woman suffering from Takayasu arteritis that complained of sudden onset of blurred vision in her left eye due to crystalline lens luxation in the vitreous cavity. The patient’s past medical history was u

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Moisii, Paloma, Irina Jari, Alexandru Gratian Naum, Doina Butcovan, and Grigore Tinica. "Takayasu’s Arteritis: A Special Case Report and Review of the Literature." Medicina 60, no. 3 (2024): 456. http://dx.doi.org/10.3390/medicina60030456.

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Background: Takayasu’s arteritis is a rare type of vasculitis with severe complications like stroke, ischemic heart disease, pulmonary hypertension, secondary hypertension, and aneurysms. Diagnosis is achieved using clinical and angiographic criteria. Treatment is medical and surgical, but unfortunately, the outcome is limited. Case presentation: A 34-year-old Caucasian woman had an ischemic stroke (2009). She was diagnosed with Takayasu’s arteritis and received treatment with methotrexate, prednisolone, and antiplatelet agents, with a mild improvement in clinical state. After 6 years (2015),

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Reddy, Srikrishna Modugula, and Srinivas Pallikala Reddy. "Stenosis of the main stem of the left coronary artery in a teenager with Takayasu’s Arteritis." Cardiology in the Young 19, no. 6 (2009): 638–40. http://dx.doi.org/10.1017/s1047951109990886.

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AbstractCoronary arterial involvement is rare in Takayasu’s arteritis. We describe successful coronary arterial bypass grafting in a 15 year teenager with Takayasu’s arteritis and unstable angina because of stenosis of the main stem of the left coronary artery.

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Ferraz de Freitas, Marcelo, Marcelo Valladão de Carvalho, and Marcelo Derbli Schafranski. "Association of aortic and main left coronary aneurysms with severe aortic insufficiency in Takayasu’s arteritis." Clinics and Practice 1, no. 2 (2011): 26. http://dx.doi.org/10.4081/cp.2011.e26.

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Takayasu’s arteritis is a granulomatous vasculitis of unknown etiology that affects mainly the aorta and its branches. As a result of intimal fibroproliferation, segmental stenosis, occlusion, dilatation, and aneurysmal formation of the involved vessels may develop. It is an uncommon disease and usually affects young Asian female patients during the second and third decades of life. Coronary arteries are exceptionally affected and coronary aneurysm formation is a very rare finding. We describe a case of a previously healthy 26-year-old Caucasian female whose Takayasu’s arteritis presented as a

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Mustafa, Khader N. "Takayasu’s arteritis in Arabs." Clinical Rheumatology 33, no. 12 (2014): 1777–83. http://dx.doi.org/10.1007/s10067-014-2633-z.

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Alnajjar, A., A. Hegazy, and N. Al Ghanim. "THU0588 TAKAYASU’S ARTERITIS PRESENTING WITH UNILATERAL DIGITAL CLUBBING IN A 23 YEAR-OLD MALE." Annals of the Rheumatic Diseases 79, Suppl 1 (2020): 536. http://dx.doi.org/10.1136/annrheumdis-2020-eular.3859.

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Background:Takayasu Arteritis is a chronic, large vessel arteritis that commonly involves the aorta and its major branches, mostly the ascending/descending aorta, subclavian arteries, and carotids [1].Herein, we report a case of a 23 year-old medically free Indian male who presented to our hospital in acute distress complaining of cough, hemoptysis and shortness of breath for one week as well as intermittent fever and fatigue for five months. He presented with a BP of 140/100 mmHg as well was both systolic and early diastolic murmurs in the mitral and aortic areas, respectively. He also had a

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Gupta, Vinita, Saurabh Luthra, N. Shrinkhal, and Sony Sinha. "Takayasu’s arteritis: a unique ophthalmic presentation with CRAO and BRVO." BMJ Case Reports 12, no. 8 (2019): e228909. http://dx.doi.org/10.1136/bcr-2018-228909.

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A unique case of sequential occurrence of central retinal artery occlusion (CRAO) and superotemporal branch retinal vein occlusion (ST-BRVO) in a patient of Takayasu’s arteritis is described. An 18-year-old man was diagnosed as left eye CRAO on his initial presentation and was subjected to a complete cardiovascular evaluation revealing findings diagnostic of Takayasu’s arteritis. Patient was however lost to follow-up and presented 16 months later with ST-BRVO in the right eye. Multidisciplinary intervention and an appropriate ocular intervention led to complete recovery of vision in the right

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Biswas, Sarmistha, SM Hafiz, Kamalesh Chandra Basu, AHM Ejrarul Alam Khan, Mouri Sarker, and Tanveer Ahmed. "Systemic Lupus Erythematosus with Takayasu’s Arteritis - A Rare Co-existance." Journal of Medicine 22, no. 2 (2021): 146–49. http://dx.doi.org/10.3329/jom.v22i2.56706.

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We report the case of a 30-year-old normotensive, nondiabetic lady diagnosed case of Systemic Lupus Erythematosus(SLE); who came with the complaints of limb claudication. After clinical and lab evaluation she was diagnosed as a case of Takayasus Arteritis along with SLE. Though the co- existence of SLE and Takayasu’s Disease is very rare, we should search for the development of arterial occlusive diseases in SLE cases if the patient has got suspicious symptoms. J MEDICINE 2021; 22: 146-149

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Abrahan, Lauro L., Elleen L. Cunanan, Percy Jun G. Prieto, Jaime Alfonso M. Aherrera, Antonio L. Faltado, and Maria Teresa B. Abola. "Renal Artery Stenosis in Takayasu’s Arteritis Causing Early-Onset Hypertension: A Report of Four Cases at the UP-Philippine General Hospital." Philippine Journal of Cardiology 44, no. 2 (2016): 61–70. http://dx.doi.org/10.69944/pjc.928b2e6118.

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Background: In foreign literature, 90% of renal artery stenosis (RAS) is atherosclerotic, while 10% is secondary to fibromuscular dysplasia (FMD). However, an important differential for hypertension in the young Asian population is Takayasu’s arteritis. We present four patients who initially presented with hypertension in the young due to RAS. Clinical criteria coupled with non-invasive studies in all four cases led to the diagnosis of Takayasu’s arteritis. All four patients had good outcomes. Case: Four patients (one male and three females) all presented with early-onset hypertension in the t

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Basek, I. V., and N. N. Berezkina. "THE ROLE OF MDCT ANGOIGRAPHY IN THE DIAGNOSIS OF TAKAYASU ARTERITIS. CASE REPORT." Translational Medicine 5, no. 6 (2019): 51–57. http://dx.doi.org/10.18705/2311-4495-2018-5-6-51-57.

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Takayasu’s disease (non-specific aorto-arteritis) is a chronic, idiopathic, inflammatory disease that primarily affects large vessels, such as the aorta and its major branches, including the pulmonary and coronary arteries. It often develops in women under the age of 50 years. Accurate and early diagnosis plays an important role in the prognosis of life in patients with this pathology. Complaints of patients with lesions of the aorta and its branches are non-specific in nature and are characterized by fever, night sweats, malaise and arthralgia, passing under the “mask” of other diseases. With

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Rawal, S. "Mortality in a second gravida following dissecting aortic aneurysm due to Takayasu’s Arteritis." Journal of Institute of Medicine Nepal 29, no. 2 (2007): 46–49. http://dx.doi.org/10.59779/jiomnepal.294.

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Takayasu’s arteritis is a vasculitis involving the aorta and its branches. This is a case of undiagnosed Takayasu’s arteritis in a 32 weeks pregnant lady, who presented to the emergency department with complaints of severe chest and epigastric pain and signs consistent with aortic aneurysm. The woman died of aortic dissection two days later.

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Sirohi, Parmendra, Peeyush Sharma, Rahul Gupta, and Manaswi Vishwakarma. "Vasculitis masquerading as a mass: a case report of Takayasu arteritis in a 28-year-old male." International Journal of Research in Medical Sciences 12, no. 6 (2024): 2157–59. http://dx.doi.org/10.18203/2320-6012.ijrms20241581.

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Takayasu arteritis is a chronic vasculitis mainly involving the aorta and its main branches most commonly subclavian and carotid. It induces clinically varied ischaemic symptoms due to stenotic lesions or thrombus formation, including blindness, retinal haemorrhage, pulselessness, aortic regurgitation and congestive heart failure due to dilatation of the ascending aorta. More acute progression causes destruction of arterial wall, leading to the formation of aneurysms and rupture of the involved arteries. Here we present a case of Takayasu’s arteritis in a 28-year-old male who presented with no

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Petrov, A. V., A. A. Zayaeva, J. V. Usachenko, et al. "Difficulties in the Diagnosis and Management of Patients with Takayasu’s Arteritis: A Description of a 5-Year Clinical Follow-Up." Russian Archives of Internal Medicine 13, no. 5 (2023): 377–84. http://dx.doi.org/10.20514/2226-6704-2023-13-5-377-384.

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Takayasu’s disease (nonspecific aortoarteritis) is a granulomatous inflammation of the aorta and its main branches with a progressive course and development of severe ischemic disorders. The difficulty of diagnosis and the possibility of applying various methods of pathogenetic anti-inflammatory treatment of Takayasu’s arteritis make it expedient to study a clinical case. The analysis of a clinical case of a patient with Takayasu’s arteritis with manifestation of the disease in the form of general inflammatory syndrome and manifestations of severe cerebral ischemia due to bilateral stenotic ca

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Verma, Ashish, Ishan Kumar, Priyanka Aggarwal, and Ram C. Shukla. "Imaging Spectrum of Pediatric Nonspecific Aortoarteritis on CT Angiography: A Retrospective Study." Annals of the National Academy of Medical Sciences (India) 55, no. 03 (2019): 145–50. http://dx.doi.org/10.1055/s-0039-1697238.

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Abstract Introduction Takayasu’s arteritis, a chronic, idiopathic, inflammatory panarteritis, is the major cause of Aortoarteritis in pediatric age group. The purpose of this study is to analyze the patterns of involvement and imaging findings of pediatric Takayasu’s arteritis. Materials and Methods We retrospectively reviewed the CT angiographic images of 11 pediatric cases reported as “Takayasu’s arteritis” or “nonspecific arteritis” over the period of last 3 years. Results Mural thickening with luminal stenosis was the most common findings. Aneurysmal dilatation of the descending thoracic a

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Wang, L., Y. Sun, X. Dai, et al. "POS0812 CAROTID INTIMA-MEDIA THICKNESS/DIAMETER RATIO AND PEAK SYSTOLIC VELOCITY AS RISK FACTORS FOR NEUROLOGICAL SEVERE ISCHEMIC EVENTS IN TAKAYASU’S ARTERITIS." Annals of the Rheumatic Diseases 81, Suppl 1 (2022): 695.2–696. http://dx.doi.org/10.1136/annrheumdis-2022-eular.3666.

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BackgroundTakayasu’s arteritis (TAK) is an idiopathic systemic vasculitis characterized by the involvement of the aorta and its major branches [1]. The supra-aortic arteries are often involved in TAK, with the reported prevalence ranging from 40% to 84% [2-3]. Importantly, patients with supra-aortic involvement carry a higher risk of neurological severe ischemic events (SIE) [4-5]. The common carotid artery (CCA) is the most affected artery and is more closely associated with neurologic symptoms than other supra-aortic arteries [6]. Ultrasonography (US) has been regarded as the most popular, u

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Mohan, Sharmila, and R. Lakshmi. "A CASE REPORT ON TAKAYASU’S ARTERITIS." International Journal of Pharmacy and Pharmaceutical Sciences 9, no. 3 (2017): 296. http://dx.doi.org/10.22159/ijpps.2017v9i3.15034.

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Takayasu’s arteritis (TA) is a rare large-vessel vasculitis that affects large arteries, mainly the aorta and its branches. It is also called a pulseless disease because of diminished or absent pulses in the upper extremities of the patient. The coronary, pulmonary and renal arteries are also affected in the progression of the disease. The prevalence of the disease is more in Asian countries and it has unknown etiopathogenesis. Here we discuss a case of TA in a 15 y old girl who was admitted with moderate LV dysfunction. The diagnosis was carried out from the results of CT aortogram which show

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Pörings, Anna Sophia, Bernd Salzberger, Lothar Veits, Boris Ehrenstein, Wolfgang Hartung, and Martin Fleck. "Syphilitic Aortitis Mimicking Takayasu’s Arteritis." Case Reports in Clinical Medicine 03, no. 08 (2014): 457–59. http://dx.doi.org/10.4236/crcm.2014.38100.

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Johnson, Andrea, Derek Emery, and Alison Clifford. "Intracranial Involvement in Takayasu’s Arteritis." Diagnostics 11, no. 11 (2021): 1997. http://dx.doi.org/10.3390/diagnostics11111997.

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Takayasu’s arteritis (TAK) is a large-vessel vasculitis that targets the aorta and its major branches. Although extracranial vascular involvement is uniformly present in this disease, the frequency of intracranial involvement in TAK has not been well studied. We retrospectively reviewed the clinical and imaging records of patients diagnosed with TAK at a single Canadian university medical centre to determine the prevalence of intracranial vascular involvement. Intracranial vascular and non-vascular findings were described, and a review of the literature was performed. Of 20 patients with TAK,

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Hoffman, Gary S. "TREATMENT OF RESISTANT TAKAYASU’S ARTERITIS." Rheumatic Disease Clinics of North America 21, no. 1 (1995): 73–80. http://dx.doi.org/10.1016/s0889-857x(21)00371-9.

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Gupta, Avinash, Divya Bagoria, Jaya Pamnani, and Sumitra Choudhary. "CASE REPORT OF TAKAYASU’S ARTERITIS." Journal of Evidence Based Medicine and Healthcare 3, no. 44 (2016): 2232–35. http://dx.doi.org/10.18410/jebmh/2016/494.

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Matsumura, Yoshihisa, Keisuke Morimoto, Mitsuko Ishikawa, Hiroaki Kitaoka, and Yoshinori L. Doi. "Ultrasonographic Images of Takayasu’s Arteritis." Circulation 98, no. 15 (1998): 1585–86. http://dx.doi.org/10.1161/01.cir.98.15.1585.

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Al-Bishri, J. "Takayasu’s Arteritis: A Review Article." British Journal of Medicine and Medical Research 3, no. 4 (2013): 811–20. http://dx.doi.org/10.9734/bjmmr/2013/3150.

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Yoshikawa, Yasuji, and Luan D. Truong. "Membranoproliferative Glomerulonephritis in Takayasu’s Arteritis." Nephron 57, no. 4 (1991): 497. http://dx.doi.org/10.1159/000186363.

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