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Relevant bibliographies by topics / Takayasu’s arteritis

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Academic literature on the topic 'Takayasu’s arteritis'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Takayasu’s arteritis"

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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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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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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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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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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Dissertations / Theses on the topic "Takayasu’s arteritis"

1

Schmidt, Wolfgang Andreas. "Duplex-Sonographie in der Diagnostik der Arteriitis temporalis und anderer Vaskulitiden." Doctoral thesis, [S.l.] : [s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=964532360.

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Currer, Trevor H. "Non-specific aortic arteritis (Takayasu's disease) : the Cape Town experience." Master's thesis, University of Cape Town, 1989. http://hdl.handle.net/11427/25686.

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Non-specific aortic arteritis remains a disease of unknown aetiology, in which the treatment is empiric, the indications for surgery controversial and the prognosis unpredictable. Most series emanate from the Far East, with few contributions from Africa. The pattern of disease as seen in-Cape Town has not been documented since the study of Schrire and Asherson in 1964, containing 18 cases. In this study at Groote Schuur and Red Cross Children's Hospital from 1952 to 1987, only patients who had been extensively investigated and subjected to angiography were included. strict· inclusion criteria

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Silva, Thiago Ferreira da. "Avaliação da síndrome metabólica em pacientes com arterite de Takayasu." Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/5/5166/tde-10122013-105453/.

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Introdução: A prevalência de Síndrome Metabólica (SM) tende a ser alta em pacientes com doenças reumáticas, sendo as doenças cardiovasculares a principal causa de óbito nestas condições. Objetivos: Determinar a prevalência de SM em pacientes com Arterite de Takayasu (AT) e sua associação com fatores de risco, níveis de adipocinas e de citocinas. Métodos: Foi realizado um estudo transversal incluindo 45 mulheres com AT e 47 controles saudáveis pareados por idade e índice de massa corporal (IMC). Resultados: A prevalência de SM (critérios da IDF/AHA) foi maior em pacientes com AT comparada aos c

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Baptista, Luciana de Padua Silva. "Contribuição da ressonância magnética na arterite de Takayasu." Universidade de São Paulo, 2007. http://www.teses.usp.br/teses/disponiveis/5/5151/tde-19032007-111701/.

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Introdução: Os critérios diagnósticos da arterite de Takayasu (AT) se baseiam em alterações do lúmen vascular, detectadas pela angiografia convencional (AC). Além das lesões do lúmen, as alterações na parede da aorta, caracterizadas pela ressonância magnética (RM), estão sempre presentes na AT, não sendo demonstradas pela AC. Objetivos: Descrever as lesões do lúmen da aorta e seus ramos e as alterações na parede da aorta por RM, em pacientes com AT, estabelecendo a associação entre os achados de imagem da aorta e atividade da doença. Métodos: A amostra compreendeu 45 pacientes (43 brancos, 40

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Oliveira, Diego Sales de. "Efeitos agudos e crônicos do exercício físico aeróbio em pacientes com arterite de Takayasu." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/5/5164/tde-06092016-161452/.

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Introdução: A arterite de Takayasu (AT) é uma vasculite sistêmica rara caracterizada por oclusão, ectasias, aneurismas e estenose da aorta e seus ramos principais. Consequentemente, pode levar a uma redução no pulso de uma ou mais artérias, diferença nos níveis de pressão sistólica dos membros, presença de sopros (cervicais, cardíacos, axilares e/ou abdominais), além da presença de claudicação vascular (membros e/ou vísceras abdominais) e isquemia periférica, o que por sua vez pode levar a uma maior limitação funcional e consequentemente ao sedentarismo. Esses acometimentos podem, em última an

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Mont\'Alverne, Andrea Rocha de Saboia. "Redução da reserva ovariana em pacientes com artrite de Takayasu." Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/5/5164/tde-01042016-151824/.

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Objetivo: Avaliar marcadores de reserva ovariana e a presença de anticorpo anti-corpo lúteo (anti-CoL) em pacientes com arterite de Takayasu (AT) e possível associação com parâmetros clínicos, laboratoriais e uso de imunossupressores. Métodos: 20 pacientes com AT e 24 controles saudáveis foram avaliados para anti-CoL (immunoblot). A reserva ovariana foi avaliada por: hormônio folículo estimulante (FSH), hormônio luteinizante (LH), estradiol, hormônio anti-Mülleriano (HAM) e contagem de folículos antrais (CFA). HAM foi dosado por ELISA utilizando dois diferentes testes. Dados demográficos, obst

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Godoy, Carrillo María Claudia, Saco Alejandra Meneses, C. Víctor Torrealva, and A. César Pastor. "Nefropatía por poliomavirus en un paciente inmunosuprimido por trasplante renal secundario a la enfermedad de arteritis de Takayasu." Elsevier B.V, 2016. http://hdl.handle.net/10757/604547.

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Polyomavirus nephropathy is a disease that predominates in renal transplant patients due to the immunosuppressive treatment for the maintenance of the renal graft. The current prevalence of this disease ranges between 1-14%. The suspicion of the disease comes from the presence of decoy cells in urine samples and the gold standard for the diagnosis is the presence of viral inclusions in the renal biopsy. In this case report, we describe a patient with a renal transplant secondary to Takayasu arteritis who presented renal failure evidenced by progressive elevation of serum creatinine. The renal

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Fritsch, Scheila. "Tradução e validação do escore indiano de atividade clínica da arterite de Takayasu em língua portuguesa." reponame:Repositório Institucional da UFPR, 2017. http://hdl.handle.net/1884/49382.

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Orientador : Prof. Dr. Valderílio Feijó Azevedo<br>Coorientador : Prof. Dr. Alexandre Wagner Silva de Souza<br>Dissertação (mestrado) - Universidade Federal do Paraná, Setor de Ciências da Saúde, Programa de Pós-Graduação em Medicina Interna. Defesa : Curitiba, 07/08/2017<br>Inclui referências : f. 45-49<br>Resumo: Introdução: A Arterite de Takayasu é uma vasculite sistêmica que ocasiona inflamação parietal de grandes artérias. Em 2010, surgiu um questionário clínico com objetivo de melhorar a avaliação clínica e definições terapêuticas, o ITAS2010 - Indian Takayasu's Arteritis Activity Score.

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Neto, Nilton Salles Rosa. "Avaliação não invasiva das propriedades estruturais de grandes artérias em pacientes com arterite de Takayasu." Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/5/5164/tde-16092013-151428/.

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A Arterite de Takayasu (AT) é uma vasculite granulomatosa de aorta e grandes vasos associada a elevado risco cardiovascular. A velocidade de onda de pulso (VOP) é um método de avaliação indireta de diminuição da distensibilidade arterial, e valores elevados de VOP correlacionam-se com maior morbimortalidade cardiovascular. A avaliação da VOP em pacientes com arterite de Takayasu é complexa devido a muitos fatores de confusão. O objetivo do presente estudo foi avaliar a rigidez arterial, por meio da velocidade de onda de pulso carótido-femoral (VOP-CF) em pacientes do sexo feminino com arterite

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Nakajima, Toshiki. "A novel susceptibility locus in the IL12B region is associated with the pathophysiology of Takayasu arteritis through IL-12p40 and IL-12p70 production." Kyoto University, 2018. http://hdl.handle.net/2433/231011.

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Books on the topic "Takayasu’s arteritis"

1

Malan, Gandhi, ed. Non-specific aorto-arteritis (takayasu's disease): Pathology and radiology. Quest Publications, 1998.

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2

Katritsis, Demosthenes G., Bernard J. Gersh, and A. John Camm. Inflammatory diseases associated with thoracic aortic disease. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199685288.003.1676.

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Sprynger, Muriel, Iana Simova, and Scipione Carerj. Vascular echo imaging. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198726012.003.0068.

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Arterial diseases are heavily intertwined with atherosclerosis and coronary artery disease and the presence of both symptomatic and asymptomatic peripheral artery diseases is known to affect the rate of cardiovascular events and deaths. Screening for abdominal aortic aneurysm (AAA) in selected populations is also a major issue for the cardiologist. Additionally, intima-media thickness and ankle-brachial index (ABI) measurements, screening for carotid or femoral plaques, and new techniques looking at the rigidity and elasticity of arteries may further help with risk stratification, especially i

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TYAGI, R. O. Y. Takayasu Arteritis Hb: Takayasu Arteritis. Jaypee Brothers Medical Publishers, 2023.

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Pipitone, Nicolò, Annibale Versari, and Carlo Salvarani. Large-vessel vasculitis. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199642489.003.0133_update_003.

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Large-vessel vasculitis includes giant cell arteritis (GCA) and Takayasu’s arteritis (TAK). GCA affects patients aged over 50, mainly of white European ethnicity. GCA occurs together with polymyalgia rheumatica (PMR) more frequently than expected by chance. In both conditions, females are affected two to three times more often than males. GCA mainly involves large- and medium-sized arteries, particularly the branches of the proximal aorta including the temporal arteries. Vasculitic involvement results in the typical manifestations of GCA including temporal headache, jaw claudication, and visua

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Prettyman, Mamie. Coloring Book - You Will Get Better - Takayasu's Arteritis: Heal While Coloring. Independently Published, 2021.

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Michet, Clement J., Kenneth G. Moder, and William W. Ginsburg. Rheumatology. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780199755691.003.0681.

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Major rheumatologic diseases are reviewed in detail, including symptoms, diagnosis, and treatment. Rheumatoid arthritis, Sjogren syndrome, Felty syndrome, osteoarthritis, fibromyalgia, and vasculitic syndromes like giant cell arteritis, polyarteritis nodosa, Takayasu arteritis, and Wegener granulomatosis are included. Drugs used to treat rheumatic disease are also highlighted. They include NSAIDs, antimalarials, and glucocorticosteroids. Crystalline arthropathies, such as hyperuricemia and gout, are another class of rheumatologic disease, as are spondyloarthropathies, systemic lupus erythemato

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Pipitone, Nicolò, Annibale Versari, and Carlo Salvarani. Large-vessel vasculitis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0133.

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Large-vessel vasculitis includes giant cell arteritis (GCA) and Takayasu's arteritis (TAK). GCA affects patients aged over 50, mainly of white European ethnicity. GCA occurs together with polymyalgia rheumatica (PMR) more frequently than expected by chance. In both conditions, females are affected two to three times more often than males. GCA mainly involves large- and medium-sized arteries, particularly the branches of the proximal aorta including the temporal arteries. Vasculitic involvement results in the typical manifestations of GCA including temporal headache, jaw claudication, and visua

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Foster, Brogan, and Paul A. Brogan. Systemic diseases. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198738756.003.0004.

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This chapter covers the full spectrum of systemic diseases in paediatric rheumatology including: the systemic vasculitides (HSP, Kawasaki disease, PAN, ANCA-associated vasculitis, Takayasu arteritis, Behçet's disease, cerebral vasculitis, and many others); juvenile SLE; scleroderma; JDM; overlap syndromes; antiphospholipid syndrome; sarcoid; and paediatric uveitis. In addition, it provides updated descriptions and treatment approaches for autoinflammatory diseases, including recently described diseases such as DADA, SAVI, CANDLE, and many others. Other systemic diseases described in detail inc

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Ritchie, James, Darren Green, Constantina Chrysochou, and Philip A. Kalra. Renal artery stenosis. Edited by Neil Turner. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0213.

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Renovascular disease refers to a narrowing of a main or branch renal artery. Consequences include loss of functional renal tissue and renovascular hypertension, with other manifestations depending on the underlying cause. Worldwide the most common cause is atherosclerotic narrowing, with other causal pathologies including fibromuscular disease (FMD) and inflammatory conditions. FMD occurs much more frequently in women than in men, and is associated with smoking but genetic predisposing factors are also suspected. In South East Asia, Takayasu arteritis is an important cause.Takayasu disease oft

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Book chapters on the topic "Takayasu’s arteritis"

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Todua, Fridon, and Dudana Gachechiladze. "Takayasu’s Arteritis." In Noninvasive Radiologic Diagnosis of Extracranial Vascular Pathologies. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-91367-4_15.

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Cao, Jian, Yining Wang, and Zheng-yu Jin. "Takayasu’s Arteritis." In Cardiac CT. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-5305-9_8.

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Shek, Yilin, and Shlee S. Song. "Takayasu’s Arteritis." In Carotid Artery Disease. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-41138-1_16.

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Quinn, Kaitlin A., Durga P. Misra, Aman Sharma, Andrew Porter, Justin Mason, and Peter C. Grayson. "Takayasu’s Arteritis." In A Clinician's Pearls & Myths in Rheumatology. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-23488-0_28.

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Raj, Satish R., S. R. Wayne Chen, Robert S. Sheldon, et al. "Takayasu’s Arteritis." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_8108.

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Vaideeswar, Pradeep. "Childhood Takayasu’s Arteritis." In Tropical Cardiovascular Pathology. Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-3720-0_63.

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Jha, Avanish, and Debashish Danda. "Biologics in Takayasu’s Arteritis." In Handbook of Biologics for Rheumatological Disorders. Springer Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-7200-2_12.

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Kim, Hyun Jung, and Dae Chul Suh. "Endovascular Treatment of Takayasu’s Arteritis." In Endovascular Interventions. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7312-1_71.

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Silva, Christian Espinoza, Diego Soto Valdés, and Vania Rozas Almeida. "Management of Aneurysms in Takayasu’s Arteritis." In Inflammatory Response in Cardiovascular Surgery. Springer London, 2013. http://dx.doi.org/10.1007/978-1-4471-4429-8_23.

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Kim, Duk-Kyung, and Young-Wook Kim. "Takayasu’s Arteritis Associated with Cerebrovascular Ischemia." In Vascular Surgery. Springer London, 2010. http://dx.doi.org/10.1007/978-1-84996-356-5_35.

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Conference papers on the topic "Takayasu’s arteritis"

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CRACCO, LUIZ AUGUSTO FANHANI, Fabio Henrique Carneiro, André Wilson de Lima Oliveira, et al. "Takayasu’s arteritis with uveitis." In XXXIX Congresso Brasileiro de Reumatologia. Sociedade Brasileiro de Reumatologia, 2022. http://dx.doi.org/10.47660/cbr.2022.1934.

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Tomelleri, Alessandro, Corrado Campochiaro, Silvia Sartorelli, Veronica Bandini, Elena Baldissera, and Lorenzo Dagna. "THU0319 TAKAYASU’S ARTERITIS: BEYOND THE VESSELS." In Annual European Congress of Rheumatology, EULAR 2019, Madrid, 12–15 June 2019. BMJ Publishing Group Ltd and European League Against Rheumatism, 2019. http://dx.doi.org/10.1136/annrheumdis-2019-eular.953.

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Kimyon, U., S. N. Esatoglu, E. Kara, et al. "SAT0546 Sensorineural hearing loss in takayasu’s arteritis." In Annual European Congress of Rheumatology, EULAR 2018, Amsterdam, 13–16 June 2018. BMJ Publishing Group Ltd and European League Against Rheumatism, 2018. http://dx.doi.org/10.1136/annrheumdis-2018-eular.2962.

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Sequeira, G., F. Saraiva, A. Marques, J. Romeu, T. Costa, and V. Queiroz. "AB0087 Takayasu’s arteritis: review and four clinical cases." In Annual European Congress of Rheumatology, Annals of the rheumatic diseases ARD July 2001. BMJ Publishing Group Ltd and European League Against Rheumatism, 2001. http://dx.doi.org/10.1136/annrheumdis-2001.194.

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Singh, J., and R. Brasington. "AB0091 Pulmonary takayasu’s arteritis mimicking acute pulmonary embolism." In Annual European Congress of Rheumatology, Annals of the rheumatic diseases ARD July 2001. BMJ Publishing Group Ltd and European League Against Rheumatism, 2001. http://dx.doi.org/10.1136/annrheumdis-2001.198.

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lorenzoni Grillo, Luiza, Debora Marques Veghini, Anna Carolina Simões Moulin, et al. "TAKAYASU’S ARTERITIS ASSOCIATED TO MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS: A CASE REPORT." In SBR 2021 Congresso Brasileiro de Reumatologia. Sociedade Brasileira de Reumatologia, 2021. http://dx.doi.org/10.47660/cbr.2021.2164.

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Tent, Michiel. "Mycophenolate mofetil plus methotrexate is effective in Takayasu’s arteritis." In ACR Convergence 2024, edited by Dennis McGonagle. Medicom Medical Publishers, 2025. https://doi.org/10.55788/e780327c.

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Du, J. "AB0674 Risk factors of atherosclerosis in patients with takayasu’s arteritis." In Annual European Congress of Rheumatology, EULAR 2018, Amsterdam, 13–16 June 2018. BMJ Publishing Group Ltd and European League Against Rheumatism, 2018. http://dx.doi.org/10.1136/annrheumdis-2018-eular.3300.

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Kilic, L., O. Karadag, A. Erden, et al. "THU0452 Anti-interleukin-6 (TOCILIZUMAB) experience in takayasu’s arteritis patients." In Annual European Congress of Rheumatology, EULAR 2018, Amsterdam, 13–16 June 2018. BMJ Publishing Group Ltd and European League Against Rheumatism, 2018. http://dx.doi.org/10.1136/annrheumdis-2018-eular.6756.

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Korkmaz, C. "AB0075 Aortitis syndrome (takayasu’s arteritis) associated with systemic lupus erythematosus." In Annual European Congress of Rheumatology, Annals of the rheumatic diseases ARD July 2001. BMJ Publishing Group Ltd and European League Against Rheumatism, 2001. http://dx.doi.org/10.1136/annrheumdis-2001.120.

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