Gotowe bibliografie tematyczne / Takayasu’s arteritis in women

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  4. Części książek
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Gotowa bibliografia na temat „Takayasu’s arteritis in women”

Autor: Grafiati
Data publikacji: 2 czerwca 2025
Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Takayasu’s arteritis in women"

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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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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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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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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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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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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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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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Dogra, Amisha, and Uma N. Wankhede. "Takayasu’s arteritis in pregnancy: a rare case report from BJGMC and Sassoon Hospital Pune, Maharashtra, India." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 6, no. 8 (2017): 3703. http://dx.doi.org/10.18203/2320-1770.ijrcog20173519.

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Takayasu’s arteritis is a chronic idiopathic vasculitis affecting aorta and its primary branches, commonly seen in young women of Asian or oriental descent during child bearing age. Incidence is 2.6 cases/million/year. It affects females in the reproductive years accounting for almost 80% of the cases. A 34 year female G2P1L1 with 9 months of amenorrhea with previous LSCS known case of takayasu arteritis, epilepsy with right side hemiparesis with aphasia. She proceeded to have elective LSCS with ventouse delivery under epidural anaesthesia and delivered alive healthy female baby weight 2.4 kg
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Kaur, Sukhdeep, Avneet Kaur, Aditi Sehajpal, and Seema Rai. "Takayasu’s arteritis: a diagnostic dilemma." International Journal of Research in Medical Sciences 13, no. 5 (2025): 2192–95. https://doi.org/10.18203/2320-6012.ijrms20251335.

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Takayasu`s arteritis is an uncommon form of chronic vasculitis that primarily affects medium and large blood vessels, including the aorta and its major branches. The disease is mainly seen in young women. This is marked by mononuclear cell infiltration and granulomatous inflammation within the vascular media. These pathological changes result in thickening of the arterial wall, which can lead to stenosis, occlusion, or the formation of aneurysms. It can lead to severe complications such as stroke, ischaemic heart disease, pulmonary hypertension, secondary hypertension and aneurysm formation. H
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Punukula, Harichandana, Bospali Kavya Sree, Vaka Pratyusha, and Swetha Bospaly. "A CASE REPORT ON TAKAYASU ARTERITIS." International Journal of Advanced Research 8, no. 9 (2020): 1289–93. http://dx.doi.org/10.21474/ijar01/11787.

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Takayasus arteritis primarily affects young women. Takayasu arteritis (TA) is a type of primary systemic vasculitis mainly affecting the medium and large arteries. The signs and symptoms are due to systemic inflammation or ischemia of an organ or limb and include angiodynia, claudication, peripheral pulselessness, murmurs, ischemic stroke, myocardial infarction and severe systemic arterial hypertension. The disease tends to affect more women than men.The current case of Takayasu arteritis type V focuses on a 21 year female who complained of cold, cough, fever, facial puffiness since 2 months,
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Rozprawy doktorskie na temat "Takayasu’s arteritis in women"

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Samartinho, Marta Maria Duarte. "Prevalence of stroke and transient ischemic attack in Takayasu’s arteritis : a systematic review." Master's thesis, 2015. http://hdl.handle.net/10451/25920.

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Trabalho Final do Curso de Mestrado Integrado em Medicina, Faculdade de Medicina, Universidade de Lisboa, 2015<br>Background: Takayasu's Arteritis (TA) is a systemic panarteritis affecting primarily large arteries. Cerebrovascular disease is one of the possible manifestations of TA, adding to disease burden. Objectives: To systematically review the prevalence of stroke/TIA in TA patients, as well as its epidemiological and clinical features. Methods: References were researched in MEDLINE and EMBASE databases and from searching the references of original articles and reviews. Abstracts and titl
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Książki na temat "Takayasu’s arteritis in women"

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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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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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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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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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Rupp, James. Giant Cell Arteritis - an Elusive Odyssey. Lulu Press, Inc., 2008.

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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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Części książek na temat "Takayasu’s arteritis in women"

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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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Streszczenia konferencji na temat "Takayasu’s arteritis in women"

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Cavalli, G., A. Tomelleri, E. Baldissera, and L. Dagna. "FRI0325 Prevalence of takayasu arteritis in young women with acute ischemic heart disease." In Annual European Congress of Rheumatology, 14–17 June, 2017. BMJ Publishing Group Ltd and European League Against Rheumatism, 2017. http://dx.doi.org/10.1136/annrheumdis-2017-eular.2298.

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Moreira Lima Rebouças, Lidiane, Alexandra de Oliveira Lopes, Samara Belchior Gaído, et al. "CASE REPORT: ISCHEMIC STROKES AND KINKINGS OF INTERNAL CAROTID ARTERIES IN YOUNG WOMEN. ANTIPHOSPHOLIPID SYNDROME OR TAKAYASU ARTERITIS?" In Congresso Brasileiro de Reumatologia 2020. Sociedade Brasileira de Reumatologia, 2021. http://dx.doi.org/10.47660/cbr.2020.17011.

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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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