Results 51 to 60 of about 1,687 (159)

Association of aortic and main left coronary aneurysms with severe aortic insufficiency in Takayasu’s arteritis

Clinics and Practice, 2011
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 ...
Marcelo Ferraz de Freitas, Marcelo Valladão de Carvalho, Marcelo Derbli Schafranski   +2 more
doaj   +1 more source

Is prolonged febrile syndrome associated with reactive thrombocytosis a possible association in the diagnosis of Takayasu’s arteritis? A case report

Journal of International Medical Research, 2021
Takayasu’s arteritis is a rare, systemic, inflammatory vasculitis of large blood vessels with an unknown aetiology that more frequently affects women of childbearing age with progression to stenosis, fibrosis or thrombogenesis.
Victoria Birlutiu, Rares-Mircea Birlutiu, Mariana Sandu, Emmanuel Mihali-Oniga   +3 more
doaj   +1 more source

Sequential Balloon Modeling for Robust Percutaneous Transluminal Angioplasty Simulation

International Journal for Numerical Methods in Biomedical Engineering, Volume 42, Issue 7, July 2026.
A sequential balloon modeling (SBM) strategy is proposed to simulate percutaneous balloon angioplasty (PTA) on severe stenosis and estimate post PTA permanent‐set in soft tissues. This strategy promotes simulation robustness. It is combined with a single‐stenosis parametric model and applied to a patient‐case reproduced using the parametric model as ...
Clément Joly, Adrien Kaladji, Aline Bel‐Brunon, Pascal Haigron   +3 more
wiley   +1 more source

Takayasu Arteritis and Giant Cell Arteritis: Results From a Cross‐Sectional Study of 96 Italian Patients

Immunity, Inflammation and Disease, Volume 14, Issue 7, July 2026.
Comparison of epidemiologic, clinical, laboratory, imaging, and treatment response features in 59 patients with Takayasu Arteritis (TAK) and 37 with Giant Cell Arteritis (GCA, 7 C‐GCA, 30 LV‐GCA) at diagnosis and during follow‐up demonstrates that these are distinct diseases, warranting disease‐specific diagnostic and therapeutic approaches.
Marcella Prete, Nicola Susca, Elvira Favoino, Federico Perosa, Daniele Tragni, Luca Navarini, Irene Genovali, Piero Ruscitti, Paola Cipriani, Pasquale Pignataro, Anna Cirulli, Antonio Mazzocca, Patrizia Leone, Vito Racanelli   +13 more
wiley   +1 more source

Application of conventional ultrasound‐based carotid grading system in assessing disease activity and monitoring progression in Takayasu arteritis

Clinical Physiology and Functional Imaging, Volume 46, Issue 4, July 2026.
Abstract Objective This study aimed to evaluate and validate the utility of a conventional ultrasound‐based carotid grading system in assessing disease activity in Takayasu arteritis (TA) with carotid artery involvement, distinguishing between active and inactive patients, and monitoring therapeutic response.
Xuelan Li, Chenyang Zhao, Juan Du, Fengju Liu, Jie Chen   +4 more
wiley   +1 more source

Takayasu’s Arteritis with Systemic Lupus Erythematosus: A Rare Association

Case Reports in Rheumatology, 2015
We report the case of a 24-year-old nondiabetic, nonhypertensive lady with history of fatigue, dyspnoea and limb claudication. She has been diagnosed with Takayasu’s arteritis.
Dhrubajyoti Bandyopadhyay, Vijayan Ganesan, Debarati Bhar, Diptak Bhowmick, Sibnarayan Sasmal, Cankatika Choudhury, Sabyasachi Mukhopadhyay, Adrija Hajra, Manas Layek, Partha Sarathi Karmakar   +9 more
doaj   +1 more source

Atypical Tolosa Hunt syndrome with bilateral sclerokeratitis and optic atrophy in Takayasu's arteritis

American Journal of Ophthalmology Case Reports, 2017
Purpose: We report an interesting case of atypical Tolosa Hunt syndrome with bilateral Sclerokeratitis and optic atrophy in a patient with Takayasu's arteritis.
Kalpana Babu, Deepika C. Parameswarappa
doaj   +1 more source

Australian Guideline for the Identification and Management of Hypertension in Children and Adolescents

Journal of Paediatrics and Child Health, EarlyView.
N. G. Larkins, T. Medley, A. Black, K. A. Bolton, S. Chaturvedi, M. Clark, G. M. Gabb, J. P. Glenning, C. Grimes, R. C. Huang, A. Hyland, C. Jeffries‐Stokes, L. Kalman, S. Kaul, S. Kim, S. McTaggart, R. Kowalski, S. X. Li, S. McNab, D. Metz, A. S. Mihailidou, J. Monin, M. Nelson, M. Pathak, D. Roebuck, M. P. Schlaich, R. Sleaby, C. Quinlan, J. P. Mynard   +28 more
wiley   +1 more source

Performance Characteristics of Anti–Collagen II Antibodies in Relapsing Polychondritis and Related Diseases: Prospective Analysis, Systematic Review, and Meta‐Analysis

Arthritis Care &Research, Volume 78, Issue 6, Page 798-809, June 2026.
Objective Relapsing polychondritis (RP) is a rare disease defined by recurrent cartilaginous inflammation. Anti–collagen II (Col2) antibodies have been proposed as a diagnostic biomarker for RP, but their performance characteristics are not well defined.
Karyssa Stonick, Marcela A. Ferrada, Alice Fike, Kaitlin A. Quinn, Benjamin A. Turturice, Casey Stein, Peter C. Grayson   +6 more
wiley   +1 more source

Catastrophic Antiphospholipid Syndrome in a Young Female Complicated by Systemic Lupus Erythematosus and Left Atrial Myxoma: A Rare Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Catastrophic antiphospholipid syndrome (CAPS) is a fulminant and rare variant of antiphospholipid syndrome characterized by rapidly progressive multiorgan thrombosis and a high mortality rate. Its diagnosis is often challenging due to overlapping clinical features with sepsis, thromboembolic disorders, and systemic autoimmune diseases.
Nazmin Ahmed, Mohammad Nazrul Hossain, Abdullah Salman, Sabrina Yesmin, S. M. G. Saklayen   +4 more
wiley   +1 more source