Results 61 to 70 of about 41,602 (220)

Outcomes of an Intravenous to Subcutaneous Infliximab (CT‐P13) Strategy in Takayasu Arteritis: A Proof‐of‐Concept Prospective Study

ACR Open Rheumatology, Volume 8, Issue 1, January 2026.
Objectives To evaluate persistence, outcomes, safety, and remission maintenance after switching from intravenous infliximab (IV‐IFX) to subcutaneous infliximab (SC‐IFX, CT‐P13) in patients with Takayasu arteritis (TA). Methods We conducted a prospective, single‐center, proof‐of‐concept observational study of consecutive adults with TA in sustained ...
Luca Iorio, Federica Davanzo, Eleonora Fiorin, Marta Codirenzi, Roberta Prevedello, Andrea Doria, Roberto Padoan   +6 more
wiley   +1 more source

Consensus Statement on Precision Anatomy and Treatment Strategies for Median Arcuate Ligament Syndrome: AOB Consensus Meeting

Asian Journal of Endoscopic Surgery, Volume 19, Issue 1, January/December 2026.
ABSTRACT Background With the increasing use of minimally invasive surgery, understanding of the precise anatomy involved in median arcuate ligament syndrome (MALS) has advanced. However, surgical strategies and treatment principles for MALS remain unclear.
Hidenori Haruta, Masaharu Higashida, Katsuyuki Hoshina, Toshio Takayama, Tomotaka Ueno, Saya Chiba, Noboru Ideno, Naoki Ikenaga, Shunji Endo, Yasunaru Sakuma, Toshiya Abe, Kenoki Ouchida, Masafumi Nakamura, Yuko Kitagawa, Akiko Umezawa   +14 more
wiley   +1 more source

Noninfectious Necrotizing Aortitis With Predominantly Neutrophilic Infiltrate

Case Reports in Pathology, Volume 2026, Issue 1, 2026.
Aortitis can be either infectious or noninfectious, and cases of noninfectious aortitis are not well understood. Our study presents a case of noninfectious ascending aortitis in a relatively young, previously healthy man, characterized by a predominantly neutrophilic infiltrate on histopathological examination without an inciting microorganism.
Nathan A. Williams, Mark Colantonio, Anastasia Miller, Allen P. Burke, Suraiya Saleem   +4 more
wiley   +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

A Rare Case of Giant Cell Arteritis Affecting Two Giants: Pulmonary and Root of Aorta Aneurysm

Clinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Aneurysms of pulmonary arteries and aorta are rare, typically caused by infections, congenital heart defects, vascular abnormalities, or medical interventions. This report presents an unusual case of a 72‐year‐old man with a history of smoking, hypertension, and emphysema, who was found to have a large pulmonary artery aneurysm (63.5 mm) and ...
Gajendra Acharya, Hafiza Baloch, Pradeep Masuta, Rohit Pandit, Robert Kimelheim, Prabal Tiwari   +5 more
wiley   +1 more source

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

A Case of Isolated Aortic Regurgitation, Later Diagnosed as Takayasu Arteritis: An Importance of Physical Examinations

Clinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Takayasu arteritis is a large vessel vasculitis involving the aorta and its branches. It has a wide spectrum of clinical manifestations and lacks specific diagnostic markers. Here we present a case of a 30‐year‐old female with isolated aortic regurgitation who presented with constitutional symptoms.
Tshering Penjor, Thinley Dorji, Sangay Wangchuk, Thai Wangmo, Sonam Yangzom, Sonam Wangchuk   +5 more
wiley   +1 more source

Takayasu Arteritis in a 55‐Year‐Old Woman With Prior Mycobacterium leprae Infection: A Possible Postinfectious Association

Clinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Takayasu arteritis (TAK) is a rare large‐vessel vasculitis affecting the aorta and its major branches. Although autoimmune mechanisms are central, prior mycobacterial infections have been hypothesized to contribute to the disease onset. A 55‐year‐old South Asian woman with a history of vitiligo and treated multibacillary leprosy presented with
Ujjawal Bhattarai, Abhisek Jha, Ishan Shrestha, Naphibanroi Lamar, Mandakini Parajuli, Sanjay Bhujel, Dipen Majhi, Kritika Paudel   +7 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

Prevalence of vasculitis, systemic lupus erythematosus, rheumatoid arthritis, systemic sclerosis, idiopathic inflammatory myopathies and spondyloarthritis in Australia: a systematic review and meta‐analysis

Internal Medicine Journal, Volume 55, Issue 12, Page 1985-1996, December 2025.
ABSTRACT Background Systemic autoimmune rheumatic diseases (SARDs), including vasculitis, systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), systemic sclerosis (SSc), idiopathic inflammatory myopathies (IIM), spondyloarthritis (SpA), Sjogrens disease (SjD) and mixed connective tissue disease (MCTD), are rare but associated with substantial ...
L. Roper, E. Cameron, T. Yu, N. Li, M. Parker, N. Nassar, M. Nikpour   +6 more
wiley   +1 more source