Results 11 to 20 of about 12,922 (226)

Coexistence of Takayasu Arteritis and Intestinal Tuberculosis in a Young Bangladeshi Woman. [PDF]

Clin Case Rep
ABSTRACT Takayasu arteritis (TAK) is a rare, chronic, granulomatous large‐vessel vasculitis predominantly affecting young women. Although its etiology remains uncertain, tuberculosis (TB) has long been implicated as a potential trigger. We report a 28‐year‐old Bangladeshi woman with TAK coexisting with transverse colon TB, a rare but clinically ...
Debnath S, Ahmed QMU, Mahbub S, Khan I, Uddin MA, Rahman SME.   +5 more
europepmc   +2 more sources

Outcomes of an Intravenous to Subcutaneous Infliximab (CT-P13) Strategy in Takayasu Arteritis: A Proof-of-Concept Prospective Study. [PDF]

ACR Open Rheumatol
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 ...
Iorio L, Davanzo F, Fiorin E, Codirenzi M, Prevedello R, Doria A, Padoan R.   +6 more
europepmc   +2 more sources

Immunoglobulin G4-Related Disease-Like Gastric Lesion Presenting as Submucosal Tumor-Like Lesions. [PDF]

DEN Open
ABSTRACT Immunoglobulin G4 (IgG4)‐related disease (RD) is a systemic fibroinflammatory condition characterized by infiltration of IgG4‐positive plasma cells (PCs). Gastrointestinal involvement may present as submucosal tumor–like lesions and poses diagnostic challenges.
Kuroda T, Miyaguchi K, Tsuzuki Y, Yamaguchi H, Imaeda H.   +4 more
europepmc   +2 more sources

Takayasu Arteritis [PDF]

Frontiers in Pediatrics, 2018
La arteritis de Takayasu es una vasculitis granulomatosa idiopática de la aorta y sus ramas principales. Es más frecuente entre los asiáticos y las mujeres, y constituye una de las vasculitis más comunes en los niños. La inflamación y la proliferación de la íntima conducen al engrosamiento de la pared, lesiones estenóticas u oclusivas y trombosis ...
Ricardo Russo, María M. Katsicas
openaire   +3 more sources

Takayasu's arteritis [PDF]

The Journal of the American Osteopathic Association, 1989
Takayasu's arteritis, an inflammatory and obliterative disease of medium and large arteries, is classified as a giant cell arteritis. It has a predilection for the aortic arch and its branches and the pulmonary arteries. Unlike atherosclerotic vascular diseases, Takayasu's arteritis affects young women primarily.
openaire   +2 more sources

Takayasu arteritis

Scandinavian Journal of Rheumatology, 2005
Introduction. Giovanni Battista Morgani reported the first case with Takayasu arteritis (TA) in 1761. The disease affects the aortic arch and large blood vessels. It is found in every race and in every age-group, predominantly in female population aged 20-40 years.
Sidor, Misović, Miroljub, Drasković, Miodrag, Jevtić, Momir, Sarac   +3 more
openaire   +5 more sources

Takayasu arteritis in pregnancy: A case series [PDF]

Perspectives In Medical Research, 2020
Takayasu arteritis is a disease of unknown etiology which is a primary systemic vasculitis leading to stenotic and occlusive changes. Takayasu arteritis is a chronic inflammatory disease in progressive pattern which chiefly affects the aorta and its ...
Ipsita Mohapatra1 , Subha Ranjan Samantaray1 ,G Priyanka2 , Achanta Vivekananda1
doaj   +1 more source

Concurrent coronary artery and subclavian arterial aneurysms in Takayasu arteritis

The Egyptian Journal of Radiology and Nuclear Medicine, 2021
Background Aneurysmal coronary artery involvement and subclavian artery aneurysm are extremely uncommon in Takayasu arteritis. Case presentation We present a case with concurrent coronary artery and subclavian artery aneurysms.
Anoop Ayyappan, Arun Gopalakrishnan, Shivanesan Pitchai   +2 more
doaj   +1 more source

The angiographic and clinical profile of patients with Takayasu aortoarteritis

Heart Vessels and Transplantation, 2023
Objective: Takayasu arteritis is a rare, chronic, inflammatory disease that primarily affects the aorta and its major branches. It mainly affects young females, and it can cause significant morbidity and mortality if untreated.
Jitendra Sharma, Tarun Madan, Dinesh Joshib, Riyaz Charaniya, Pratik Raval, Vishal Sharma, Himani Upadhyaya, Krutika Patel   +7 more
doaj   +1 more source

Spectrum of imaging findings in Takayasu arteritis—A case report

Radiology Case Reports, 2022
Takayasu arteritis (TA) is an uncommon chronic granulomatous inflammatory disease often affecting the aorta and its branches. Early diagnosis is quite challenging due to nonspecific symptoms and unfamiliarity with the disease. We hereby present a case of
Kritisha Rajlawot, MD, Sujan Thapa, MD, Asim Sitaula, MD, Nirmal Prasad Neupane, MD   +3 more
doaj   +1 more source