نتایج جستجو برای: vascular diseases hypertension headache takayasu arteritis bell palsy

تعداد نتایج: 1174461  

2011
Mohammad G Ishaq Fahad A Shabbir

INTRODUCTION The simultaneous presence of Takayasu's arteritis and beta thalassemia trait is a rare combination. To the best of our knowledge, this is the first case report on Takayasu's arteritis and beta thalassemia presenting together. CASE PRESENTATION This is a case report of a 23-year-old Asian woman of Pakistani descent who presented with a headache, blurred vision and dizziness. CON...

Journal: :European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery 2014
Sven C Steireif Gregor J Kocher Florin T F Gebhart Ralph A Schmid

Pulmonary artery aneurysm in adults is a rare diagnosis. Most cases described in the literature are either associated with congenital heart disease or pulmonal arterial hypertension, respectively, or are not true aneurysms but rather pseudoaneurysms, which are usually iatrogenic. We present the case of a 68-year old female patient with the incidental finding of a true aneurysm of the right peri...

Journal: :Annals of the Rheumatic Diseases 2023

Background Revascularization endovascular techniques have been used with success in Takayasu arteritis (TA), but relapses sometimes appear. (1) There is much debate regarding optimal management and outcomes of patients who underwent these procedures. (2,3) Objectives The aim the study was to investigate long-term efficacy percutaneous transluminal angioplasty (PTA) TA from a Romanian tertiary r...

Journal: :Circulation 2008
Hitoshi Ogino Hitoshi Matsuda Kenji Minatoya Hiroaki Sasaki Hiroshi Tanaka Yu Matsumura Hatsue Ishibashi-Ueda Junjiro Kobayashi Toshikatsu Yagihara Soichiro Kitamura

Takayasu arteritis (TA), which is a nonspecific inflammatory disease of unknown origin, causes various types of aortoarterial stenosis/occlusion or dilatation (Figure). Historically, Mikito Takayasu, a Japanese ophthalmologist, described a peculiar wreathlike arteriovenous anastomosis around the papillae of the retina (Takayasu disease) in 1908.1 In the first necropsy case reported in 1940, thi...

Journal: :The Journal of rheumatology 2014
Enrico Tombetti Maria Chiara DI Chio Silvia Sartorelli Andrea Segalini Yole Vella Matteo Spalluto Maria Grazia Sabbadini Elena Baldissera Angelo Manfredi

Journal: :Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir 2014
Taner Şeker Ahmet Oytun Baykan Abdurrezzak Börekçi Mustafa Gür Murat Çaylı

We report a case of thrombus treated with thrombolytic therapy in a patient with normal cardiac functions and Takayasu arteritis. A 27-year-old man with a history of Takayasu arteritis was admitted to our out-patient clinic with a complaint of both right and left foot pain and weakness. In a Doppler ultrasound examination, a subtotal thrombotic occlusion was found in the bilateral popliteal art...

2004
Mikito Takayasu Manotosh Panja Prakas Chandra Mondal

191 Takayasu’s Arteritis (TA) is an inflammatory vascular disease involving the aorta and its major branches as well as the pulmonary artery and its branches1.It was introduced to the medical fraternity in 1827 by Dr. R. Adams2 who was the first physician to note absence of pulse in all four extremities. In 1856 Savory3 reported a case of young female with absence of pulses. In 1908, Dr. Mikito...

2016
Enrico Tombetti Barbara Colombo Maria Chiara Di Chio Silvia Sartorelli Maurizio Papa Annalaura Salerno Enrica Paola Bozzolo Elisabetta Tombolini Giulia Benedetti Claudia Godi Chiara Lanzani Patrizia Rovere-Querini Alessandro Del Maschio Alessandro Ambrosi Francesco De Cobelli Maria Grazia Sabbadini Elena Baldissera Angelo Corti Angelo A Manfredi

BACKGROUND Chromogranin-A (CgA) is a secretory protein processed into peptides that regulate angiogenesis and vascular cells activation, migration and proliferation. These processes may influence arterial inflammation and remodelling in Takayasu arteritis (TA). METHODS Plasma levels of full-length CgA (CgA439), CgA fragments lacking the C-terminal region (CgA-FRs) and the N-terminal fragment,...

2014
Nienke de Graeff Noortje Groot Sylvia Kamphuis Pavla Dolezalova Despina Eleftheriou Annet van Royen Marinka Twilt Seza Ozen Paul Brogan Michael Beresford

Introduction Polyarteritis Nodosa (PAN), Granulomatosis with Polyangiitis (GPA), Microscopic Polyangiitis (MPA), Eosinophilic Granulomatosis with Polyangiitis (EGPA) and Takayasu Arteritis (TA) are rare paediatric vasculitides that can lead to significant morbidity. Evidence-based guidelines are sparse and management is mostly based on physician experience. Consequently, treatment regimens diff...

Journal: :Arthritis and rheumatism 2007
Philip Seo John H Stone

Introduction The vasculitides include a broad spectrum of disorders that span a clinical spectrum from benign, self-limited disease to fulminant conditions that are fatal in the absence of therapy. Whereas the large-vessel vasculitides consist of 2 principal disorders, giant cell arteritis and Takayasu arteritis, the mediumand small-vessel vasculitides are much more diverse, including multiple ...

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