Arterial and venous involvement in Behçet's syndrome: a narrative review

N Toledo-Samaniego, CM Oblitas… - Journal of Thrombosis …, 2022 - Springer
Behçet syndrome (BS) is a unique type of vasculitis that affects veins and arteries of all
sizes, leading to recurrent vascular events, mostly venous thrombosis. The prevalence of …

Positron emission tomography imaging in vasculitis

KSM van der Geest, BGC Slijkhuis… - Cardiology …, 2023 - cardiology.theclinics.com
Systemic vasculitides are autoimmune diseases characterized by inflammation of blood
vessels. Their categorization is based on the size of the preferentially affected blood vessels …

Imaging manifestations of Behcet's disease: key considerations and major features

G Mehdipoor, F Davatchi, H Ghoreishian… - European journal of …, 2018 - Elsevier
Behcet's disease is an autoimmune disease most commonly seen in the Middle East.
Although primarily known with painful oral and genital ulcers, it can lead to vasculitis …

Intracardiac thrombus in patients with Behcet's disease: clinical correlates, imaging features, and outcome: a retrospective, single-center experience

H Wang, X Guo, Z Tian, Y Liu, Q Wang, M Li… - Clinical …, 2016 - Springer
Intracardiac thrombus (ICT) is a rare but serious complication of Behcet's disease (BD). The
study was to report the clinical characteristics, imaging features, treatment, and outcomes of …

Cardiovascular disease in the systemic vasculitides

S Soulaidopoulos, AV Madenidou… - Current Vascular …, 2020 - ingentaconnect.com
The vasculitides are a heterogeneous group of disorders, characterized by inflammatory cell
infiltration and necrosis of blood vessels that cause vascular obstruction or aneurysm …

[PDF][PDF] Intracardiac thrombus in Behçet's disease

IB Ghorbel, N Belfeki, MH Houman - Reumatismo, 2016 - reumatismo.org
Behçet's disease (BD) is a multisystem inflammatory disorder. Intracardiac thrombus (ICT)
formation is an uncommon but important complication of BD. Of the cases of Behçet's …

[HTML][HTML] Enigmatic odyssey: A case of Behcet disease with atypical thrombotic complications

HA Abdul-Hafez, Y Hamdan, NAA Hamdeh… - International Journal of …, 2024 - Elsevier
Introduction and importance Behçet disease is a rare, chronic, multi-systemic inflammatory
disease of unknown origin that affects vessels in various organs. It is characterized by …

Cardiac involvement in the adult primary vasculitides

G Pazzola, N Pipitone, C Salvarani - Expert Review of Clinical …, 2020 - Taylor & Francis
Introduction Heart involvement in vasculitis is rare, but potentially severe. The ascertainment
of cardiac disease in vasculitis is complex and requires an integrated multidisciplinary …

Intracardiac thrombosis in Behçet's Disease successfully treated with immunosuppressive agents: A case of vascular pathergy phenomenon

F Galeano-Valle, P Demelo-Rodriguez… - Intractable & Rare …, 2018 - jstage.jst.go.jp
Behçet's Disease (BD) is a rare multi-systemic inflammatory disorder classified as a systemic
vasculitis of unknown aetiology. Vascular involvement occurs in approximately 5-51.6 …

An adolescent case of extensive Behcet's disease successfully treated with Infliximab

E Isiyel, S Bakkaloglu, A Oguz, İ Yenicesu… - Turkish Journal of …, 2019 - avesis.gazi.edu.tr
Cardiac involvement is an uncommon and life-threatening complication of Behget's Disease.
We present a 14-year-old boy, admitted to our hospital for recurrent hemoptysis. In his …