Behçet syndrome is a rare, chronic inflammatory disease of unknown aetiopathogenesis,
most commonly presenting with mucocutaneous and ocular manifestations. Vascular …

Objective To assess the efficacy and safety of treatment modalities for major organ
involvement of Behçet's syndrome (BS), in order to inform the update of the EULAR …

Behcet's syndrome (BS) is a variable vessel vasculitis with heterogeneous clinical features.
Skin, mucosa and joint involvement can cause impairment of quality of life but do not cause …

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 …

Behçet's syndrome (BS) is a multisystem vasculitis that presents with a variety of
mucocutaneous manifestations such as oral and genital ulcers, papulopustular lesions and …

Cardiac involvement is common in primary systemic vasculitides and may be due to direct
effect of the disease on the heart or due to therapy. We shall review involvement of the heart …

Systemic autoimmune diseases can affect various kinds of organs including the kidney, the
skin, soft tissue and the bone. Among others, cardiovascular involvement in rheumatic …

Behçet syndrome is considered to be a multisystemic vasculitis involving the skin, mucosa,
eyes, joints, nervous system, cardiovascular system, and gastrointestinal system. The exact …

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 …

Autoimmune diseases are not infrequently associated with arterial or venous thrombotic
events. Chronic inflammation and immune system impairment are considered the main …