Behcet's

From WikiMD's Food, Medicine & Wellness Encyclopedia


Behçet's disease, also known as Behçet's syndrome or Silk Road disease, is a rare, chronic, autoimmune disease that causes blood vessel inflammation throughout the body. The disease is named after Hulusi Behçet, a Turkish dermatologist who first described the condition in 1937.

Symptoms[edit | edit source]

The symptoms of Behçet's disease can vary widely among individuals but commonly include:

Other symptoms may include arthritis, gastrointestinal issues, and neurological problems.

Complications[edit | edit source]

Complications of Behçet's disease can be severe and may include:

Causes[edit | edit source]

The exact cause of Behçet's disease is unknown. It is believed to be a combination of genetic predisposition and environmental factors. Certain genes, such as HLA-B51, have been associated with an increased risk of developing the disease.

Diagnosis[edit | edit source]

Diagnosis is primarily based on clinical criteria, which include recurrent oral ulcers along with at least two other symptoms such as genital ulcers, eye inflammation, or skin lesions. The pathergy test, where a small needle prick leads to a skin reaction, can also aid in diagnosis.

Differential Diagnosis[edit | edit source]

Conditions that may present similarly to Behçet's disease include:

Treatment[edit | edit source]

There is no cure for Behçet's disease, but treatment aims to reduce symptoms and prevent complications. Common treatments include:

Prognosis[edit | edit source]

The prognosis for Behçet's disease varies. Some individuals may experience mild symptoms, while others may have severe complications. Early diagnosis and treatment are crucial for managing the disease effectively.

Related Pages[edit | edit source]

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Contributors: Prab R. Tumpati, MD