Behçet's disease overview

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Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Behçet's disease from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
Diagnostic Study of choice
History and Symptoms
Physical Examination
Laboratory Findings
Electrocardiogram
X-Ray
CT
MRI
Echocardiography or Ultrasound
Other Imaging Findings
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2]

Overview

Behçet's disease is a chronic inflammatory condition caused by disturbances in the immune system. The immune system normally protects the body against infections through a controlled inflammatory reaction against the pathogen. In Behçet's disease, the immune response becomes overactive and produces unpredictable outbreaks of exaggerated inflammation. This extra inflammation affects blood vessels, in particular, the smaller vessels. As a result, symptoms appear wherever the exaggerated inflammation response is produced. The inflammatory response can occur anywhere on the body where there is a blood supply.

Historical Perspective

Behcet disease was first discovered by Hippocrates in the 5th century. In 1937, Hulusi Behçet, Turkish dermatologist described Behçet's disease that genital ulcerations, uveitis, and aphthous ulcers are it's major presentations.

Classification

Neurologic disease of Behcet disease is classified into parenchymal or non-parenchymal. Parenchymal disease is due to lesions in the corticospinal tract, brainstem, periventricular white matter, spinal cord, and basal ganglia. Focal parenchymal lesions and complications of vascular thrombosis are the most common abnormalities. Progressive personality change, psychiatric disorders, and dementia may develop. Parenchymal disease may be divided into acuteand chronic progressive neuro-Behçet syndrome. Central nervous system lesions are detectable with MRI. In the chronic phase, lesions may be smaller or resolve, atrophy may be present, nonspecific white matter lesions may be present, and lesions usually do not enhance. Cerebrospinal fluid (CSF) may show increased protein and increased cells, and neutrophils may predominate. Non-parenchymal disease of Behcet disease include cerebral venous thrombosis, intracranial hypertension syndrome (pseudotumor cerebri), acute meningeal syndrome, and uncommonly stroke due to arterial thrombosis, dissection, or aneurysm. On average, a period of approximately five to six years elapsed between the onset of the earliest non-neurologic symptoms of Behçet syndrome and the appearance of neurologic symptoms or findings.

Pathophysiology

It is understood that Behçet disease is the result of vasculitis. It involves all sizes of blood vessels ( small, medium, and large). Arteries and veins are both involved in Behçet disease. Major mechanisms in pathogenesis of Behçet disease include environmental factors such as bacteria, viruses, and heat shock proteins (present in some bacteria and some of the bacterial HSPs share similaritis with human HSPs). Streptococcus sanguinis, streptococcus pyogenes, and mycobacterium tuberculosis produce HSPs that trigger anti HSP60 and anti HSP65 antibodies and then they target human HSPs and immune response such as uveitis in parenchymal neuro-Behçet disease, CD4+ T cells activation, secretion of cytokines and inflammation. Genes involved in the pathogenesis of Behçet disease include human leukocyte antigens, particularly HLA-B51.

Causes

The cause of Behçet disease has not been identified.

Differentiating Behçet's disease from other Diseases

Behçet's disease needs to be differentiated from other diseases that present with similar symptoms such as erythema nodosum and inflammatory bowel disease.

Epidemiology and Demographics

The prevalence of Behçet disease is approximately 0.12 to 7.5 per 100,000 individuals in the United States. Behçet disease commonly affects young adults 20 to 40 years of age. Males are more commonly affected by Behçet disease than females. Behçet disease usually affects individuals of the Turkish, Asian, and Middle Eastern populations. Middle Eastern and Asian individuals are more likely to develop Behçet disease due to the increased incidence of skin pathergy and HLA-B51 antigen. The male to female ratio ranges from approximately 11 to 1 to 2 to 1. The majority of Behçet disease cases are reported along the ancient silk road (from eastern Asia to the Mediterranean).

Risk Factors

Common risk factors in the development of Behcet disease may be occupational, environmental, genetic, and viral. Behçet's disease can affect people in any age, but the most common age is 20~30 years old. Behçet's disease is more common in Middle East and Japan then in other race. It is rare in America. Researches demonstrate that the presence of the gene HLA–B51 is a risk factor for Behçet's disease.

Screening

There is insufficient evidence to recommend routine screening for Behçet disease.

Natural History, Complications and Prognosis

The symptoms of Behçet disease usually develop in the second to third decade of life, and start with symptoms such as uveitis, mouth sores, and skin lesions. Common complications of Behçet disease include neuro Behçet, vision loss, and aneurysm. Depending on the extent of the disease at the time of diagnosis, the prognosis may vary. However, the prognosis is generally regarded as good. The worst prognoses are associated with retinal vasculitis, leading to blindness; vascular aneurysm formation, with possible rupture; and neuro–Behçet syndrome, which may lead to dementia despite appropriate aggressive treatment.

Diagnosis

Diagnostic Study of Choice

Currently, there is not a specific test to confirm the diagnosis of Behçet's disease. It is diagnosed clinically by specific patterns of symptoms and repeated outbreaks obtained by a thorough history of the patient's symptoms (outlined below). Behçet's disease is a diagnosis of exclusion, and other chronic inflammatory diseases should be evaluated for. The various inflammatory symptoms do not necessarily occur together, and they will vary in severity.

History and Symptoms

The hallmark of Behçet disease is recurrent aphthous ulcerations, genital ulcers, and uveitis. A positive history of joint pains and skin lesions are suggestive of Behçet disease. The most common symptoms of Behçet disease include mouth sores, uveitis, joint pain, and genital sores. Less common symptoms of Behçet disease include diarrhea, abdominal pain, headache, skin lesions-red nodules, acne, joint pains, and poor balance.

Physical Examination

Patients with Behçet disease usually appear normal. Vital signs of patients with Behçet disease are usually normal. The presence of mouth sores, genital ulcers, and vision problems on physical examination are diagnostic of Behçet disease. Skin examination of patients with Behçet disease shows erythema nodosum lesions typically occur on the extremities, especially the lower legs, but they can also be observed on the face, neck, and buttocks. The lesions are painful and resolve spontaneously, although some may ulcerate or leave hyperpigmentation. A folliculitis like rash, resembling acne vulgaris, appears on the face, neck, chest, back, and hairline of patients. Some lesions become more pustular; 24-48 hours after a sterile needle prick, some patients develop erythema with a nodule or pustule at the prick site. Ophthalmoscopic exam may be abnormal with findings of retinal vasculitis, and vaso-occlusive lesions. Uveitis of anterior and posterior chambers diagnosed with slit-lamp examination. Erythematous throat with tonsillar swelling, and exudates. Ulcers 2-15 mm in diameter, with a necrotic center and surrounding red rim. A white or yellow pseudomembrane covers the surface of the ulcer. The ulcers are typically painful, nonscarring, and found on the lips, buccal mucosa, tongue, tonsils, and larynx. Most last 7-14 days and occur in crops. Hypopyon may be observed in the anterior chamber. Genitourinary examination of patients with Behçet disease will show ulcers on the scrotum and vulva, painful and heal with scarring. Genital ulcerations tend to be deeper and larger than the oral lesions. Females can have asymptomatic ulcers. Neuromuscular examination of patients with Behçet disease will show CNS involvement in 25% of the cases. Immune-mediated meningoencephalitis predominantly involves the brainstem. Meningitis, encephalitis, focal neurological deficits, and psychiatric symptoms can be present. Irreversible dementia can occur.

Laboratory Findings

The laboratory tests used to diagnose Behçet's disease are a pathergy test, a skin biopsy, and a lumbar puncture.

Electrocardiogram

There are no ECG findings associated with Behçet's disease.

X-ray

There are no x-ray findings associated with Behçet disease.

Echocardiography and Ultrasound

Echocardiography is useful in patients with murmurs because it is useful for diagnosing the valve vegetations and ventricular thrombi, which may occur in Behçet disease. Vascular involvement can be seen in up to 40% of patients with Behçet disease (BS) with the lower-extremity vein thrombosis (LEVT) being the most common type where ultrasonography is needed.

CT Scan

There are no CT scan findings associated with Behçet disease. However, a CT scan may be helpful in the diagnosis of complications of Behçet disease including visualization of neurological lesions (helpful in patients with CNSinvolvement), and enlargement of ventricles or subarachnoid spaces.

MRI

There are no MRI findings associated with Behçet disease. MRI findings of the brain may be normal even in the presence of neurologic involvement. However, a MRI may be helpful in the diagnosis of complications of Behçet disease, which include enlargement of ventricles or subarachnoid spaces, and neurological lesions present in CNS involvement.

Other Imaging Findings

Endoscopy of the GI tract is useful for detecting gastrointestinal ulcerations in Behçet disease. A thorough eye examination and fluorescein angiography for evaluation of retinal vessels. Follow-up visits with an ophthalmologist should be scheduled at least every 6-12 months. Neuropsychologic testing may be useful with CNS involvement, revealing memory impairment or personality changes, and can be useful in monitoring neuropsychologic status.

Other Diagnostic Studies

There are no other diagnostic studies associated with Behçet disease.

Treatment

Medical Therapy

Current treatment is aimed at easing the symptoms, reducing inflammation, and controlling the immune system. Anti-TNF therapy, such as infliximab, has shown promise in treating the uveitis associated with the disease. Another Anti-TNF agent, etanercept, may be useful in patients with mainly skin and mucosal symptoms. Interferon alfa-2a, azathioprine, colchicine, thalidomide, dapsone and rebamipide are among other agents that are used alternatives.

Surgery

Surgery in Behcet's disease is performed to treat severe complications such as gastrointestinal perforations or ocular inflammatory diseases.

Primary Prevention

There are no established measures for the primary prevention of Behçet disease.

Secondary Prevention

There are no established measures for the secondary prevention of Behçet disease.