Behcet disease: advantageous against development of neoplasia?
نویسندگان
چکیده
منابع مشابه
[Behcet disease].
Central nervous system involvement in Behçet disease (BD) may be either parenchymal or nonparenchymal. Abnormal cerebrospinal fluid findings and parenchymal involvement are associated with a poorer prognosis. A self-antigenic role for HLA B51 has been postulated in the pathogenesis of BD. The sibling occurrence rate is 3.6%. Familial aggregation may be more pronounced among pediatric cases comp...
متن کاملImmunology of Behcet disease: review article
Behçet's disease (BD), also known as the Silk Road disease, is a multisystemic and rare inflammatory disorder primarily prevalent in populations along the Mediterranean Sea. Today, BD is defined as a crossroad between autoimmune and auto-inflammatory syndromes. Variety of syndromes including mucocutaneous manifestations such as oral and genital ulcers, papulopustular lesions and erythema nodosu...
متن کاملNeurological Manifestations in Behcet Disease
Behçet disease is a multisystem disease of unknown cause in which an inflammatory perivasculitis can arise in almost any tissue (Sakane et al., 1999). Neurologic involvement in Behçet disease was first reported by Knapp in 1941. It represented between 4-49% of manifestations of BD (Haghighi et al., 2005). There is one of the most serious causes of long term morbidity and mortality in Behçet’s D...
متن کاملOcular expressions of children behcet disease
Results Our patients were 4 to 15 years old ( average 10,78 years ). Ocular signs were found at 13 cases among 19 followed for behcet disease ( 68,4% ). The attack was bilateral in 11 cases ( 84% ). In 2 cases, ocular attack was inaugural. The uveitis was total in 3 patients, anterior in 3 others cases, intermediar in 2 cases, severe in one case. Papillar oedema was noted in 2 cases, retinian v...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Annals of the Rheumatic Diseases
سال: 1996
ISSN: 0003-4967
DOI: 10.1136/ard.55.9.648-a