MALADIE DE BEHCET. MALADIES AUTO-‐INFLAMMATOIRES. G. KAPLANSKI. Service de Médecine Interne, CH Concep`on,. Marseille. INSERM UMR_S Behçet’s disease: from Hippocrates to the Third Millenium. Br J Ophthalmol ; 3 Wechsler B, Du-Boutin LTH, Amoura Z. Maladie de Behçet. La maladie de Behçet autochtone. À propos de 73 cas. Rev Rhum 4. Yurdakul S., et al. The prevalence of Behçet’s syndrome in a rural area.
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Report of a case with pericardial effusion and cryoglobulinemia treated with indomethacin. Current treatment is aimed at easing the symptoms, reducing inflammation, and controlling the immune system.
Surgical treatment of arterial manifestations of BD bears many pitfalls, since the obliterative endarteritis of vasa vasorum causes thickening of the medial layer and splitting of elastin fibers.
Superficial and deep lower limb thrombosis is the most frequent venous complications but one third of venous thrombosis concern large vessels such as cerebral venous thrombosis, pulmonary embolism, and inferior or superior vena cava, etc. Despite the inclusive criteria set forth by the International Study Group, there are cases where not all the criteria can be met and therefore a diagnosis cannot readily be made.
Br Heart J Palate Bednar’s aphthae Cleft palate High-arched palate Palatal cysts of the newborn Inflammatory papillary hyperplasia Stomatitis nicotina Torus palatinus.
Maladie de Behçet de l’enfant – EM|consulte
A report of 11 cases studied by optic, ultrastructural and immunopathological technics. Am J Gastroenterol In the UK, it is estimated to have about 1 case for everypeople. Br J Rheumatol Ocular involvement can be in the form of posterior uveitisanterior uveitisor retinal vasculitis. Top of the page – Article Outline.
Diagnosis is based on clinical manifestations since there are no pathognomonic laboratory findings. Interferon alpha-2a may also be an effective alternative treatment, particularly for the genital and oral ulcers  as well as ocular lesions.
Other Eagle syndrome Hemifacial hypertrophy Facial hemiatrophy Oral manifestations of systemic disease. Progressive optic atrophy may result in decreased visual acuity or color vision.
J Am Coll Surg Annales d’oculistique, Paris, Treatment is based on corticosteroids and immunosuppressive drugs. However, cases of acute optic neuropathy specifically anterior ischemic optic neuropathy have also been reported to occur.
Colchicine myopathy and neuropathy.
J Roy Soc Med The cause is not well-defined, but it is primarily characterized by auto-inflammation of the blood vessels. Periapical, mandibular and maxillary hard tissues — Bones of jaws. Retrieved 29 May Archived from the original on 29 July Orofacial soft tissues — Soft tissues around the mouth Actinomycosis Angioedema Basal cell carcinoma Cutaneous sinus of dental origin Cystic ce Gnathophyma Ludwig’s angina Macrostomia Melkersson—Rosenthal syndrome Microstomia Noma Oral Crohn’s disease Orofacial granulomatosis Perioral dermatitis Pyostomatitis vegetans.
Basal cell adenoma Canalicular adenoma Ductal papilloma Monomorphic adenoma Myoepithelioma Oncocytoma Papillary cystadenoma lymphomatosum Pleomorphic adenoma Sebaceous adenoma Malignant: Archived from the original on 27 January Cluzel cG. Rev Mal Resp 2: Intracranial hypertension with papilledema may be present. A large number of serological studies show a linkage between the bebet and HLA-B J Am Acad Dermatol Retrieved 19 September Therefore, anastomotic pseudoaneurysms are likely to form, as well as pseudoaneurysms at the site of puncture in case of angiography or endovascular treatment; furthermore, early graft occlusion may occur.
IVIG could be a treatment for severe  or complicated cases.
John Libbey Eurotext – Médecine thérapeutique – Maladie de Behçet
Access to the full text of this article requires a subscription. Archived from the original on 10 July Eur Heart J 7: A study in 25 patients. Cardiovasc Intervent Radiol 9: Cardiovasc Intervent Radiol Am J Surg Pathol 5: