ARTIGO ORIGINAL. Acometimento pulmonar na doença de Behçet: uma boa experiência com o uso de imunossupressores. Alfredo Nicodemos Cruz Santana I;. Behçet disease is characterized by a triple-symptom complex of at a lower threshold than in individuals who do not have Behçet disease. Download Citation on ResearchGate | On Dec 31, , D.M.N. Filho and others published ACOMETIMENTO INTESTINAL DA DOENÇA DE.

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By using this site, you agree to the Terms of Use and Privacy Policy. Periodontium gingivaperiodontal ligamentcementumalveolus — Gums and tooth-supporting structures Cementicle Cementoblastoma Gigantiform Cementoma Eruption cyst Epulis Pyogenic granuloma Congenital epulis Gingival enlargement Gingival cyst of the adult Gingival cyst of the newborn Gingivitis Desquamative Granulomatous Plasma cell Hereditary gingival fibromatosis Hypercementosis Hypocementosis Linear gingival behcey Necrotizing periodontal diseases Acute necrotizing ulcerative gingivitis Pericoronitis Peri-implantitis Periodontal abscess Periodontal trauma Periodontitis Aggressive As a manifestation of systemic disease Chronic Perio-endo lesion Teething.

Arq Bras Oftalmol ; Prognosis In the absence of treatment, the prognosis is severe due to ocular involvement leading potentially to blindness, the risk of lethal arterial rupture and neurological symptoms potentially causing encephalopathy that may lead to a loss of autonomy.


Benign lymphoepithelial lesion Ectopic salivary gland tissue Frey’s syndrome HIV salivary gland disease Necrotizing sialometaplasia Mucocele Ranula Pneumoparotitis Salivary duct stricture Salivary gland aplasia Salivary gland atresia Salivary gland diverticulum Salivary gland fistula Salivary gland hyperplasia Salivary gland hypoplasia Salivary gland neoplasms Benign: Intracranial hypertension with papilledema may be present. Services on Demand Journal.

Lesions tend to occur in the brainstem, the basal ganglia and deep hemispheric white matter and may resemble those of MS. Chronic recurrent neutrophilic dermatosis: Sweet’s syndrome – a comprehensive review of an acute febrile neutrophilic dermatosis.

doença de Behçet

IVIG could be a treatment for severe [35] or complicated cases. Early identification and treatment is essential. Immunosuppressive therapy in connective tissue diseases-associated pulmonary dpenca hypertension.

Tromboses e aneurismas cerebrais podem ocorrer. Sulfapyridine and sulphone type drugs in dermatology.

Endovascular treatment of aortic aneurysms in patients with Behcet’s disease: report of two cases

Clinical study on death in Behcet’s disease. Orofacial soft tissues — Soft tissues around the mouth. Como sintomas adicionais haveria: Apropos of 5 new cases][Article in French]. Em comum, os tecidos variados acometidos pela DB possuem vasculite e trombose.

The person behind the eponym: Fitzpatrick’s Dermatology in General Medicine. D ICD – However, a normal study does not rule out optic neuropathy. Diagnostic methods International classification criteria, as defined by clinical df, are sensitive and specific. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.


doença de Behçet – Wiktionary

The primary mechanism of the damage is autoimmune, which by definition is an overactive immune system behvet targets the patient’s own body.

Step-up to medicine 3rd ed. Suzuki Kurokawa M, Suzuki N. Oral and maxillofacial pathology K00—K06, K11—K14—, — Anterior uveitis presents with painful eyes, conjuctival redness, hypopyonand bencet visual acuity, while posterior uveitis presents with painless decreased visual acuity and visual field floaters. Clonality in the setting of Sweet’s syndrome and pyoderma gangrenosum is not limited to underlying myeloproliferative disease.

Clinical features and treament of paristomal pyoderma gangrenosum.

Eur J Dd Dermatol Venerol. Changing patterns of uveitis. Skin ulcers misdiagnosed as pyoderma gangrenosum. An aproach to the diagnosis of neutrophilic dermatoses: N Engl J Med.