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J. vasc. bras ; 14(4): 351-355, out.-dez. 2015. tab, graf
Article in English | LILACS | ID: lil-767714

ABSTRACT

A Doença de Behçet é uma doença inflamatória caracterizada por úlceras genitais e orais recorrentes, uveítes e lesões cutâneas. O envolvimento arterial é raro, sendo mais comuns as degenerações aneurismáticas do que as oclusivas. Neste caso clínico, paciente do sexo feminino, em tratamento de doença de Behçet havia 20 anos, iniciou com dor abdominal progressiva por dois meses, com piora súbita importante, foi submetida à tomografia computadorizada, que mostrou pseudoaneurisma toracoabdominal. A paciente foi submetida a tratamento endovascular com sucesso.


Behçet’s disease is an inflammatory disease characterized by recurrent oral and genital ulcers, uveitis and skin lesions. Arterial involvement is rare, but when present aneurysmal degeneration is more common than occlusive disease. This report describes the clinical case of a female patient who had been receiving treatment for Behçet’s disease for twenty years before presenting with abdominal pain that progressed for 2 months before suddenly worsening significantly. A CT scan revealed a thoracoabdominal pseudoaneurysm. She was successfully treated with endovascular repair.


Subject(s)
Humans , Female , Adult , Aneurysm, False/rehabilitation , Endovascular Procedures/rehabilitation , Behcet Syndrome/diagnosis , Behcet Syndrome/rehabilitation , Behcet Syndrome , Prednisone/administration & dosage , Tomography, X-Ray Computed/methods
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