Resumo. A amiloidose traqueobrônquica primária é uma for- ma de amiloidose respiratória, caracterizada pela pre- sença de depósitos insolúveis de proteína. Amiloidose primaria com comprometimento meningo-radiculo-neurotico. Arquivos de. Neuro-psiquiatria (Sao Paulo), 13, Juliao, 0. al idiopathic (primary) amyloidosis. al idiopática (primaria) amiloidose. al left ear. al orellaesquerda. al porous alumni. al alumnosporosos.
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Cardiovascular surgeon – Assistant of Dr.
Primary tracheobronchial amyloidosis
Assistant of Cardiology of Dr. ABSTRACT Cardiac amyloidosis is a disease with a gloom life expectance after the beginning of the symptomatic phase, usually with sudden death as the final event. The aggression to other organs, although, can make heart transplantation a disputable form of treatment taking into consideration the shortage of donor organs.
The aim is to report the evolution with a survival of seven years after heart transplantation and in very fair condition of a patient with amyloidosis.
One year after the heart transplantation, there was indication of renal transplantation also from the aggression from the disease. This patient compares’ favorable with three other patients also from our service, who died early after de diagnosis.
Even considering the multi systemic nature of amyloidosis, we can accept that in peculiar patients justified the heart transplantation, taking in the consideration the very bad prognosis of the disease. Progression of systemic disease an reduced long-term survival in patients with cardiac amyloidosis undergoing heart transplantation.
Follow-up results of a multicenter survey. Treatments for amyloidosis beyond symptomatic care. Heart transplantation in patients with amyloidosis: Combined heart and liver transplantation for familial amyloidotic polyneupathy.
J Thorac Cardiovasc Surg. Combined heart and liver transplantation in four adults with familial amyloidosis: Recurrence of primary AL amyloidosis in a transplanted heart with four-year survival. Heart and liver disease in 32 patients undergoing biopsy of both organs, with implications for heart or liver transplantation. Cardiac transplantation for amyloid heart disease: J Heart Lung Transplant.
Rev Bras Cir Cardiovasc. Online Submission Register here Advanced Search. Even considering the multi systemic nature of amyloidosis, we can accept that in peculiar patients justified the heart transplantation, taking in the consideration the very bad prognosis of the disease Keywords Amyloidosis. Out of eight patients with cardiac amyloidosis studied, six patients presented cardiac insufficiency, three patients died in less than three months, which is in accordance with our previous experience of three cases in which all died prior primaaria the cardiac transplantation, still in the evaluation stage Table 1.
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