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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Rev Bras Cir Cardiovasc.
BJCVS, Vol.: 24 Ed.: 3 – / – , Heart transplantation in primary amyloidosis
Support All scientific articles published at www. 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. Follow-up results of a multicenter survey. One year after the heart transplantation, there was indication of renal transplantation also from the aggression from the disease.
Previous article Back to the Top Next article. The aggression to other organs, although, can make heart transplantation a disputable form of treatment taking into consideration the shortage of donor organs.
Online Submission Register here Advanced Search. The Brazilian Journal of Cardiovascular Surgery is indexed in: 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.
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. Assistant of Cardiology of Dr.
Primary tracheobronchial amyloidosis
Treatments for amyloidosis beyond symptomatic care. Combined heart and liver transplantation for familial amyloidotic polyneupathy.
J Thorac Cardiovasc Amiloidise. This patient compares’ favorable with three other patients also from our service, who died early after de diagnosis. Combined heart and liver transplantation in four adults with familial amyloidosis: 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.
Cardiovascular surgeon – Assistant of Dr. Heart transplantation in patients with amyloidosis: Progression of systemic disease an reduced long-term survival in patients with cardiac amyloidosis undergoing heart transplantation.
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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 to the cardiac transplantation, still in the evaluation stage Table 1.
Cardiac transplantation for amyloid heart disease: Recurrence of primary AL amyloidosis in a transplanted heart with four-year survival. Amiloidkse Heart Lung Transplant. Heart and liver disease in primarja patients undergoing biopsy of both organs, with implications for heart or liver transplantation.