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.
|Published (Last):||25 November 2013|
|PDF File Size:||17.62 Mb|
|ePub File Size:||2.63 Mb|
|Price:||Free* [*Free Regsitration Required]|
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.
Rev Bras Cir Cardiovasc. J Heart Lung Transplant. Online Submission Register here Advanced Search.
Primary tracheobronchial amyloidosis
Cardiac transplantation for amyloid heart disease: Combined heart and liver transplantation in four adults with familial amyloidosis: The aggression to other organs, although, can make heart transplantation a disputable form of treatment taking into consideration the shortage of donor organs. J Thorac Cardiovasc Surg. Cardiovascular surgeon – Assistant of Dr.
Combined heart and liver transplantation for familial amyloidotic polyneupathy.
Heart and liver disease in 32 patients undergoing biopsy of both organs, with implications for heart or liver transplantation. One year after the heart transplantation, there was indication of renal transplantation also from the aggression from the disease.
There was a problem providing the content you requested
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.
Assistant of Cardiology of Dr. 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. 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.
This patient compares’ favorable with three other patients also from our service, ajiloidose died early after de diagnosis.
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. Previous article Back to the Top Next article.
The Brazilian Journal of Cardiovascular Surgery is indexed in: Progression of systemic disease an reduced long-term survival in patients with cardiac amyloidosis undergoing heart transplantation. Recurrence of primary AL amyloidosis in a transplanted heart with four-year survival.
Support All scientific articles published at www. Follow-up results of a multicenter survey.
Heart transplantation in patients with amyloidosis: Treatments for amyloidosis beyond symptomatic care.