
Pulmonary amyloidosis with calcified nodules and masses - a six-year computed tomography follow-up: a case report
2009; BioMed Central; Volume: 2; Issue: 1 Linguagem: Inglês
10.4076/1757-1626-2-6540
ISSN1757-1626
AutoresIsabela Garcia Vieira, Edson Marchiori, Gláucia Zanetti, Rafael Ferracini Cabral, Tatiana Chinem Takayassu, Gabriela Spilberg, Raquel Batista,
Tópico(s)Peptidase Inhibition and Analysis
ResumoPulmonary amyloidosis is an uncommon disease, characterized by extracellular deposition of fibrillary protein in the lungs. It appears in three forms: tracheobronchial, nodular pulmonary, and alveolar septal. There are few reports of long-term observation of primary pulmonary amyloidosis.We present the case of a 47-year-old man who presented with fever, dyspnea, cough and hemoptysis. Chest radiograph and computed tomography revealed multiple pulmonary nodules and masses. The patient underwent open lung biopsy, which diagnosed pulmonary amyloidosis.Pulmonary nodular amyloidosis should be considered in the differential diagnosis of pulmonary nodules or masses.
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