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1.
Rev. méd. Chile ; 147(11): 1458-1467, nov. 2019. tab
Artículo en Español | LILACS | ID: biblio-1094176

RESUMEN

Interstitial lung diseases are a broad, diverse, challenging group of diseases, most of them chronic whose prognosis is not good. In the last two decades there have been considerable advances in the knowledge of the epidemiology, pathological and genetic bases and treatment of several of these diseases. This article summarizes and presents updated information about their classification, new knowledge on genetics and treatments in idiopathic pulmonary fibrosis, advances in the diagnosis and management of hypersensitivity pneumonitis and a review of the broad spectrum of interstitial diseases associated with connective tissue diseases. Several clinical trials are currently underway whose results will be available in the coming years and will provide more information and tools to improve the treatment of these patients.


Asunto(s)
Enfermedades Pulmonares Intersticiales/clasificación , Enfermedades Pulmonares Intersticiales/diagnóstico , Pronóstico , Enfermedades del Tejido Conjuntivo/diagnóstico , Diagnóstico Diferencial , Fibrosis Pulmonar Idiopática/diagnóstico , Alveolitis Alérgica Extrínseca/diagnóstico
2.
Rev. méd. Chile ; 145(11): 1495-1499, nov. 2017. graf
Artículo en Español | LILACS | ID: biblio-902472

RESUMEN

Lipoid pneumonia is an unusual cause of aspiration pneumonia with diverse radiologic manifestations. One of these are pulmonary nodules in which the main differential diagnosis is pulmonary carcinoma. We report an 85 years old male, an 85 years old female and a 34 years old male in whom percutaneous biopsies of suspicious nodules were compatible with lipoid pneumonia.


Asunto(s)
Humanos , Masculino , Femenino , Adulto , Anciano de 80 o más Años , Neumonía Lipoidea/diagnóstico por imagen , Neumonía Lipoidea/patología , Biopsia , Tomografía Computarizada por Rayos X
3.
Rev. méd. Chile ; 141(12): 1584-1588, dic. 2013. ilus
Artículo en Español | LILACS | ID: lil-705580

RESUMEN

In renal transplants patients, metastatic pulmonary calcifications have been reported occasionally when the grafts are dysfunctional and rarely when they are functioning normally. We report a male who received a renal allograft in 1994 at the age of 61 years. Nineteen years later a routine chest X ray showed diffuse infiltrates and a CT scan showed diffuse calcifications in both lungs. These were interpreted as metastatic pulmonary calcifications. The last available laboratory determinations were a serum creatinine of 1.4 mg/dl and urinary protein excretion of 255 mg/24 hours. No further studies were done since the patient experienced a sudden death due to an acute myocardial infarction.


Asunto(s)
Anciano de 80 o más Años , Humanos , Masculino , Calcinosis/etiología , Trasplante de Riñón/efectos adversos , Enfermedades Pulmonares/etiología , Calcinosis/diagnóstico , Creatinina/sangre , Resultado Fatal , Enfermedades Pulmonares/diagnóstico , Proteinuria/sangre , Insuficiencia Renal Crónica/complicaciones , Insuficiencia Renal Crónica/cirugía , Tomografía Computarizada por Rayos X , Trasplante Homólogo/efectos adversos
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