Álvaro Undurraga

Initial results with [18F]FAPI-74 PET/CT in idiopathic pulmonary fibrosis

Yuriko Mori, Vasko Kramer, Emil Novruzov, Eduards Mamlins et autres

Abstract Idiopathic pulmonary fibrosis (IPF) is a chronic fibrosing interstitial lung disease with a poor prognosis. 68 Ga-labeled FAP ligands exhibited highly promising results due to the crucial role of activated fibroblasts in fibrosis imaging of the lung. However, 18 F-labeled FAP …

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High-resolution CT phenotypes in pulmonary sarcoidosis: a multinational Delphi consensus study

Sujal R. Desai, Nishanth Sivarasan, Kerri A. Johannson, Peter M. George et autres

gb, us, ca, nz, fr, it (code pays fourni par la source)

Initial Results with [18F]FAPI-74 PET/CT in Idiopathic Pulmonary Fibrosis

Yuriko Mori, Vasko Kramer, Emil Novruzov, Eduards Mamlins et autres

Abstract Idiopathic pulmonary fibrosis (IPF) is a chronic fibrosing interstitial lung disease with a poor prognosis. 68Ga-labelled FAP ligands exhibited highly promising results due to the crucial role of activated fibroblasts in fibrosis imaging of the lung. However, 18F-labelled FAP ligands might …

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Latin American Registry of Idiopathic Pulmonary Fibrosis (REFIPI): Clinical Characteristics, Evolution and Treatment

Fabián Caro, Ivette Buendía-Roldán, Lorena Noriega, María Laura Alberti et autres

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CUADRO CLÍNICO DEL COVID-19

Rodrigo Gil, Patricia Bitar, Cristián Deza, Jorge Dreyse et autres

El Coronavirus SARS-CoV-2 produce la enfermedad COVID-19, cuya manifestación más grave y potencialmente letal es la neumonía. En este artículo revisaremos las manifestaciones clínicas del COVID-19, la fisiopatología de la neumonía, el manejo intrahospitalario previo al ingreso a Unidades de Cuidados Intensivos, …

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Enfermedades pulmonares intersticiales. Una perspectiva actual

Mauricio Salinas, Matías Florenzano, Verónica Wolff, Juan Carlos Rodrı́guez et autres

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 …

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Treatment of patients with idiopathic pulmonary fibrosis in real-life setting: Results from the Latin American Pulmonary Fibrosis Registry REFIPI

Ivette Buendía-Roldán, Pablo Curbelo, Ronaldo Adib Kairalla, Mayra Mejía et autres

Treatment of patients with IPF in real-life clinical setting: Results from the Latin American Pulmonary Fibrosis Registry (REFIPI) Introduction: Until now, we didn´t have data about anti-fibrotic management of patients with idiopathic pulmonary fibrosis (IPF) in Latin America. The REFIPI is the …

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The Latin American Idiopathic Pulmonary Fibrosis Registry (REFIPI): Baseline Characteristics

Ivette Buendía-Roldán, Fabián Caro, Pablo Curbelo, Ronaldo Adib Kairalla et autres

Background: There is an urgent need for large longitudinal registries to evaluate the long-term clinical course of IPF and impact of treatment in real-world clinical setting. In November 2017, we started the first Latin American registry (REFIPI) with participation of 11 countries. …

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Hemangioendotelioma epitelioide pulmonar: Reporte de un caso

Manuel Quiroz, Álvaro Undurraga, Rafael Díaz Moya, Cristina Fernández et autres

Epithelioid hemangioendothelioma is a multifocal tumor that rarely metastasizes. It is difficult to diagnose, most often it is an incidental finding in young asymptomatic women. The radiologic pattern is heterogeneous. Histologic confirmation of Weibel-Palade bodies or immunohistochemistry based on specific tumor markers …

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Supervivencia de pacientes con fibrosis pulmonar idiopática diagnosticados por biopsia quirúrgica de pulmón: experiencia del Instituto Nacional del Tórax

Mauricio Salinas, Matías Florenzano, Eduardo Sabbagh, Manuel Meneses et autres

BACKGROUND: Idiopathic Pulmonary Fibrosis (IPF) is the most prevalent of all interstitial lung diseases. The usual underlying pathological picture is an interstitial pneumonia (UIP). AIM: To describe the evolution of a Chilean cohort of patients with IPF. MATERIAL AND METHODS: Patients with …

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Histopathological findings of biopsies from patients with extrinsic allergic alveolitis (hipersensitivity pneumonia) in subacute or chronic phase

Mauricio Salinas, Ricardo Fritz, Manuel Meneses, Juan Carlos Díaz et autres

Introduction Extrinsic allergic alveolitis (EAA) in chronic phase is a infrequent and a disease difficult to diagnose. Biopsy findings varies and histology is an important tool for diagnosis. We present a series studied in our institution. Method We revised the pathology registries …

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Survival predictors in a cohort of patients with idiopathic pulmonary fibrosis biopsy-proven

Mauricio Salinas, Matías Florenzano, Gabriel Cavada, Álvaro Undurraga

Idiopathic Pulmonary Fibrosis (IPF) is a bad prognosis disease with heterogeneous progression. Only few studies, including relative small sample size, have searched for bad prognosis factors. The aim of this study was to analyze survival predictors in a retrospective cohort. The study …

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