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1.
Eur J Nucl Med Mol Imaging ; 51(6): 1605-1611, 2024 May.
Article in English | MEDLINE | ID: mdl-38117298

ABSTRACT

Idiopathic pulmonary fibrosis (IPF) is a chronic fibrosing interstitial lung disease with a poor prognosis. 68Ga-labeled FAP ligands exhibited highly promising results due to the crucial role of activated fibroblasts in fibrosis imaging of the lung. However, 18F-labeled FAP ligands might provide qualitatively much higher imaging results with accompanying economic benefits due to large-scale production. Thus, we sought to investigate the potential of [18F]FAPI-74 prospectively in a small patient cohort. METHODS: Eight patients underwent both [18F]FAPI-74-PET/CT and HRCT scans and were then compared with a control group without any fibrosing pulmonary disease. The tracer uptake of fibrotic lung areas was analyzed in synopsis with radiological and clinical parameters. RESULTS: We observed a positive correlation between the fibrotic active volume, the Hounsfield scale, as well as the vital and diffusing capacity of the lung. CONCLUSION: The initial results confirm our assumption that [18F]FAPI-74 offers a viable non-invasive assessment method for pulmonary fibrotic changes in patients with IPF.


Subject(s)
Idiopathic Pulmonary Fibrosis , Positron Emission Tomography Computed Tomography , Humans , Idiopathic Pulmonary Fibrosis/diagnostic imaging , Male , Female , Aged , Middle Aged , Lung/diagnostic imaging
2.
Respirology ; 20(6): 873-83, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25998242

ABSTRACT

The 2013 American Thoracic Society/European Respiratory Society consensus classification update of the idiopathic interstitial pneumonias (IIP) included several important modifications to the organization and spectrum of the diseases that were proposed in an earlier multidisciplinary consensus document in 2002. The histopathology of the now 'major' and 'rare' IIP is presented here with exposition of the newly included entity of a distinctive upper lobe fibrotic lung disease referred to as idiopathic pleuroparenchymal fibroelastosis. The 'rare histological patterns' of acute fibrinous and organizing pneumonia and bronchiolocentric patterns of interstitial pneumonia are illustrated and discussed.


Subject(s)
Idiopathic Interstitial Pneumonias/pathology , Diagnosis, Differential , Humans
3.
Rev Chilena Infectol ; 31(2): 139-52, 2014 Apr.
Article in Spanish | MEDLINE | ID: mdl-24878902

ABSTRACT

INTRODUCTION: The population of immunocompromised patients has increased in recent decades. Many of these patients eventually present infectious complications including pneumonia, which is a diagnostic that must to be prompt and accurate. OBJECTIVE: To review the basis of the diagnosis of pneumonia in the immunocompromised patient. Sorted by the methodology of Bayesian inference, very relevant in the diagnostic attribution, we review the main basis of the diagnosis of pneumonia of immunocompromised patients: the epidemiology, the clinical history including the type of immunosuppression that weigh the likelihood of attribution a priori of an etiologic agent, and finally, the findings in the image (or likelihood function). CONCLUSION: Although in general the findings are not pathognomonic and there is much overlap in the images, there are several features that orient in one direction or another. Proper assessment of the prior probability and the likelihood function is allowing ultimately a good diagnostic proposition.


Subject(s)
Immunocompromised Host/immunology , Pneumonia/microbiology , Bayes Theorem , Female , Humans , Likelihood Functions , Male , Pneumonia/diagnostic imaging , Pneumonia/immunology , Radiography
4.
Rev Med Chil ; 142(1): 9-15, 2014 Jan.
Article in Spanish | MEDLINE | ID: mdl-24861108

ABSTRACT

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 the disease were identified at the pathology registry of National Institute of Thoracic Diseases, Santiago, Chile. Patients were included if they had surgical biopsy of UIP and compatible clinical and radiological characteristics. The medical records of included patients were reviewed, recording clinical information and lung function test results. Survival was analyzed obtaining death records from the Chilean National Identification Service. RESULTS: Data from 142 patients with a mean age of 58 years (42% men), were analyzed. Mean initial lung function showed a forced vital capacity (FVC) of 73%, carbon monoxide diffusing capacity (DLCO) of 57% and a distance covered in 6-minute walk (6MWT) of 95% of expected normal values. The median survival was 80 months. Predictors of survival were a DLCO of less than 40% and an oxygen saturation at the end of the 6MWT of less than 89%. CONCLUSIONS: Survival in this group of patients was higher than the figures reported elsewhere. DLCO and the fall of oxygen saturation after walking were predictors of mortality, as previously described in other populations.


Subject(s)
Idiopathic Pulmonary Fibrosis/mortality , Biopsy , Cohort Studies , Female , Humans , Idiopathic Pulmonary Fibrosis/pathology , Lung/pathology , Male , Middle Aged , Respiratory Function Tests , Retrospective Studies , Survival Analysis
5.
Rev. chil. infectol ; 31(2): 139-152, abr. 2014. ilus, tab
Article in Spanish | LILACS | ID: lil-708800

ABSTRACT

Introduction: The population of immunocompromised patients has increased in recent decades. Many of these patients eventually present infectious complications including pneumonia, which is a diagnostic that must to be prompt and accurate. Objective: To review the basis of the diagnosis of pneumonia in the immunocompromised patient. Sorted by the methodology of Bayesian inference, very relevant in the diagnostic attribution, we review the main basis of the diagnosis of pneumonia of immunocompromised patients: the epidemiology, the clinical history including the type of immunosuppression that weigh the likelihood of attribution a priori of an etiologic agent, and finally, the findings in the image (or likelihood function). Conclusion: Although in general the findings are not pathognomonic and there is much overlap in the images, there are several features that orient in one direction or another. Proper assessment of the prior probability and the likelihood function is allowing ultimately a good diagnostic proposition.


Introducción: La población de pacientes inmunocomprometidos se ha incrementado en las últimas décadas. Gran parte de estos pacientes presenta en algún momento complicaciones infecciosas, entre ellas la neumonía, lo que constituye un desafío diagnóstico que debe ser rápido y acertado. Objetivo: Revisar las bases del diagnóstico de las neumonías del paciente inmunocomprometido. Ordenados por la metodología de la inferencia Bayesiana, muy relevante en la atribución diagnóstica, destacamos y revisamos los pilares fundamentales en el diagnóstico de las neumonías del inmunocomprometido: la epidemiología, los antecedentes clínicos incluyendo el tipo de inmunodepresión, que pesan en la probabilidad de atribución a priori de un agente etiológico, y finalmente, los hallazgos en la imagen (o función de verosimilitud). Conclusión: Los hallazgos de imagen que, aunque en general no son patognomónicos y existe mucha superposición, presentan algunas características que orientan en una u otra dirección. La adecuada valoración de la probabilidad a priori y la función de verosimilitud son las que permiten en definitiva una buena proposición diagnóstica.


Subject(s)
Female , Humans , Male , Immunocompromised Host/immunology , Pneumonia/microbiology , Bayes Theorem , Likelihood Functions , Pneumonia/immunology , Pneumonia
6.
Rev. méd. Chile ; 142(1): 9-15, ene. 2014. ilus, graf, tab
Article in Spanish | LILACS | ID: lil-708844

ABSTRACT

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 the disease were identified at the pathology registry of National Institute of Thoracic Diseases, Santiago, Chile. Patients were included if they had surgical biopsy of UIP and compatible clinical and radiological characteristics. The medical records of included patients were reviewed, recording clinical information and lung function test results. Survival was analyzed obtaining death records from the Chilean National Identification Service. Results: Data from 142 patients with a mean age of 58 years (42% men), were analyzed. Mean initial lung function showed a forced vital capacity (FVC) of 73%, carbon monoxide diffusing capacity (DLCO) of 57% and a distance covered in 6-minute walk (6MWT) of 95% of expected normal values. The median survival was 80 months. Predictors of survival were a DLCO of less than 40% and an oxygen saturation at the end of the 6MWT of less than 89%. Conclusions: Survival in this group of patients was higher than the figures reported elsewhere. DLCO and the fall of oxygen saturation after walking were predictors of mortality, as previously described in other populations.


Subject(s)
Female , Humans , Male , Middle Aged , Idiopathic Pulmonary Fibrosis/mortality , Biopsy , Cohort Studies , Idiopathic Pulmonary Fibrosis/pathology , Lung/pathology , Respiratory Function Tests , Retrospective Studies , Survival Analysis
7.
Rev Med Chil ; 132(4): 489-92, 2004 Apr.
Article in Spanish | MEDLINE | ID: mdl-15382522

ABSTRACT

Arterial embolization with cyanoacrylate is commonly used for the treatment of arteriovenous malformations. We report the case of a 40 years old man who four days after an embolization with cyanoacrylate, begins with cough, bloody sputum, and right hemithorax pleuritic pain. Pulmonary embolism was confirmed with chest X ray, CT scan and scyntigraphy. The patient received anticoagulation, with adequate response. The most common complications of cerebral embolization are related to central nervous system and pulmonary embolism is exceptional. Considering the high number of embolization procedures done nowadays, this complication must be borne in mind.


Subject(s)
Cyanoacrylates/adverse effects , Embolization, Therapeutic/adverse effects , Intracranial Arteriovenous Malformations/therapy , Pulmonary Embolism/etiology , Adult , Chest Pain/etiology , Humans , Male , Radiography, Thoracic , Tomography, X-Ray Computed
8.
Rev. méd. Chile ; 132(4): 489-492, abr. 2004. ilus
Article in Spanish | LILACS | ID: lil-362915

ABSTRACT

Arterial embolization with cyanoacrylate is commonly used for the treatment of arteriovenous malformations. We report the case of a 40 years old man who four days after an embolization with cyanoacrylate, begins with cough, bloody sputum, and right hemithorax pleuritic pain. Pulmonary embolism was confirmed with chest X ray, CT scan and scyntigraphy. The patient received anticoagulation, with adequate response. The most common complications of cerebral embolization are related to central nervous system and pulmonary embolism is exceptional. Considering the high number of embolization procedures done nowadays, this complication must be borne in mind.


Subject(s)
Humans , Male , Cyanoacrylates/therapeutic use , Pulmonary Embolism/complications , Pulmonary Embolism/etiology , Pulmonary Embolism/therapy , Embolization, Therapeutic/adverse effects , Intracranial Arteriovenous Malformations/therapy , Intracranial Embolism , Pulmonary Embolism
12.
In. Sociedad Médica de Santiago. Curso 1994: problemas frecuentes en la atención primaria del adulto. Santiago, Sociedad Médica de Santiago, 1994. p.81-2.
Monography in Spanish | LILACS | ID: lil-152758
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