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Journal articles on the topic 'Diffuse parenchymal lung diseases'

Author: Grafiati

Published: 4 June 2021

Last updated: 13 February 2022

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1

Tomassetti, Sara, Claudia Ravaglia, and Venerino Poletti. "Diffuse parenchymal lung disease." European Respiratory Review 26, no. 144 (2017): 170004. http://dx.doi.org/10.1183/16000617.0004-2017.

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Between September 2015 and August 2016 there were >1500 publications in the field of diffuse parenchymal lung diseases (DPLDs). For the Clinical Year in Review session at the European Respiratory Society Congress that was held in London, UK, in September 2016, we selected only five articles. This selection, made from the enormous number of published papers, does not include all the relevant studies that will significantly impact our knowledge in the field of DPLDs in the near future. This review article provides our personal view on the following topics: early diagnosis of idiopathic pulmon

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2

Poletti, Venerino, Claudia Ravaglia, and Sara Tomassetti. "Transbronchial cryobiopsy in diffuse parenchymal lung diseases." Current Opinion in Pulmonary Medicine 22, no. 3 (2016): 289–96. http://dx.doi.org/10.1097/mcp.0000000000000272.

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3

Martinez, Fernando J., and Michael P. Keane. "Update in Diffuse Parenchymal Lung Diseases 2005." American Journal of Respiratory and Critical Care Medicine 173, no. 10 (2006): 1066–71. http://dx.doi.org/10.1164/rccm.2601011.

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4

Raghunath, Sushravya, Srinivasan Rajagopalan, Ronald A. Karwoski, et al. "Quantitative Stratification of Diffuse Parenchymal Lung Diseases." PLoS ONE 9, no. 3 (2014): e93229. http://dx.doi.org/10.1371/journal.pone.0093229.

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5

Walsh, Sinead M., and Anthony W. O’Regan. "Diffuse Parenchymal Lung Diseases in the Elderly." Current Geriatrics Reports 7, no. 3 (2018): 174–80. http://dx.doi.org/10.1007/s13670-018-0249-x.

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6

Shlobin, Oksana A., A. Whitney Brown, and Steven D. Nathan. "Pulmonary Hypertension in Diffuse Parenchymal Lung Diseases." Chest 151, no. 1 (2017): 204–14. http://dx.doi.org/10.1016/j.chest.2016.08.002.

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7

Farag, TaghreedS, ZeinabR Adawy, LobnaK Sakr, and HanaaS Abdellateef. "Transthoracic ultrasonographic features of diffuse parenchymal lung diseases." Egyptian Journal of Bronchology 11, no. 3 (2017): 179. http://dx.doi.org/10.4103/ejb.ejb_3_17.

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8

Tsangaris, Iraklis, Georgios Tsaknis, Anastasia Anthi, and Stylianos E. Orfanos. "Pulmonary Hypertension in Parenchymal Lung Disease." Pulmonary Medicine 2012 (2012): 1–14. http://dx.doi.org/10.1155/2012/684781.

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Idiopathic pulmonary arterial hypertension (IPAH) has been extensively investigated, although it represents a less common form of the pulmonary hypertension (PH) family, as shown by international registries. Interestingly, in types of PH that are encountered in parenchymal lung diseases such as interstitial lung diseases (ILDs), chronic obstructive pulmonary disease (COPD), and many other diffuse parenchymal lung diseases, some of which are very common, the available data is limited. In this paper, we try to browse in the latest available data regarding the occurrence, pathogenesis, and treatm

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Braun, Sarah, Marion Ferner, Kai Kronfeld, and Matthias Griese. "Hydroxychloroquine in children with interstitial (diffuse parenchymal) lung diseases." Pediatric Pulmonology 50, no. 4 (2014): 410–19. http://dx.doi.org/10.1002/ppul.23133.

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10

Pulagam, Ammi Reddy, Giri Babu Kande, Venkata Krishna Rao Ede, and Ramesh Babu Inampudi. "Automated Lung Segmentation from HRCT Scans with Diffuse Parenchymal Lung Diseases." Journal of Digital Imaging 29, no. 4 (2016): 507–19. http://dx.doi.org/10.1007/s10278-016-9875-z.

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11

Baldi, Bruno Guedes, Carlos Roberto Ribeiro Carvalho, Olívia Meira Dias, Edson Marchiori, and Bruno Hochhegger. "Diffuse cystic lung diseases: differential diagnosis." Jornal Brasileiro de Pneumologia 43, no. 2 (2017): 140–49. http://dx.doi.org/10.1590/s1806-37562016000000341.

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ABSTRACT Diffuse cystic lung diseases are characterized by cysts in more than one lung lobe, the cysts originating from various mechanisms, including the expansion of the distal airspaces due to airway obstruction, necrosis of the airway walls, and parenchymal destruction. The progression of these diseases is variable. One essential tool in the evaluation of these diseases is HRCT, because it improves the characterization of pulmonary cysts (including their distribution, size, and length) and the evaluation of the regularity of the cyst wall, as well as the identification of associated pulmona

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12

Batra, Kiran, Riham Dessouky, YasmeenM Butt, Vibhor Wadhwa, JoseR Torrealba, and Craig Glazer. "Series of rare lung diseases mimicking imaging patterns of common diffuse parenchymal lung diseases." Lung India 35, no. 3 (2018): 231. http://dx.doi.org/10.4103/lungindia.lungindia_291_17.

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13

Narender, Methuku, Manikanta Dhanamurthy Koppu, Vavilala Satish Kumar Rao, Auzumeedi Sai Kumar, Subhakar Kandi, and Surya Kiran Pulivarthi. "ROLE OF TRANS BRON CHIAL LUNG BIOPSY IN DIFFUSE PARENCHYMAL LUNG DISEASES." Journal of Evolution of Medical and Dental Sciences 4, no. 69 (2015): 11924–30. http://dx.doi.org/10.14260/jemds/2015/1721.

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14

Dikensoy, Oner, Resat Kervancioglu, Ibrahim Ege, Nevin Uysal, Osman Elbek, and Ayhan Ozkur. "High Prevalence of Diffuse Parenchymal Lung Diseases among Turkish Tinners." Journal of Occupational Health 50, no. 2 (2008): 208–11. http://dx.doi.org/10.1539/joh.l7104.

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15

Cinel, Güzin, Nural Kiper, Diclehan Orhan, et al. "Childhood diffuse parenchymal lung diseases: We need a new classification." Clinical Respiratory Journal 14, no. 2 (2019): 102–8. http://dx.doi.org/10.1111/crj.13106.

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16

Kln??, G??nseli, and Elif Altu?? Kolsuk. "The role of bronchoalveolar lavage in diffuse parenchymal lung diseases." Current Opinion in Pulmonary Medicine 11, no. 5 (2005): 417–21. http://dx.doi.org/10.1097/01.mcp.0000175522.49353.e1.

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17

Meng, Peng, Gan Liang Tan, Su Ying Low, Angela Takano, Yuen Li Ng, and Devanand Anantham. "Fibered Confocal Fluorescence Microscopy Imaging in Diffuse Parenchymal Lung Diseases." Chest 148, no. 4 (2015): 788A. http://dx.doi.org/10.1378/chest.2254272.

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18

Canıvar, Coşkun, Züleyha Bingöl, Zeki Kılıçaslan, Tülin Çağatay, and N. Gülfer Okumuş. "Investigation of parameters related to prognosis in diffuse parenchymal lung diseases prognosis in interstitial lung diseases." Tuberkuloz ve Toraks 65, no. 3 (2017): 210–19. http://dx.doi.org/10.5578/tt.57501.

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19

Alapati, Deepthi, William J. Zacharias, Heather A. Hartman, et al. "In utero gene editing for monogenic lung disease." Science Translational Medicine 11, no. 488 (2019): eaav8375. http://dx.doi.org/10.1126/scitranslmed.aav8375.

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Monogenic lung diseases that are caused by mutations in surfactant genes of the pulmonary epithelium are marked by perinatal lethal respiratory failure or chronic diffuse parenchymal lung disease with few therapeutic options. Using a CRISPR fluorescent reporter system, we demonstrate that precisely timed in utero intra-amniotic delivery of CRISPR-Cas9 gene editing reagents during fetal development results in targeted and specific gene editing in fetal lungs. Pulmonary epithelial cells are predominantly targeted in this approach, with alveolar type 1, alveolar type 2, and airway secretory cells

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20

Ghigna, Maria Rosa, Wolter J. Mooi, and Katrien Grünberg. "Pulmonary hypertensive vasculopathy in parenchymal lung diseases and/or hypoxia." European Respiratory Review 26, no. 144 (2017): 170003. http://dx.doi.org/10.1183/16000617.0003-2017.

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Pulmonary hypertension (PH) with complicating chronic lung diseases and/or hypoxia falls into group 3 of the updated classification of PH. Patients with chronic obstructive lung disease (COPD), diffuse lung disease (such as idiopathic pulmonary fibrosis (IPF)) and with sleep disordered breathing are particularly exposed to the risk of developing PH. Although PH in such a context is usually mild, a minority of patients exhibit severe haemodynamic impairment, defined by a mean pulmonary arterial pressure (mPAP) of ≥35 mmHg or mPAP values ranging between 25 mmHg and 35 mmHg with a low cardiac ind

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21

ÇIRAK, Ali Kadri, Nuran KATGI, Onur Fevzi ERER, Pınar ÇİMEN, Fatma Fevziye TUKSAVUL, and Burçin HAKOĞLU. "Diagnostic approach in parenchymal lung diseases: transbronchial lung biopsy or cryobiopsy?" TURKISH JOURNAL OF MEDICAL SCIENCES 50, no. 6 (2020): 1535–39. http://dx.doi.org/10.3906/sag-1910-47.

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Background/aim: Diagnosis of interstitial lung diseases requires a multidisciplinary approach, and a gold standard for histological diagnosis is open lung biopsy. Transbronchial lung biopsy (TBLB) and in recent years an alternative method, cryobiopsy (TBLC), are used for the diagnosis of parenchymal lung lesions. The aim of this study is to compare the efficacy of concomitant conventional TBLB and TBLC.Materials and methods: A total of 82 patients who underwent TBLC for diagnosis of diffuse parenchymal lung diseases at Dr. Suat Seren Chest Diseases and Surgery Training and Research Hospital be

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22

Abdelsalam, Etemad, MagdyM Omar, AhmadS Alhalafawy, NashwaM Emara, and MohammadA E. El-Mahdy. "The role of medical thoracoscopic lung biopsy in diagnosis of diffuse parenchymal lung diseases." Egyptian Journal of Bronchology 13, no. 2 (2019): 155. http://dx.doi.org/10.4103/ejb.ejb_41_18.

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23

Shafiek, Hanaa, Shaimaa Elbialy, Samar Nabil Elachy, and Ahmed Youssef Gad. "Transbronchial cryobiopsy validity in diagnosing diffuse parenchymal lung diseases in Egyptian population." Journal of Multidisciplinary Healthcare Volume 12 (August 2019): 719–26. http://dx.doi.org/10.2147/jmdh.s208824.

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24

Yadav, Dr Harendra, and Dr Rahul Srivastava. "Clinicoradiological and demographic pattern in diffuse parenchymal lung diseases: An observational study." International Journal of Medical Research and Review 6, no. 6 (2018): 308–14. http://dx.doi.org/10.17511/ijmrr.2018.i06.03.

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25

Verrastro, Carlos Gustavo Yuji, Viviane Baptista Antunes, Dany Jasinowodolinski, Giuseppe DʼIppolito, and Gustavo de Souza Portes Meirelles. "High-Resolution Computed Tomography in the Diagnosis of Diffuse Parenchymal Lung Diseases." Journal of Computer Assisted Tomography 40, no. 2 (2016): 248–55. http://dx.doi.org/10.1097/rct.0000000000000344.

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26

Kulshrestha, Ritu, Himanshu Dhanda, Apoorva Pandey, Amit Singh, and Raj Kumar. "Immunopathogenesis and therapeutic potential of macrophage influx in diffuse parenchymal lung diseases." Expert Review of Respiratory Medicine 14, no. 9 (2020): 917–28. http://dx.doi.org/10.1080/17476348.2020.1776117.

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27

Urban, Jan, Magda Suchankova, Martina Ganovska, et al. "The Role of CX3CL1 and ADAM17 in Pathogenesis of Diffuse Parenchymal Lung Diseases." Diagnostics 11, no. 6 (2021): 1074. http://dx.doi.org/10.3390/diagnostics11061074.

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Fractalkine (CX3CL1) is a unique chemokine that functions as a chemoattractant for effector cytotoxic lymphocytes and macrophages expressing fractalkine receptor CX3CR1. CX3CL1 exists in two forms—a soluble and a membrane-bound form. The soluble CX3CL1 is released from cell membranes by proteolysis by the TNF-α-converting enzyme/disintegrin-like metalloproteinase 17 (TACE/ADAM17) and ADAM10. In this study, we evaluated the diagnostic relevance and potential roles of CX3CL1 and ADAM17 in the pathogenesis of diffuse parenchymal lung diseases (DPLDs) in the human population. The concentration of

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28

Viglietta, Luca, Riccardo Inchingolo, Cristina Pavano, et al. "Ultrasonography for the Diagnosis of Pneumothorax after Transbronchial Lung Cryobiopsy in Diffuse Parenchymal Lung Diseases." Respiration 94, no. 2 (2017): 232–36. http://dx.doi.org/10.1159/000477818.

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29

Wuyts, Wim. "Surgical lung biopsy is not the golden standard in diagnosis of diffuse parenchymal lung diseases." European Journal of Cardio-Thoracic Surgery 34, no. 6 (2008): 1271–72. http://dx.doi.org/10.1016/j.ejcts.2008.09.018.

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30

Bondue, Benjamin, Thierry Pieters, Patrick Alexander, et al. "Role of Transbronchial Lung Cryobiopsies in Diffuse Parenchymal Lung Diseases: Interest of a Sequential Approach." Pulmonary Medicine 2017 (2017): 1–7. http://dx.doi.org/10.1155/2017/6794343.

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Background. Transbronchial lung cryobiopsies (TBLCs) are a promising diagnostic tool in the setting of diffuse parenchymal lung diseases (DPLDs). However, no comparison with surgical lung biopsy (SLB) in the same patient is available. Methods. The diagnostic yield and safety data of TBLCs, as well as the result of SLB performed after TBLCs, were analysed in a multicentric Belgian study. A SLB was performed after TBLCs in absence of a definite pathological diagnosis or if a NSIP pattern was observed without related condition identified following multidisciplinary discussion. Results. Between Ap

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31

Biswas, Muhammad Asaduzzaman, Muhammad Nazrul Islam, Khalifa Mahmud Walid, and Zhilam Zia Rassel. "Case Report of Diffuse Parenchymal Lung Disease with Non-Specific Interstitial Pneumonia Pattern and Good Response to Treatment." Faridpur Medical College Journal 13, no. 2 (2019): 101–3. http://dx.doi.org/10.3329/fmcj.v13i2.43646.

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The diffuse parenchymal lung diseases (DPLDs) are a heterogeneous group of conditions affecting the pulmonary parenchyma (interstitial) and/or alveolar lumen. IPF (Idiopathic Pulmonary Fibrosis) is a chronic interstitial pneumonia of unknown causes. It is commonest form of DPLD but its treatment response is very poor. On the other hand, NSIP (Non-Specific Interstitial Pneumonia) can still be a variant of DPLD with better treatment response and prognosis. Here we discussed a young female with NSIP with good response to steroid. Faridpur Med. Coll. J. Jul 2018;13(2): 101-103

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32

Aboudara, Matthew, and Fabien Maldonado. "Transbronchial cryobiopsy for diffuse parenchymal lung diseases: evidence that demands a (favorable) verdict." Annals of Translational Medicine 8, no. 20 (2020): 1324. http://dx.doi.org/10.21037/atm-20-2995.

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33

Li, Diandian, Bo Wang, Yi Liu, and Haohua Wang. "Prevalence and impact of comorbid obstructive sleep apnoea in diffuse parenchymal lung diseases." PLOS ONE 16, no. 2 (2021): e0246878. http://dx.doi.org/10.1371/journal.pone.0246878.

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Objective Obstructive sleep apnea (OSA) are increasingly recognized as important features in diffuse parenchymal lung diseases (DPLDs) with differed prevalence and impact reported. The aim of this study is to systematically review the prevalence of comorbid OSA and characterize its impact on clinical and outcome measurements in adults with DPLDs. Methods Publications addressing the prevalence of OSA in DPLDs and its impacts on DPLDs were selected from electronic databases. A random-effect model was used to estimate the pooled prevalence of OSA. Odds ratios (ORs) or mean differences (MDs) were

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34

Alfaro, Tiago M., Catharina C. Moor, Veronica Alfieri, et al. "Research highlights from the 2018 ERS International Congress: interstitial lung diseases." ERJ Open Research 5, no. 1 (2019): 00215–2018. http://dx.doi.org/10.1183/23120541.00215-2018.

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This article reviews a selection of the scientific presentations on interstitial lung disease (ILD)/diffuse parenchymal lung disease (DPLD) that were made at the 2018 European Respiratory Society (ERS) International Congress in Paris. A number of advances in the epidemiology, pathogenesis, diagnosis and treatment of these disorders were presented and discussed by clinicians and researchers. The research topics span over all four groups of ERS Assembly 12: Interstitial Lung Diseases (Group 12.01: Idiopathic interstitial pneumonias; Group 12.02: ILD/DPLD of known origin; Group 12.03: Sarcoidosis

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35

Aquilina, Giulia, Daniele Carmelo Caltabiano, Federica Galioto, et al. "Cystic Interstitial Lung Diseases: A Pictorial Review and a Practical Guide for the Radiologist." Diagnostics 10, no. 6 (2020): 346. http://dx.doi.org/10.3390/diagnostics10060346.

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A cyst is a round circumscribed area of low attenuation, surrounded by epithelial or fibrous wall. Cysts can frequently occur on chest computed tomography (CT) and high-resolution computed tomography (HRCT); multiple parenchymal cysts of the lungs are the most typical feature of cystic lung interstitial diseases, characterizing a wide spectrum of diseases—ranging from isolated lung disorders up to diffuse pulmonary diseases. The aim of this review is to analyze scientific literature about cystic lung interstitial diseases and to provide a practical guide for radiologists, focusing on the main

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36

Cony, Fernanda G., Fernando F. Argenta, Lilian C. Heck, et al. "Clinical and pathological aspects of idiopathic pulmonary fibrosis in cats." Pesquisa Veterinária Brasileira 39, no. 2 (2019): 134–41. http://dx.doi.org/10.1590/1678-5150-pvb-5942.

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ABSTRACT: Interstitial lung diseases are a group of diffuse parenchymal lung diseases that include interstitial lung fibrosis. The aim of this study is to characterize the clinical and pathological findings of idiopathic pulmonary fibrosis in three cats and to investigate possible etiological agents through bacteriological and mycological exams and immunohistochemistry. All three cats were female and aged from 10 to 14 years old, they presented with a clinical history of weight loss and dyspnea. The radiographic changes were similar in all cats and included increased pulmonary radiopacity with

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37

KARADOĞAN, Dilek, and Göksel ALTINIŞIK. "The Evaluation of Patients Diagnosed as Diffuse Parenchymal Lung Diseases Between Years 2005-2010." Turkiye Klinikleri Journal of Health Sciences 4, no. 1 (2019): 34–42. http://dx.doi.org/10.5336/healthsci.2018-62248.

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38

Casoni, G. L., C. R. Cordeiro, S. Tomassetti, et al. "The role of transbronchial biopsy in the diagnosis of diffuse parenchymal lung diseases: Pro." Revista Portuguesa de Pneumologia (English Edition) 18, no. 2 (2012): 57–60. http://dx.doi.org/10.1016/j.rppnen.2011.03.004.

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39

Margaritopoulos, G. A., and A. U. Wells. "The role of transbronchial biopsy in the diagnosis of diffuse parenchymal lung diseases: Con." Revista Portuguesa de Pneumologia (English Edition) 18, no. 2 (2012): 61–63. http://dx.doi.org/10.1016/j.rppnen.2011.09.005.

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40

Casoni, G. L., C. R. Cordeiro, S. Tomassetti, et al. "The role of transbronchial biopsy in the diagnosis of diffuse parenchymal lung diseases: Pro." Revista Portuguesa de Pneumologia 18, no. 2 (2012): 57–60. http://dx.doi.org/10.1016/j.rppneu.2011.05.003.

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41

Margaritopoulos, G. A., and A. U. Wells. "The role of transbronchial biopsy in the diagnosis of diffuse parenchymal lung diseases: Con." Revista Portuguesa de Pneumologia 18, no. 2 (2012): 61–63. http://dx.doi.org/10.1016/j.rppneu.2011.09.004.

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42

Maldonado, Fabien, and Jay H. Ryu. "Surgical Biopsy for Diffuse Parenchymal Lung Diseases: Are We Causing More Harm Than Good?" Journal of Bronchology & Interventional Pulmonology 16, no. 4 (2009): 227–28. http://dx.doi.org/10.1097/lbr.0b013e3181bb7371.

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43

Samarelli, Anna Valeria, Roberto Tonelli, Alessandro Marchioni, et al. "Fibrotic Idiopathic Interstitial Lung Disease: The Molecular and Cellular Key Players." International Journal of Molecular Sciences 22, no. 16 (2021): 8952. http://dx.doi.org/10.3390/ijms22168952.

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Interstitial lung diseases (ILDs) that are known as diffuse parenchymal lung diseases (DPLDs) lead to the damage of alveolar epithelium and lung parenchyma, culminating in inflammation and widespread fibrosis. ILDs that account for more than 200 different pathologies can be divided into two groups: ILDs that have a known cause and those where the cause is unknown, classified as idiopathic interstitial pneumonia (IIP). IIPs include idiopathic pulmonary fibrosis (IPF), non-specific interstitial pneumonia (NSIP), cryptogenic organizing pneumonia (COP) known also as bronchiolitis obliterans organi

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44

Ryu, Jay H., Teng Moua, Natalya Azadeh, Misbah Baqir, and Eunhee S. Yi. "Current concepts and dilemmas in idiopathic interstitial pneumonias." F1000Research 5 (November 10, 2016): 2661. http://dx.doi.org/10.12688/f1000research.9601.1.

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Idiopathic interstitial pneumonias comprise approximately one-third of interstitial lung diseases (also called diffuse parenchymal infiltrative lung diseases). The classification of idiopathic interstitial pneumonias has undergone several revisions since the initial description of 40 years ago, and the most recent version was published in 2013. Although some aspects have been clarified, this group of heterogeneous disorders continues to be a source of confusion and misunderstanding in clinical applications. In this article, we explore several topical themes in the evaluation and management of

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45

Szturmowicz, Monika, Aneta Kacprzak, and Jan Kuś. "Pulmonary hypertension in diffuse parenchymal lung diseases — is there any benefit of PAH-specific therapy?" Advances in Respiratory Medicine 85, no. 4 (2017): 216–23. http://dx.doi.org/10.5603/arm.2017.0036.

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46

Xu, Dan, Zhimin Chen, Huizhong Chen, et al. "Application of Clinico-Radiologic-Pathologic Diagnosis of Diffuse Parenchymal Lung Diseases in Children in China." PLOS ONE 10, no. 1 (2015): e0116930. http://dx.doi.org/10.1371/journal.pone.0116930.

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47

Flamein, Florence, Laure Riffault, Céline Muselet-Charlier, et al. "Molecular and cellular characteristics of ABCA3 mutations associated with diffuse parenchymal lung diseases in children." Human Molecular Genetics 21, no. 4 (2011): 765–75. http://dx.doi.org/10.1093/hmg/ddr508.

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48

Wuyts, Wim A., and Geert M. Verleden. "Integration of Clinical, Radiological, and Histopathological Data in the Diagnosis of Diffuse Parenchymal Lung Diseases." American Journal of Respiratory and Critical Care Medicine 179, no. 3 (2009): 254–55. http://dx.doi.org/10.1164/ajrccm.179.3.254b.

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49

MASSOPTIER, LAURENT, AVISHKAR MISRA, ARCOT SOWMYA, and SERGIO CASCIARO. "COMBINING GRAPH-CUT TECHNIQUE AND ANATOMICAL KNOWLEDGE FOR AUTOMATIC SEGMENTATION OF LUNGS AFFECTED BY DIFFUSE PARENCHYMAL DISEASE IN HRCT IMAGES." International Journal of Image and Graphics 11, no. 04 (2011): 509–29. http://dx.doi.org/10.1142/s0219467811004202.

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Accurate and automated lung segmentation in high-resolution computed tomography (HRCT) is highly challenged by the presence of pathologies affecting lung parenchyma appearance and borders. The algorithm presented employs an anatomical model-driven approach and systematic incremental knowledge acquisition to produce coarse lung delineation, used as initialization for the graph-cut algorithm. The proposed method is evaluated on a 49 HRCT cases dataset including various lung disease patterns. The accuracy of the method is assessed using dice similarity coefficient (DSC) and shape differentiation

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50

Dupin, Clairelyne, Vânia Fernandes, Fernanda Hernandez-Gonzalez, et al. "ERS International Congress, Madrid, 2019: highlights from the Interstitial Lung Diseases Assembly." ERJ Open Research 6, no. 4 (2020): 00143–2020. http://dx.doi.org/10.1183/23120541.00143-2020.

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This article discusses a selection of the scientific presentations in the field of interstitial lung diseases (ILDs) that took place at the 2019 European Respiratory Society International Congress in Madrid, Spain. There were sessions from all four groups within Assembly 12: group 12.01 “Idiopathic interstitial pneumonias”, group 12.02 “ILDs/diffuse parenchymal lung diseases (DPLDs) of known origin”, group 12.03 “Sarcoidosis and other granulomatous ILDs/DPLDs” and group 12.04 “Rare ILDs/DPLDs”. The presented studies brought cutting-edge developments on several aspects of these conditions, incl

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