Academic literature on the topic 'Emphyseme pulmonaire lobaire'

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Journal articles on the topic "Emphyseme pulmonaire lobaire"

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Absher, Dale R., Vesna Martich Kriss, and Carol M. Cottrill. "Lobar emphysema due to anomalous aortic origin of the left pulmonary artery." Cardiology in the Young 9, no. 3 (May 1999): 327–30. http://dx.doi.org/10.1017/s1047951100005035.

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AbstractThe unusual case of an infant with aortic origin of the left pulmonary artery is presented. The patient developed a rare complication of lobar emphysema due to bronchial compression from the enlarged right pulmonary artery. Operative anastomosis of the left pulmonary artery to the pulmonary trunk was successful, with subsequent resolution of the lobar emphysema.
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Gonçalves, Carlos Alberto, Valdemar Martins, António Ochoa, and Pedro Carvalho. "PULMONARY LOBAR INTERSTITIAL EMPHYSEMA." Fetal and Pediatric Pathology 28, no. 4 (January 2009): 192–97. http://dx.doi.org/10.1080/15513810902984160.

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Berlinger, Norman T., Dennis P. Porto, and Theodore R. Thompson. "Infantile Lobar Emphysema." Annals of Otology, Rhinology & Laryngology 96, no. 1 (January 1987): 106–11. http://dx.doi.org/10.1177/000348948709600124.

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Infantile lobar emphysema is a symptom complex representing a spectrum of diseases characterized by overdistention of a pulmonary lobe by a check valve mechanism. The earlier in life infantile lobar emphysema presents, the more severe are the symptoms. Half of the cases appear in the first 4 weeks of life. The chest radiograph is the best diagnostic tool but can be misinterpreted. Computed tomography sometimes discloses the cause, which appears to be bronchial obstruction in 25% of cases. The bronchial obstruction may be due to intrinsic defects or to extrinsic compression. Bronchoscopy should be performed only in certain cases and then only with careful anesthetic management.
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Glüer, Sylvia, Marc Reismann, and Benno M. Ure. "Congenital Lobar Emphysema." Annals of Thoracic Surgery 85, no. 2 (February 2008): 665. http://dx.doi.org/10.1016/j.athoracsur.2007.06.021.

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Rajan, R. S., and OP Yadava. "Congenital lobar emphysema." Indian Journal of Thoracic and Cardiovascular Surgery 4, no. 1 (January 1985): 89–91. http://dx.doi.org/10.1007/bf02664097.

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Regier, Penny J., Aitor Gallastegui, and William F. Craft. "Successful Treatment of Congenital Lobar Emphysema in Multiple Lung Lobes in an English Bulldog Puppy." Journal of the American Animal Hospital Association 57, no. 2 (January 15, 2021): 96–100. http://dx.doi.org/10.5326/jaaha-ms-7088.

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ABSTRACT A 5 mo old male intact English bulldog was evaluated at a veterinary referral hospital for acute respiratory distress and chronic difficulty breathing. Thoracic radiographs revealed multifocal pulmonary hyperinflation and hyperlucency suspected in the left caudal and accessory lung lobes. A thoracic computed tomography scan identified severe diffuse enlargement of the caudal subsegment of the left cranial lung lobe and the dorsal process of the accessory lung lobe, with parenchymal hypoattenuation, rounded margins, and thin pulmonary vessels. Based on clinical signs and imaging findings, he was diagnosed with suspect congenital lobar emphysema in multiple lung lobes. A median sternotomy was performed, which revealed a hyperinflated, emphysematous left cranial lung lobe (caudal subsegment) and accessory lung lobe for which two lung lobectomies were performed. The remaining lung lobes were small and atelectatic. Histopathology revealed bronchial cartilage hypoplasia and aplasia and findings consistent with congenital lobar emphysema. The puppy recovered well from surgical treatment of congenital lobar emphysema, requiring multiple lung lobectomies, with subsequent computed tomography–evidenced re-expansion of the remaining lung lobes 3 mo after surgery. The patient is still alive 1 yr after surgery with a normal activity level and no evidence of respiratory compromise.
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Theilig, Dorothea, Ralf-Harto Huebner, Konrad Neumann, Alexander Poellinger, and Felix Doellinger. "Selecting Patients for Lobar Lung Volume Reduction Therapy: What Quantitative Computed Tomography Parameters Matter?" RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren 191, no. 01 (October 11, 2018): 40–47. http://dx.doi.org/10.1055/a-0638-0058.

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Purpose Evaluation of emphysema distribution with quantitative computed tomography (qCT) prior to endoscopic lung volume reduction (ELVR) is recommended. The aim of this study was to determine which of the commonly assessed qCT parameters prior to endoscopic lung volume reduction (ELVR) best predicts outcome of treatment. Materials and Methods 50 patients who underwent technically successful ELVR at our institution were retrospectively analyzed. We performed quantitative analysis of the CT scans obtained prior to ELVR and carried out Mann-Whitney U-tests and a logistic regression analysis to identify the qCT parameters that predict successful outcome of ELVR in terms of improved forced expiratory volume in 1 second (FEV1). Results In the Mann-Whitney U-test, the interlobar emphysema heterogeneity index (p = 0.008) and the pulmonary emphysema score (p = 0.022) showed a statistically significant difference between responders and non-responders. In multiple logistic regression analysis only the interlobar emphysema heterogeneity index (p = 0.008) showed a statistically significant impact on the outcome of ELVR, while targeted lobe volume, total lung volume, targeted lobe emphysema score and total lung emphysema score did not. Conclusion Of all commonly assessed quantitative CT parameters, only the heterogeneity index definitely allows prediction of ELVR outcome in patients with advanced chronic obstructive pulmonary disease (COPD). Key Points Citation Format
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Walsh, Timothy Andrew, Krishna Revanna Gopagondanahalli, and Atul Malhotra. "Williams-Beuren Syndrome and Congenital Lobar Emphysema: Uncommon Association with Common Pathology?" Case Reports in Pediatrics 2017 (2017): 1–4. http://dx.doi.org/10.1155/2017/3480980.

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Introduction. Congenital lobar emphysema (CLE) and Williams-Beuren Syndrome are two rare conditions that have only been reported together in a single case study. Case Presentation. We report another case of a male Caucasian newborn with nonspecific initial respiratory distress, with detection of CLE on repeat chest X-ray on Day 25 of life and concurrent ventricular septal defect, supravalvular aortic stenosis, and branch pulmonary stenosis, in whom a 7q11.23 deletion consistent with Williams-Beuren Syndrome was made. Conclusion. A diagnosis of congenital lobar emphysema should prompt further screening for congenital heart disease and genetic deletion, and further research is needed to investigate the role of elastin gene mutation in the development of the neonatal lung.
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Al Alaiyan, Saleh, Abdulhakiem Katan, and Omar Galal. "Infantile Lobar Emphysema and Absent Pulmonary Valve Syndrome." Annals of Saudi Medicine 16, no. 4 (July 1996): 444–46. http://dx.doi.org/10.5144/0256-4947.1996.444.

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Mirza, Bilal, AfsheenBatool Raza, Iftikhar Ijaz, Lubna Ijaz, Farah Naz, and Afzal Sheikh. "Intralobar pulmonary sequestration masquerading as congenital lobar emphysema." Journal of Indian Association of Pediatric Surgeons 16, no. 1 (2011): 15. http://dx.doi.org/10.4103/0971-9261.74515.

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Dissertations / Theses on the topic "Emphyseme pulmonaire lobaire"

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Verna, Dominique. "Emphysème lobaire congénital : à propos de deux cas." Montpellier 1, 1993. http://www.theses.fr/1993MON11063.

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Book chapters on the topic "Emphyseme pulmonaire lobaire"

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Yudkowitz, Francine S. "Congenital Pulmonary Cystic Lesions/Lobar Emphysema." In Essence of Anesthesia Practice, 91. Elsevier, 2011. http://dx.doi.org/10.1016/b978-1-4377-1720-4.00081-9.

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Finkle, Joshua H. "Pediatric Pulmonary Radiology." In Ultrasound Guided Procedures and Radiologic Imaging for Pediatric Anesthesiologists, edited by Anna Clebone, Joshua H. Finkle, and Barbara K. Burian, 107–20. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780190081416.003.0011.

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Chapter 11 examines radiologic images for common and uncommon pediatric pulmonary disorders. These include neonatal problems such as meconium aspiration, transient tachypnea of the newborn, respiratory distress syndrome, pulmonary interstitial emphysema, bronchopulmonary dysplasia, persistent pulmonary hypertension, neonatal pneumonia, and congenital diaphragmatic hernia. The chapter goes on to look at congenital lung anomalies such as congenital lobar overinflation, bronchopulmonary sequestration, and congenital pulmonary airway malformation. The lung tumor pleuropulmonary blastoma is described. Infections reviewed include pneumonia and viral bronchiolitis, and genetic disorders examined include acute chest syndrome, cystic fibrosis, and primary ciliary dyskinesia. The chapter covers the clinical features and anatomy associated with these disorders as well as their diagnosis based on the radiologic imaging.
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Conference papers on the topic "Emphyseme pulmonaire lobaire"

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Hilvers, Pamela, Mark Polak, Patrick Bacaj, and Robert A. Gustafson. "Coexistence Of Congenital Lobar Emphysema And Pulmonary Interstitial Glycogenosis In A Neonate." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a6737.

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Tsuzuku, Akifumi, Fumihiro Asano, Teruomi Miyazawa, Hiroshi Handa, Masamichi Mineshita, Yoshihiko Matusno, Takuya Sobajima, Atsunori Masuda, Anri Murakami, and Tomoya Kato. "CT assessment of lobar heterogenity and fissure integrity in pulmonary emphysema for bronchoscopic lung volume reduction with valve." In Annual Congress 2015. European Respiratory Society, 2015. http://dx.doi.org/10.1183/13993003.congress-2015.pa763.

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Argula, Rahul G., Charlie Strange, and Viswanathan Ramakrishnan. "The Degree Of Target Lobe Destruction Does Not Impact The Effect Of Lobar Perfusion On Exercise Response To Endobronchial Valve Therapy In Advanced Pulmonary Emphysema." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a2906.

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