Zobrazeno 1 - 10
of 1 115
pro vyhledávání: '"lobar emphysema"'
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 108, Iss , Pp 102848- (2024)
Introduction: Congenital lobar emphysema (CLE) is a condition characterized by overinflation of one or more pulmonary lobes due to air-trapping, which can cause severe compression of adjacent structures. Bilateral CLE is rare but can cause severe res
Externí odkaz:
https://doaj.org/article/93813f75dd8545dc81fa003a132c8259
Publikováno v:
Journal of the Pakistan Medical Association, Vol 74, Iss 4 (2024)
This case report discusses the diagnostic challenge of congenital lobar emphysema (CLE) in a three-month old infant with severe respiratory distress. The infant was initially misdiagnosed and managed as a case of pneumothorax. This case highlights th
Externí odkaz:
https://doaj.org/article/8391491c09b049d89d9337fdfecd2026
Autor:
Syed Mohsin Aijaz, Gowhar Nazir Mufti, Waseem Jan Shah, Akshat Sudhanshu, Nisar Ahmad Bhat, Aejaz Ahsan Baba, Raashid Hamid, Sheikh Khurshid Ahmed
Publikováno v:
Journal of Pediatric Research, Vol 10, Iss 2, Pp 113-117 (2023)
Aim:A variety of developmental abnormalities of the tracheobronchial tree and pulmonary parenchyma are found in the newborn. There is limited data available on their presentation and clinical course from third world countries.Materials and Methods:A
Externí odkaz:
https://doaj.org/article/f2b9982398ab4d3584f9dc9d2d9fc9ab
Publikováno v:
Archives of Anesthesia and Critical Care, Vol 10, Iss 3 (2023)
Externí odkaz:
https://doaj.org/article/7a257723e4a3426eaeba584fdcd1ae7f
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 80, Iss 4 (2023)
Background: Congenital pulmonary malformations (CPMs) are rare in children. This study aimed to describe the clinical, imaging characteristics, and treatment of patients with this pathology. Methods: We conducted a descriptive and retrospective study
Externí odkaz:
https://doaj.org/article/528e28cec84a4215acfb92485de41a4c
Publikováno v:
Annals of Pediatric Surgery, Vol 18, Iss 1, Pp 1-8 (2022)
Abstract Background Bilateral congenital lobar emphysema is an extremely rare condition, and detailed workup of these patients is very important. Operative intervention is usually based on radiological, biochemical, and clinical details. Bronchoscopy
Externí odkaz:
https://doaj.org/article/7474933f2b824d81bb400a6835ff19ca
Autor:
Abenezer Zinaye, MD, Abrehet Zeray, MD
Publikováno v:
Radiology Case Reports, Vol 17, Iss 10, Pp 3481-3484 (2022)
Congenital lobar overinflation (CLO) is a rare congenital pulmonary abnormality characterized by progressive overexpansion of a lobe(s) exerting mass effect on the remaining lobes and the mediastinum. Bilateral involvement is extremely rare and has b
Externí odkaz:
https://doaj.org/article/e798f07221c748438fa37bc30f86de48
Publikováno v:
Frontiers in Veterinary Science, Vol 10 (2023)
An 11-week-old, sexually intact female Catahoula Leopard dog was evaluated for a multiple-week history of exercise intolerance and intermittent periods of respiratory distress. Thoracic radiographs revealed a markedly hyperinflated right lung field,
Externí odkaz:
https://doaj.org/article/55d821cd94e44045bdb33c8e844399dd
Autor:
Alba Ganarin, Valentina Agnese Ferraro, Alessandra Rancan, Silvia Carraro, Stefania Zanconato, Piergiorgio Gamba
Publikováno v:
Journal of Pediatric Surgery Open, Vol 1, Iss , Pp 100008- (2023)
Aim of the study: To evaluate clinical outcome and respiratory function in patients with congenital lobar/segmental emphysema (CLE/CSE) treated conservatively. Methods: In this single-centre retrospective study we included patients ≥5-year-old with
Externí odkaz:
https://doaj.org/article/61db864ade944c238efaf81bac13dead
Publikováno v:
Respiratory Medicine Case Reports, Vol 43, Iss , Pp 101842- (2023)
Congenital lobar emphysema (CLE) is caused by airway defects resulting in air trapping and hyperinflation of the affected lobe. Case reports of families affected with CLE imply a genetic etiology. However, the genetic contributions have not been well
Externí odkaz:
https://doaj.org/article/e7f12a2588e943a6bc848cc83264fc55