نتایج جستجو برای: congenital lobar emphysema

تعداد نتایج: 132278  

Journal: :The Journal of Thoracic and Cardiovascular Surgery 1961

Journal: :Thorax 2012
Helgo Magnussen Mordechai R Kramer Anne-Marie Kirsten Charles Marquette Arschang Valipour Franz Stanzel Reiner Bonnet Juergen Behr Oren Fruchter Yael Refaely Ralf Eberhardt Felix J F Herth

RATIONALE Interlobar fissure integrity has previously correlated with responsiveness to endobronchial lung volume reduction therapy in patients with advanced emphysema. OBJECTIVE This report summarises the effect of interlobar fissure integrity on responses to treatment with a novel endoscopic tissue sealant (AeriSeal emphysematous lung sealant (ELS)) that collapses hyperinflated lung. METH...

Journal: : 2022

Khí phế thũng thùy phổi bẩm sinh (Congenital Lobar Emphysema - SLE) được biết đến như là căng chướng quá mức sinh, đặc trưng bởi dấu hiệu tăng kích thước của phổi. Hầu hết các trường hợp biểu hiện ngay trong tháng đầu đời; triệu chứng suy hô hấp điển hình. Những nhẹ thường bị bỏ qua và bệnh có thể ở trẻ lớn hơn song hiếm. CLE liên quan với một phần hoặc toàn bộ quản bít tắc, hệ quả (a) khiếm kh...

Journal: :Annals of Thoracic and Cardiovascular Surgery 2014

Journal: :Journal of Veterinary Medical Science 1992

2017
Luis Prats-Sanchez Alejandro Martínez-Domeño Pol Camps-Renom Raquel Delgado-Mederos Daniel Guisado-Alonso Rebeca Marín Laura Dorado Salvatore Rudilosso Alejandra Gómez-González Francisco Purroy Manuel Gómez-Choco David Cánovas Dolores Cocho Moises Garces Sonia Abilleira Joan Martí-Fàbregas

BACKGROUND AND PURPOSE Remote parenchymal haemorrhage (rPH) after intravenous thrombolysis is defined as hemorrhages that appear in brain regions without visible ischemic damage, remote from the area of ischemia causing the initial stroke symptom. The pathophysiology of rPH is not clear and may be explained by different underlying mechanisms. We hypothesized that rPH may have different risk fac...

Journal: :The Eurasian journal of medicine 2009
Atila Turkyilmaz Yener Aydin Ali Fuat Erdem Atilla Eroglu Nurettin Karaoglanoglu

PURPOSE Congenital cystic pulmonary malformations (CPM) are rare anomalies. The purpose of this study was to present our experience with CPM patients who were surgically treated in our clinic and to discuss our findings along with those from the literature. MATERIALS AND METHODS Surgical treatment was performed on 19 patients under the age of 16 who were diagnosed with CPM in our clinic betwe...

2011
Eun Ah Jung Ji Hye Lee Hyun Deuk Cho Ki Hyun Seo Seock Yeol Lee Young Tong Kim

Development of the respiratory system begins at 3 weeks gestation, and aberrations in the developmental processes may give rise to a group of structural abnormalities collectively referred to as bronchopulmonary foregut malformations (BPFMs). The common BPFMs include congenital cystic adenomatoid malformation (CCAM), pulmonary sequestration, congenital lobar emphysema, and bronchogenic cysts (B...

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