Results 31 to 40 of about 471 (156)
Bronchiectasis with tracheobronchial dilation. [PDF]
Marchiori E, Hochhegger B, Zanetti G.
europepmc +3 more sources
Beyond Tuberculosis: A Rare Case of Mounier-Kuhn Syndrome in an Ethiopian Woman With Chronic Cough and Bronchiectasis. [PDF]
ABSTRACT This case highlights the importance of considering rare conditions like Mounier‐Kuhn Syndrome in patients with chronic respiratory symptoms, especially in regions with high tuberculosis prevalence. Enhanced awareness and advanced imaging are vital for accurate diagnosis and effective management of such conditions.
Deshimo G, Demeke E.
europepmc +2 more sources
Incidental finding or the incognito culprit? A case of Mounier-Kuhn syndrome. [PDF]
Key Clinical Message Mounier‐Kuhn syndrome, characterized by tracheal dilatation due to the loss of elastic fibers and smooth muscle cells, is a rare condition, often leading to recurrent respiratory infections from impaired mucociliary clearance.
Ozgur SS +5 more
europepmc +2 more sources
Tracheobronchomegaly, cough and recurrent chest infection: Mounier-Kuhn syndrome. [PDF]
Satia I +4 more
europepmc +2 more sources
Chronic rhinosinusitis and asthma commonly co‐occur, but no studies have leveraged the very large sample sizes needed to address whether preexisting CRS is associated with new onset asthma over time. In a longitudinal study of over 900,000 persons from 2008 to 2019, prevalent CRS (identified with sinus CT scan or diagnoses) was associated with 1.5‐ to ...
Brian S. Schwartz +9 more
wiley +1 more source
Anesthetic management of a patient with Mounier-Kuhn syndrome undergoing off-pump coronary artery bypass graft surgery -A case report- [PDF]
Mounier-Kuhn-syndrome patients have markedly dilated trachea and main bronchi due to an atrophy or absence of elastic fibers and thinning of smooth muscle layers in the tracheobronchial tree.
Jeong Jin Min +5 more
doaj +1 more source
We used mice that are haploinsufficient for Col5a1 (Col5a1+/−), a well‐accepted model of classical EDS type, and demonstrated the presence of primary changes in the lung parenchyma that are reminiscent of emphysema. We then performed a detailed analysis of the respiratory mechanics, lung volumes, and flow–volume curves and show that both male and ...
Jordan Fett +3 more
wiley +1 more source
Difficulties in the Differential Diagnosis of Tracheobronchomegaly in Children
Tracheobronchomegaly is a rare developmental defect in children, which is characterized by the expansion of the trachea and large bronchi, the diagnosis and treatment of which are made more often in adult practice, when the clinical diagnostic picture ...
N. A. Il’ina +3 more
doaj +1 more source
Anesthetic experience of a patient with tracheomegaly -A case report- [PDF]
Tracheomegaly or tracheobronchomegaly is a rare syndrome that consists of marked dilatation of the trachea and the major bronchi, and this is usually due to a congenital defect of the elastic and muscle fibers of the tracheobroncheal tree.
Mi Young Kim +5 more
doaj +1 more source
Background. Mounier-Kuhn syndrome or tracheobronchomegaly is a rare disorder characterized by marked dilatation of the trachea and main bronchi, bronchiectasis, and recurrent respiratory tract infections.
Pešut Dragica +4 more
doaj +1 more source

