Results 21 to 30 of about 1,257,115 (148)
A curious case of cough: Mounier-Kuhn syndrome in a Namibian female patient [PDF]
The Pan African Medical Journal, 2020 We report a case of a 43-year-old female who presented with a history of recurrent productive cough, since her teenage years. Her associated symptoms included dyspnoea, occasional pleuritic chest pain and rarely, constitutional symptoms. Treated numerous
Mercy Juliette Mkandawire +2 more
doaj +3 more sources
Huge Tracheal Diverticulum in a Patient with Mounier-Kuhn Syndrome [PDF]
European Journal of Case Reports in Internal Medicine, 2016 Tracheal diverticulum is a rare benign entity. Tracheobronchomegaly (TBM), also known as Mounier-Kuhn syndrome, is a rare disorder characterized by marked dilation of the trachea and main bronchi, associated with thinning or atrophy of the elastic tissue.
Michele Mondoni +4 more
doaj +4 more sources
[Mounier-Kuhn syndrome]. [PDF]
Aten Primaria, 2020 Mounier Kuhn syndrome or tracheobronchomegaly is characterized by a marked dilatation of the trachea and main bronchi that can extend to the periphery of the lungs.
Castro HM +3 more
europepmc +4 more sources
Mounier-Kuhn Syndrome Flare With Pleuritic Chest Pain: A Discussion of Complications and Management. [PDF]
Case Rep PulmonolBackground Mounier‐Kuhn syndrome (MKS), or tracheobronchomegaly, is a rare disorder characterized by dilation of the trachea and main bronchi due to atrophy of elastic and smooth muscle fibers. It is associated with recurrent respiratory infections, bronchiectasis, and airway collapse.
Maule G +5 more
europepmc +2 more sources
Journal of the Belgian Society of Radiology, 2015 Background: A 38-year-old male with no medical history complains about hemoptysis, chest pain, dyspnea on exertion and a cough. He has a history of occasional smoking, but had quitted smoking 1 year previously.
E. Schiettecatte +3 more
doaj +5 more sources
Síndrome de Mounier-Kühn Mounier-Kuhn syndrome [PDF]
Jornal Brasileiro de Pneumologia, 2006 A síndrome de Mounier-Kühn, ou traqueobroncomegalia congênita, é uma entidade clínica rara caracterizada pela dilatação anormal de traquéia e brônquios principais. O diagnóstico geralmente pode ser realizado através da mensuração do diâmetro traqueal. Os
Fabrício Piccoli Fortuna +3 more
doaj +2 more sources
Tracheobronchomegaly (Mounier-Kuhn syndrome) and Bronchiectasis as rare manifestations of Homocystinuria [PDF]
Respiratory Medicine Case Reports, 2023 Homocystinuria (HCU) is a rare autosomal recessive inherited disorder usually diagnosed in childhood. It is characterized by a deficiency of the enzyme that converts homocysteine to cystathionine.
Aasir M. Suliman +2 more
doaj +2 more sources
An atypical encounter: Mounir-Kuhn syndrome and aspergilloma coexistence: A case report
Radiology Case ReportsWe report a coexistence of Mounir-Kuhn syndrome and aspergilloma in a 69-year-old male presented with hemoptysis, cough, shortness of breath and fever.
Sima Babiker, MBBS +1 more
doaj +2 more sources
Tracheobronchomegaly as a Cause of Bronchiectasis in an Adult
Case Reports in Pulmonology, 2016 Mounier-Kuhn syndrome (MKS) is a rare congenital anomaly characterized by dilated trachea and main bronchi due to atrophy of the elastic fibers and smooth muscle cells of the trachea and major airways. Patients of MKS can have varied presentation.
Vishnukanth Govindaraj +3 more
doaj +2 more sources
Mounier-Kuhn syndrome - a case report of airway management during general anesthesia [PDF]
Respiratory Medicine Case ReportsIntroduction: Mounier-Kuhn syndrome (MKS) is a rare tracheobronchial disorder with fewer than 500 reported cases globally. This report describes an asymptomatic MKS patient diagnosed incidentally due to unexplained intraoperative airway leakage during ...
Weiwei Sun +3 more
doaj +2 more sources