Results 31 to 40 of about 1,465 (136)
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 +4 more sources
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 +4 more sources
Flexible bronchoscopy and mechanical ventilation in managing Mounier-Kuhn syndrome: a case report [PDF]
São Paulo Medical Journal, 2017 CONTEXT: Mounier-Kuhn syndrome is a rare congenital condition with distinct dilatation and diverticulation of the tracheal wall. The symptoms may vary and the treatment usually consists of support.
Aslihan Gürün Kaya +3 more
doaj +5 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 +5 more sources
Case Report: A case of reversible tracheal diameter Mounier-Kuhn syndrome and literature review [PDF]
Frontiers in MedicineMounier-Kuhn syndrome (MKS), also known as tracheobronchomegaly (TBM) or tracheomegaly, is an extremely rare and chronic airway disease characterized by significant dilation of the trachea and central bronchi.
Lu-xia Kong, Zhen-hua Li, Ji-xiang Ni
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 +5 more sources
Mounier-Kuhn syndrome masquerading pulmonary thromboembolism in an elderly male [PDF]
Lung India, 2014 Mounier-Kuhn syndrome, also referred to as tracheobronchomegaly, is a rare idiopathic clinical and radiologic disorder characterized by significant tracheobronchial dilation.
Pankaj Gupta +3 more
doaj +3 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
An atypical encounter: Mounir-Kuhn syndrome and aspergilloma coexistence: A case report [PDF]
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