Tracheobronchomegaly (Mounier-Kuhn Syndrome) in a 43-Year-Old Male: A Case Report [PDF]
Deborah Babirye,1 Jonathan Walubembe,1 Juliet Allen Babirye,2 Joseph Baruch Baluku,2,3 Pauline Byakika-Kibwika,4 Eva Nabawanuka1 1Department of Radiology, Makerere University College of Health Sciences, Kampala, Uganda; 2Department of Research, Makerere ...
Joseph Baruch Baluku +2 more
exaly +4 more sources
Unexpected curious cause of serious air leakage after endotracheal intubation: A case report of tracheobronchomegaly and literature review [PDF]
PurposeTracheobronchomegaly (TBM) is a rare disease with enlarged trachea and mainstem bronchi, which might not be diagnosed preoperatively because of patient’s nonsymptoms or clinicians’ overlook.
Jun Xiong +4 more
exaly +4 more sources
Airway Management of Patient With Mounier–Kuhn Syndrome: A Case Report [PDF]
Mounier–Kuhn syndrome (MKS) is a rare disorder characterised by tracheobronchomegaly, which poses significant anaesthetic challenges due to air leaks during mechanical ventilation.
Ali Karami +2 more
doaj +3 more sources
Mounier-Kuhn syndrome (Tracheobronchomegaly): Radiological diagnosis [PDF]
Mounier Kuhn Syndrome or tracheobronchomegaly is a rare disease, characterized by dilatation of the trachea and the main bronchi. Our study concerns a case of 67-years old male patient, smoker, with a chronic cough.
M. Rjimati, Resident +4 more
exaly +4 more sources
Tracheobronchomegaly: a case series and review of the literature [PDF]
BackgroundTracheobronchomegaly (TBM) is a rare condition characterized by abnormal dilation of the trachea and main bronchi owing to a pathological arrangement of smooth muscle fibers.
Zhenhua Li +6 more
exaly +4 more sources
Tracheobronchomegaly (Mounier-Kuhn Syndrome) with CT and bronchoscopic correlation: A case report [PDF]
Tracheobronchomegaly, or Mounier-Kuhn syndrome, is a clinical and radiological entity characterized by marked dilatation of the trachea and bronchi as a result of severe atrophy of the elastic fibers, with thinning of the muscularis, and the formation of
Hicham Naji-Amrani +2 more
exaly +4 more sources
Tracheobronchomegaly (Mounier-Kuhn syndrome) and Bronchiectasis as rare manifestations of Homocystinuria [PDF]
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
exaly +4 more sources
An Unusual Cause of Spontaneous Pneumomediastinum: The Mounier-Kuhn Syndrome [PDF]
Mounier-Kuhn syndrome is a rare clinical and radiologic condition. It is characterized by tracheal and bronchial dilation. Diagnosis is made by computed tomography and bronchoscopy.
Salim Naciri +3 more
doaj +3 more sources
Case Report: A case of reversible tracheal diameter Mounier-Kuhn syndrome and literature review [PDF]
Mounier-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 +2 more sources
A rare cause of dyspnea: Mounier Kuhn syndrome [PDF]
Mounier-Kuhn syndrome, also known as tracheobronchomegaly, is a rare clinical and radiological condition characterized by tracheobronchial dilatation and recurrent respiratory infections.
Feryal El Oualladi, MD +6 more
doaj +2 more sources

