Tracheobronchomegaly (Mounier-Kuhn Syndrome) in a 43-Year-Old Male: A Case Report [PDF]
International Medical Case Reports Journal, 2022 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
Mounier-Kuhn syndrome (Tracheobronchomegaly): Radiological diagnosis [PDF]
Radiology Case Reports, 2021 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]
Frontiers in MedicineBackgroundTracheobronchomegaly (TBM) is a rare condition characterized by abnormal dilation of the trachea and main bronchi owing to a pathological arrangement of smooth muscle fibers.
Rujuan Wang
exaly +4 more sources
Tracheobronchomegaly (Mounier-Kuhn Syndrome) with CT and bronchoscopic correlation: A case report [PDF]
Radiology Case Reports, 2022 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, Fatiha Bounoua
exaly +4 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
exaly +4 more sources
Congenital tracheobronchomegaly (Mounier-Kuhn syndrome) in a 70-year-old nonsmoking male: A rare presentation in a low-resource setting [PDF]
Respiratory Medicine Case ReportsBackground: Mounier-Kuhn Syndrome (MKS), or congenital tracheobronchomegaly, is a rare disorder characterized by dilation of the trachea and main bronchi due to the atrophy of elastic and smooth muscle fibers.
Eiman Aboaziza
exaly +4 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 +2 more sources
Unexpected curious cause of serious air leakage after endotracheal intubation: A case report of tracheobronchomegaly and literature review [PDF]
Frontiers in Surgery, 2022 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
doaj +2 more sources
A rare cause of dyspnea: Mounier Kuhn syndrome [PDF]
Radiology Case ReportsMounier-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
Tracheobronchomegaly associated with tracheobronchopathia osteochondroplastica: a case report [PDF]
Frontiers in MedicineTracheobronchomegaly (TBM) is a rare condition characterized by the dilatation of the trachea and bronchi due to severe atrophy of elastic fibers, accompanied by the thinning of the muscularis mucosae and the development of diverticula between ...
Zhen Hua Li +4 more
doaj +2 more sources