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
Tracheobronchomegaly associated with tracheobronchopathia osteochondroplastica: a case report [PDF]
Tracheobronchomegaly (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
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
Airway management for a patient with tracheobronchomegaly undergoing lobectomy: a case report [PDF]
Background Tracheobronchomegaly (TBM) is a rare disorder mainly characterized by dilatation and malacia of the trachea and major bronchi with diverticularization.
Sai-Nan Wang +4 more
doaj +2 more sources
Airway management of a patient with Mounier-Kuhn syndrome during general anesthesia - A case report - [PDF]
Background Mounier-Kuhn syndrome (MKS) is a rare disorder characterized by abnormal dilation of the trachea and main bronchi. MKS can be easily missed on chest X-rays, making diagnosis difficult.
Boreum Cheon +3 more
doaj +2 more sources
Mounier-Kuhn Syndrome in an Elderly Female with Pulmonary Fibrosis
Mounier-Kuhn syndrome (MKS), or tracheobronchomegaly, is a rare clinical and radiologic condition characterized by pronounced tracheobronchial dilation and recurrent lower respiratory tract infections.
Panagiotis Boglou +4 more
doaj +2 more sources
Congenital tracheobronchomegaly (Mounier-Kuhn syndrome) in a 70-year-old nonsmoking male: A rare presentation in a low-resource setting [PDF]
Background: 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.
Yousif Aboaziza +4 more
doaj +2 more sources
Tracheobronchomegaly as a Cause of Bronchiectasis in an Adult
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 variable course disease [PDF]
Mounier-Kuhn syndrome or tracheobronchomegaly is a rare disease characterized by marked dilation of the trachea and proximal bronchi with recurrent lower tract respiratory infections.
Lobna Loued +7 more
doaj +2 more sources
An atypical encounter: Mounir-Kuhn syndrome and aspergilloma coexistence: A case report [PDF]
We 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

