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 +5 more sources
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 ...
Deborah Babirye +2 more
exaly +4 more sources
Airway management for a patient with tracheobronchomegaly undergoing lobectomy: a case report [PDF]
BMC Anesthesiology, 2023 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 +3 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
Airway Management of Patient With Mounier–Kuhn Syndrome: A Case Report [PDF]
Respirology Case ReportsMounier–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
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
Fatiha Bounoua +2 more
exaly +4 more sources
An Unusual Cause of Spontaneous Pneumomediastinum: The Mounier-Kuhn Syndrome [PDF]
Case Reports in Pulmonology, 2019 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
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
Mounier-Kuhn Syndrome in an Elderly Female with Pulmonary Fibrosis [PDF]
Case Reports in Medicine, 2016 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 +3 more sources
Difficulties in the Differential Diagnosis of Tracheobronchomegaly in Children
Вестник рентгенологии и радиологии, 2020 Tracheobronchomegaly is a rare developmental defect in children, which is characterized by the expansion of the trachea and large bronchi, the diagnosis and treatment of which are made more often in adult practice, when the clinical diagnostic picture ...
N. A. Il’ina +3 more
doaj +3 more sources