Results 51 to 60 of about 311 (135)

Endotracheal Tube Dislodgment in a High-Risk Pulmonary Hypertensive Patient due to Undiagnosed Tracheomegaly: A Case Report

open access: yesGraduate Medical Education Research Journal, 2021
Introduction: Airway enlargement was first described histologically in 1872, but it was not clinically reported until 1932, when Dr. Mounier-Kuhn published his seminal radiographic studies.
Andrew Peck   +4 more
doaj   +1 more source

Mounier–Kuhn syndrome: a case of tracheal smooth muscle remodeling

open access: yesClinical Case Reports, Volume 5, Issue 2, Page 93-96, February 2017., 2017
Mounier–Kuhn syndrome is a rare clinical disorder characterized by tracheobronchial dilation and recurrent lower respiratory tract infections. While the etiology of the disease remains unknown, histopathological analysis of Mounier–Kuhn airways demonstrates that the disease is, in part, characterized by cellular changes in airway smooth muscle.
Daniel P. Cook   +7 more
wiley   +1 more source

A Case of Tracheo-Bronchomegaly Section in a Young Male [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2020
Tracheobronchomegaly (TBM) or Mounier-Kuhn syndrome is a disorder characterised by dilatation of trachea and major bronchi with tracheal diverticula leading to bronchiectasis as a complication.
Priti Meshram   +3 more
doaj   +1 more source

Severe Tracheobronchomalacia after Prolonged Intubation of Multitrauma Patient

open access: yesCase Reports in Surgery, Volume 2011, Issue 1, 2011., 2011
Tracheobronchomalacia is a condition with significant morbidity with many etiologies including iatrogenic ones and should be considered in critically ill ventilated trauma patients. We present a case of a multitrauma patient who had difficulty weaning from the ventilator after prolonged intubation followed by tracheostomy tube placement.
V. G. Sams   +6 more
wiley   +1 more source

Bronchus Cardiacus Accessorius Dexter

open access: yesDiagnostic and Therapeutic Endoscopy, Volume 5, Issue 3, Page 211-217, 1999., 1998
The diagnosis of bronchus cardiacus accessorius dexter (BCAD) has occurred in 25 cases during the bronchoscopic investigations of 30,000 adult patients of the authors. In most of the cases, this bronchial anomaly has been revealed as an accessory phenomenon, nevertheless, in one of the patients, it was the source of a considerable hemorrhage.
P. Barzó, B. Nagy
wiley   +1 more source

Complex Genomic Rearrangement Involving the TBX4 Promoter Manifesting With Variable Expressivity in a Five‐Generation Family

open access: yesHuman Mutation, Volume 2026, Issue 1, 2026.
Variants involving TBX4 are associated with ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension (ICPPS; also known as small patella syndrome), pulmonary arterial hypertension (PAH), and lethal lung developmental disorders.
Shruti A. Pande   +11 more
wiley   +1 more source

Case report: Mounier-Kuhn syndrome

open access: yesIndian Journal of Radiology and Imaging, 2008
Tracheobronchomegaly or Mounier-Kuhn syndrome is a rare disorder characterized by marked dilatation of the trachea and main bronchi, bronchiectasis, and recurrent respiratory tract infections.
Satish Kachhawa   +3 more
doaj   +1 more source

TRACHEOBRONCHOMEGALY: A RARE CAUSE OF BILATERAL BRONCHIECTASIS

open access: yesNational Journal of Medical Research, 2015
Mounier-Kuhn syndrome, also called tracheobronchomegaly, is a very rare congenital disorder of the lung primarily characterized by an abnormal widening of the upper airways.
Babaji Ghewade   +3 more
doaj  

Recurrent Lower Respiratory Tract Infection in a Renal Allograft Recipient: A Rare Case of Tracheobronchomegaly (Mounier-Kuhn Syndrome)

open access: yesIndian Journal of Transplantation
Mounier-Kuhn syndrome (MKS), also known as tracheobronchomegaly (TBM), is a rare disorder characterized by marked dilatation of the trachea and proximal bronchi. We hereby present a case of MKS in a 40-year-old renal transplant recipient. He had multiple
Monideep Saha   +5 more
doaj   +1 more source

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