Results 61 to 70 of about 471 (156)

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

A case of tracheobronchomegaly [PDF]

open access: yesEuropean Journal of Internal Medicine, 2017
Tracheobronchomegaly (Mounier-Kuhn syndrome) is a rare condition characterized by an abnormally enlarged trachea and main bronchi. Herein, we present a case of 79-year-old male with idiopathic pulmonary fibrosis and acute hypoxemic respiratory failure due to multilobar pneumonia. Computed tomography of the chest demonstrated a markedly dilated trachea,
Jirat Chenbhanich   +2 more
openaire   +2 more sources

Case report : Williams-Campbell syndrome [PDF]

open access: yes, 2009
Background: Williams-Campbell syndrome is a rare type of bronchiectasis that is due to deficiency or absence of cartilage in the fourth- to sixth-order bronchi.
Bestry, Iwona   +3 more
core  

Mounier-Kuhn syndrome : more than just a cough [PDF]

open access: yes, 2014
A 35-year-old man presented with a chronic productive cough and a history of recurrent lower respiratory tract infections. Physical examination was unremarkable as were routine blood investigations. A chest radiograph demonstrated dilation of the trachea
Attard, Joseph   +3 more
core   +1 more source

THE RARE CASE OF MONIER KUHN SYNDROME OR THE TRACHEOBRONCHOMEGALY SYNDROME [PDF]

open access: yes, 2015
Tracheobronchomegaly is a rare disease and is essentially characterized by moderate to severe dilatation of the trachea as well as segments of the bronchial tree. The result is recurrent infections.
Hassan, Ashfaq Ul   +3 more
core   +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

Mounier-Kuhn Syndrome [PDF]

open access: yes, 2015
Background: A 38-year-old male with no medical history complains about hemoptysis, chest pain, dyspnea on exertion and a cough. He has a history of occasional smoking, but had quitted smoking 1 year previously.
E. Schiettecatte   +3 more
core   +2 more sources

Tracheobronchomegaly: The Mounier-Kuhn syndrome [PDF]

open access: yes, 2018
A case of tracheobronchomegaly (Mounier-Kuhn syndrome) is reported. The striking features are gross dilatation of the trachea and both main bronchi with associated chronic pulmonary disease.
Bass, E.M.
core   +2 more sources

Anesthesia for a patient with unexpected giant tracheobronchomegaly

open access: yesTzu Chi Medical Journal, 2017
Tracheobronchomegaly (also called Mounier–Kuhn syndrome) is a rare disease characterized by flaccid and markedly dilated trachea and main bronchi on inspiration with narrowing or collapse on expiration or cough.
Chien-Ching Lee   +3 more
doaj   +1 more source

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