Results 71 to 80 of about 471 (156)
Mounier Kuhn syndrome in adult: a case report [PDF]
, 2017 Mounier-Kuhn syndrome or tracheobronchomegaly is a rare congenital abnormality of the trachea and main bronchi characterized by marked cystic dilatation of the tracheobronchial tree, associated with tracheal diverticulosis, bronchiectasis and recurrent ...
Deka, Nabanita +2 more
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Rare lung diseases ― should we pay more attention? [PDF]
, 2017 Rare diseases are defined as the diseases that affect less than one person in 2000 people [...
Radzikowska, Elżbieta
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A Morphometric study of human adult trachea and left main stem bronchus and its clinical implication [PDF]
, 2017 A morphometric study of human adult trachea and left main bronchus was undertaken in the Institute of Anatomy, Madras Medical College, Chennai - 3, on 40 embalmed cadavers of which 21 were male and 19 were female which are voluntarily donated to the ...
Srinivasan, V
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Tracheal diverticulum - A case report
Journal of Marine Medical Society, 2015 Tracheal diverticulum is a rare entity usually detected post-mortem. It may be congenital or acquired. Clinically the patient may be asymptomatic or present with chronic cough, dyspnea, stridor, repeated tracheobronchitis.
Rahul Tyagi, R S Negi
doaj +1 more source
Traqueobroncomegalia (Síndrome de Mournier-Kuhn) en una mujer de 75 años: reporte de un caso [PDF]
Tracheobronchomegaly, or Mounier-Kuhn syndrome, is a little-known disease characterized by dilation of the trachea and main bronchi, associated with recurrent respiratory infections, bronchiectasis, tracheomalacia, and tracheal diverticula.
Aparicio, Madonna, Carrasco, Nicolás
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Modern imaging of the tracheo-bronchial tree [PDF]
, 2010 Recent state-of-the-art computed tomography and improved three-dimensional (3-D) postprocessing techniques have revolutionized the capability of visualizing airway pathology, offering physicians an advanced view of pathology and allowing for appropriate ...
Laroia, Archana T +3 more
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Tracheobronchomegaly with Bronchomalacia
Korean Journal of Medicine, 2012 Tracheobronchomegaly, or Mounier-Kuhn syndrome, is a rare clinical and radiologic condition characterized by marked tracheobronchial dilatation and recurrent lower respiratory tract infections. It is thought to be due to a congenital anomaly. A diagnosis is typically made using computed tomography (CT) and bronchoscopy.
Jun Hee Lee +6 more
openaire +1 more source
A rare cause of recurrent respiratory infections [PDF]
, 2015 Universitatea de Stat de Medicină și Farmacie „Nicolae Testemiţanu”, Departamentul de medicină internă, Disciplina pneumologie și alergologie, Chișinău, Republica Moldova; Centrul de Diagnostic German, Chișinău, Republica ...
Botnaru, Victor +2 more
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A point of care neutrophil elastase activity assay identifies bronchiectasis severity, airway infection and risk of exacerbation [PDF]
, 2019 Introduction: Neutrophil elastase activity in sputum can identify patients at high risk of airway infection and exacerbations in bronchiectasis. Application of this biomarker in clinical practice is limited, because no point-of-care test is available. We
Aliberti, Stefano +13 more
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Early manifestation of ARDS in COVID-19 infection in a 51- year-old man affected by Mounier-Kuhn syndrome [PDF]
, 2020 A 51-year-old man known to be affected by Mounier-Kuhn syndrome (MKS). presented to Accident & Emergecy (A&E) with fever, dyspnea and deterioration of his chronic coughs.
Cegolon, L. +7 more
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