Results 41 to 50 of about 1,257,115 (148)
Prevalence of chronic respiratory diseases in Aboriginal children: A whole population study
Pediatric Pulmonology, Volume 57, Issue 12, Page 3136-3144, December 2022., 2022 Abstract Background The burden of bronchiectasis is disproportionately high in Aboriginal adults, with early mortality. Bronchiectasis precursors, that is, protracted bacterial bronchitis (PBB) and chronic suppurative lung disease (CSLD), often commence in early childhood.
Pamela Laird +18 more
wiley +1 more source
Mounier-Kuhn Syndrome- A Rare Case Report [PDF]
Journal of Clinical and Diagnostic Research, 2021 Mounier-Kuhn Syndrome (M-K Syndrome) also known as Tracheobronchomalacia (TBM) often seen in middle aged and elderly people. Weakness of the tracheal and bronchial walls allows the posterior and anterior walls to draw nearer together during expiration ...
YASH RANA +4 more
doaj +1 more source
Tracheobronchomegaly-Mounier-Kuhn syndrome
Saudi Medical Journal, 2004 Tracheobronchomegaly is a rare disorder of uncertain etiology, characterized by marked dilatation of the trachea and major bronchi, associated with tracheal diverticulosis, bronchiectasis and recurrent respiratory tract infection. We are reporting a 60-year-old man from the Kingdom of Saudi Arabia with this condition and review the literature for such ...
Hatem F, Al-Mubarak, Sabina A, Husain
openaire +4 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 +1 more source
Mounier-Kuhn syndrome: Case report and literature review [PDF]
, 2022 El síndrome de Mounier-Kuhn o traqueobroncomegalia es una condición rara caracterizada por dilatación de la tráquea y del árbol bronquial, la cual se produce por la reducción y atrofia de las fibras elásticas de la tráquea y los bronquios, por lo que ...
Villacrés, Fabián +4 more
core +1 more source
Mounier-Kuhn Syndrome Mimicking Lymphangioleiomyomatosis. [PDF]
Chest, 2018 We present the case of a man with Mounier-Kuhn syndrome (MKS), or tracheobronchomegaly, who was referred to the National Institutes of Health Clinical Research Center because of a potential diagnosis of lymphangioleiomyomatosis (LAM), a rare condition in men. The patient was evaluated using ongoing protocols and provided written informed consent.
Pacheco GG +5 more
europepmc +4 more sources
An unusual cause of recurrent spontaneous pneumothorax: the Mounier-Kuhn syndrome [PDF]
, 2016 Balbay, Ege Gulec/0000-0002-1557-7019; Annakkaya, Ali Nihat N/0000-0002-7661-8830;WOS: 000366159400049PubMed: 26127019We present a case of 63-year-old man who was referred to the emergency department with a right-sided pneumothorax.
Safçı, Sinem +6 more
core +1 more source
A Case of Tracheo-Bronchomegaly Section in a Young Male [PDF]
Journal 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
EHA2021 Virtual Congress Abstract Book
, 2021 HemaSphere, Volume 5, Issue S2, June 2021.
wiley +1 more source
Case Reports in Pulmonology, Volume 2014, Issue 1, 2014., 2014 Mounier‐Kuhn Syndrome (MKS) is a rare congenital disease that presents with abnormal enlargement in the central airways. In MKS, tracheomegaly is accompanied by difficulty in expelling recurrent lung infections and bronchiectasia. We presented a patient with MKS where commercially made stents were inadequate for stabilization and a custom‐made, self ...
Cengiz Özdemir +5 more
wiley +1 more source