Results 91 to 100 of about 3,727 (171)
Causas congênitas de bronquiectasias não fibrocísticas: um relato de caso [PDF]
Dentre as causas congênitas de bronquiectasias podemos citar a Síndrome de Mounier-Kuhn, caracterizada pela presença de traqueobronquiomegalia associada, a qual teve cerca de 400 casos descritos em todo o mundo até o ano de 2021; bem como a Síndrome de ...
Acosta , Andrea Marcia Cunha +2 more
core +2 more sources
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
core
Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia, 2007 Mounier-Kuhn syndrome, or tracheobronchomegaly, is a rare clinical entity characterized by abnormal dilation of the trachea and main bronchi. The diagnosis can usually be made by measuring the tracheal diameter. We report the case of a 40-year-old black man with refractory lower respiratory tract infection.
Fabrício Piccoli, Fortuna +3 more
openaire +1 more source
TRACHEOBRONCHOMEGALY: A RARE CAUSE OF BILATERAL BRONCHIECTASIS
National 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
[Tracheobronchomegaly (Mounier-Kuhn syndrome].
Pneumonologia i alergologia polska, 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 ...
Agnieszka, Gawlewicz-Mroczka +2 more
openaire +3 more sources
Tracheobronchomegaly(Mounier-Kuhn Syndrome): a case report.
QJM : monthly journal of the Association of Physicians, 2023 Z. -. Li, R. Wang, Shan Gao
semanticscholar +1 more source
Imaging in non-cystic fibrosis bronchiectasis and current limitations [PDF]
, 2021 Balbi, Maurizio
core +1 more source
The Formyl Peptide Receptor 2 Regulates Microglial Phenotype Through Immunometabolism: Implications for Alzheimer’s Disease [PDF]
, 2019 Microglia are key players in the pathology of Alzheimer’s disease (AD), driving chronic inflammation, oxidative stress, and the altered metabolism seen in the brains of patients.
Wickstead, E., Wickstead, E.
core
A case of tracheobronchomegaly misdiagnosed as COPD: case report and literature review
BMC Pulmonary MedicineBackground Tracheobronchomegaly, also known as Mounier-Kuhn syndrome (MKS), is a rare congenital condition characterized by significant dilation of the trachea and main bronchi along with an abnormal wall structure.
Sai Yuan, Weiran Li, Mao Hua
doaj +1 more source