Results 81 to 90 of about 471 (156)
Revista Portuguesa de Pneumologia, 2007 A síndroma de Mounier-Kuhn é uma doença rara, de etiologia desconhecida e que se presume subdiagnosticada. Cursa frequentemente com infecções respiratórias de repetição e bronquiectasias. A clínica inespecífica, semelhante a outras patologias supurativas
Ana Marques +4 more
doaj
Diffuse bronchiectasis of genetic origin [PDF]
, 2014 Bronchiectasis is a significant cause of morbidity and mortality. It is the end point of a pathological process. We should be aiming to identify at risk patients before they develop bronchiectasis and treat them aggressively to prevent disease ...
Pike, KC
core
Etiology, clinical, radiological, and microbiological profile of patients with non-cystic fibrosis bronchiectasis at a tertiary care hospital of Pakistan [PDF]
, 2020 Objectives: To identify the etiology of non-cystic fibrosis bronchiectasis (NCFB), to assess the clinical presentation, radiological findings, and microbiological profile of patients presenting with a diagnosis of bronchiectasis in a tertiary care center
Baig, Mirza Saifullah +3 more
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Jornal Brasileiro de Pneumologia, 2008 O objetivo deste ensaio pictórico foi apresentar as principais alterações tomográficas observadas em doenças que acometem a traquéia de forma difusa.
Edson Marchiori +8 more
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A case report of bullous emphysema in an adolescent: congenitalmalformation or outcome of bronchopulmonary dysplasia? [PDF]
, 2021 Pulmonary emphysema belongs to the group of chronic obstructive pulmonary diseases, and inpediatric pulmonology is one of the complex diagnoses that require a careful differential diagnosis.
Fialkovska, Anastasiia +2 more
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Beyond recurrent infections: a rare case of Mounier-Kuhn syndrome with tracheobronchial dilatation
The Egyptian Journal of BronchologyMounier Kuhn syndrome (MKS), also known as tracheobronchomegaly (TBM), is a very rare and chronic airway disease characterized by marked dilatation of the trachea and central bronchi. Currently, there are few epidemiological studies on MKS, and most data
Mohsen Sadeghi +3 more
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William Campbell Syndrome as a Cause of Asymmetrical Bronchiectasis In a 10-Year-Old Child: A Case Report [PDF]
Background: William Campbell Syndrome is a rare congenital disease of the bronchial cartilages involving the 4th to 6th generation of bronchial divisions with involvement of bilateral lungs.
Asim Rehman +5 more
core +2 more sources
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
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Mounier-Kuhn syndrome (MKS) - Pathognomonic Findings [PDF]
Journal of Clinical and Diagnostic Research, 2014 Saurabh Kumar, Alok Kumar Mittal
doaj +1 more source
Tracheobronchomegaly: A rare but easily misdiagnosed disease
Asian Journal of Surgery, 2023 Shuhan Li, Liang Dong, Lili Zhi
doaj +1 more source