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tracheobronchomegaly

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Also known as Mounier-Kuhn syndrome, Mounier-Kühn syndrome, Idiopathic tracheobronchomegaly, Congenital tracheobronchomegaly

Tracheobronchomegaly is a rare lung condition characterised by abnormal widening of the trachea and main bronchi, typically presenting with no symptoms, or a long-standing cough or recurrent chest infections. There may be copious purulent sputum production, eventually leading to bronchiectasis and other respiratory complications.

In the Vinony graph

Vinony's link graph records 18 inbound references to tracheobronchomegaly, and connects out to trachea, bronchus and respiratory tract.

It sits within the topics Bronchus disorders, Congenital disorders of respiratory system and Rare diseases.

Vinony links it to 6 Wikipedia language editions.

Research

343 papers

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Wikidata facts

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ICD-9-CM
748.3
NCI Thesaurus ID
C85196
health specialty
pulmonology
Sources (1)

via Wikidata · CC0

~2 min read

Encyclopedic overview

5 sections
Contents
  • Signs and symptoms
  • Diagnosis
  • History
  • References
  • External links

Tracheobronchomegaly is a rare lung condition characterised by abnormal widening of the trachea and main bronchi, typically presenting with no symptoms, or a long-standing cough or recurrent chest infections. There may be copious purulent sputum production, eventually leading to bronchiectasis and other respiratory complications.

It may be acquired secondary to another lung disease or medical lung procedure, but when no cause is identified it is presumed congenital and is known as Mounier-Kühn syndrome.

Excerpted from Wikipedia’s “tracheobronchomegaly” article, available under the CC BY-SA 4.0 licence.

Available in 6 languages

via Wikidata sitelinks · CC0

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