Matches in SemOpenAlex for { <https://semopenalex.org/work/W4313568644> ?p ?o ?g. }
Showing items 1 to 84 of
84
with 100 items per page.
- W4313568644 endingPage "1036" @default.
- W4313568644 startingPage "1033" @default.
- W4313568644 abstract "Cystic fibrosis is an autosomal recessive genetic disorder that damages the exocrine function of the body, resulting in alterations of multiple organs. In the respiratory system, it is known to cause bronchiectasis, recurrent bronchitis, and pneumonia; however, to the best of our knowledge, there are no reported cases of pulmonary arteriovenous malformations associated with this disease. Herein, we report a case of cystic fibrosis with multiple pulmonary arteriovenous malformations. A 16-year-old girl, who has been monitored since childhood for pancreatitis of unknown cause, experienced respiratory symptoms and hypoxemia (PaO2 = 57 mmHg). At 13 years of age, chest computed tomography revealed bronchiectasis, bronchial wall thickening, and tree-in-bud sign. Genetic testing was performed, and the patient was diagnosed with cystic fibrosis. However, the computed tomography scan also showed incidental nodular lesions in the left superior and both the inferior pulmonary lobes, suggesting multiple arteriovenous malformations. Dynamic computed tomography was performed which, confirmed the presence of 3 pulmonary arteriovenous malformations. Coil embolization was performed on all lesions, and the hypoxemia was corrected. Marked hypoxemia in a patient with cystic fibrosis may not be explained only by the presence of bronchiectasis and/or bronchial wall thickening; in such cases, it may be necessary to examine possible additional findings on computed tomography images, such as arteriovenous malformations." @default.
- W4313568644 created "2023-01-06" @default.
- W4313568644 creator A5003686923 @default.
- W4313568644 creator A5030106411 @default.
- W4313568644 creator A5044575740 @default.
- W4313568644 creator A5066578960 @default.
- W4313568644 creator A5075314880 @default.
- W4313568644 creator A5078175026 @default.
- W4313568644 creator A5078928565 @default.
- W4313568644 creator A5078931094 @default.
- W4313568644 date "2023-03-01" @default.
- W4313568644 modified "2023-10-14" @default.
- W4313568644 title "Cystic fibrosis with multiple pulmonary arteriovenous malformations: A case report" @default.
- W4313568644 cites W1988047965 @default.
- W4313568644 cites W2009664680 @default.
- W4313568644 cites W2016388542 @default.
- W4313568644 cites W2025939137 @default.
- W4313568644 cites W2056755489 @default.
- W4313568644 cites W2087334060 @default.
- W4313568644 cites W2110158978 @default.
- W4313568644 cites W2117024255 @default.
- W4313568644 cites W2160984255 @default.
- W4313568644 cites W2163010779 @default.
- W4313568644 cites W2169487898 @default.
- W4313568644 cites W2171064960 @default.
- W4313568644 cites W4206008652 @default.
- W4313568644 cites W4241884576 @default.
- W4313568644 doi "https://doi.org/10.1016/j.radcr.2022.12.024" @default.
- W4313568644 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36684625" @default.
- W4313568644 hasPublicationYear "2023" @default.
- W4313568644 type Work @default.
- W4313568644 citedByCount "0" @default.
- W4313568644 crossrefType "journal-article" @default.
- W4313568644 hasAuthorship W4313568644A5003686923 @default.
- W4313568644 hasAuthorship W4313568644A5030106411 @default.
- W4313568644 hasAuthorship W4313568644A5044575740 @default.
- W4313568644 hasAuthorship W4313568644A5066578960 @default.
- W4313568644 hasAuthorship W4313568644A5075314880 @default.
- W4313568644 hasAuthorship W4313568644A5078175026 @default.
- W4313568644 hasAuthorship W4313568644A5078928565 @default.
- W4313568644 hasAuthorship W4313568644A5078931094 @default.
- W4313568644 hasBestOaLocation W43135686441 @default.
- W4313568644 hasConcept C126322002 @default.
- W4313568644 hasConcept C126838900 @default.
- W4313568644 hasConcept C142724271 @default.
- W4313568644 hasConcept C164705383 @default.
- W4313568644 hasConcept C2776779939 @default.
- W4313568644 hasConcept C2776938444 @default.
- W4313568644 hasConcept C2777714996 @default.
- W4313568644 hasConcept C2779379686 @default.
- W4313568644 hasConcept C71924100 @default.
- W4313568644 hasConcept C75603125 @default.
- W4313568644 hasConceptScore W4313568644C126322002 @default.
- W4313568644 hasConceptScore W4313568644C126838900 @default.
- W4313568644 hasConceptScore W4313568644C142724271 @default.
- W4313568644 hasConceptScore W4313568644C164705383 @default.
- W4313568644 hasConceptScore W4313568644C2776779939 @default.
- W4313568644 hasConceptScore W4313568644C2776938444 @default.
- W4313568644 hasConceptScore W4313568644C2777714996 @default.
- W4313568644 hasConceptScore W4313568644C2779379686 @default.
- W4313568644 hasConceptScore W4313568644C71924100 @default.
- W4313568644 hasConceptScore W4313568644C75603125 @default.
- W4313568644 hasIssue "3" @default.
- W4313568644 hasLocation W43135686441 @default.
- W4313568644 hasLocation W43135686442 @default.
- W4313568644 hasLocation W43135686443 @default.
- W4313568644 hasOpenAccess W4313568644 @default.
- W4313568644 hasPrimaryLocation W43135686441 @default.
- W4313568644 hasRelatedWork W1970639481 @default.
- W4313568644 hasRelatedWork W1989920528 @default.
- W4313568644 hasRelatedWork W2016807943 @default.
- W4313568644 hasRelatedWork W2052566619 @default.
- W4313568644 hasRelatedWork W2091042844 @default.
- W4313568644 hasRelatedWork W2120066589 @default.
- W4313568644 hasRelatedWork W2160654539 @default.
- W4313568644 hasRelatedWork W2340393060 @default.
- W4313568644 hasRelatedWork W2355557977 @default.
- W4313568644 hasRelatedWork W2982784367 @default.
- W4313568644 hasVolume "18" @default.
- W4313568644 isParatext "false" @default.
- W4313568644 isRetracted "false" @default.
- W4313568644 workType "article" @default.