Source:http://linkedlifedata.com/resource/pubmed/id/11956788
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2-3
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pubmed:dateCreated |
2002-4-16
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pubmed:abstractText |
We report the rare case of an 11-year-old boy who presented with intractable hypoxaemia and a pulmonary mass. Investigations revealed this to be a pulmonary arteriovenous malformation. It was entirely confined to the right middle lobe and was successfully treated via a right middle lobectomy. The relevant literature with respect to both diagnosis and treatment is reviewed.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0179-0358
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
168-70
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:11956788-Arteriovenous Malformations,
pubmed-meshheading:11956788-Child,
pubmed-meshheading:11956788-Humans,
pubmed-meshheading:11956788-Male,
pubmed-meshheading:11956788-Pulmonary Artery,
pubmed-meshheading:11956788-Pulmonary Veins,
pubmed-meshheading:11956788-Tomography, X-Ray Computed
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pubmed:year |
2002
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pubmed:articleTitle |
Congenital pulmonary arteriovenous malformations.
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pubmed:affiliation |
Department of Surgery, Sydney Children's Hospital, Randwick, NSW, Australia.
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pubmed:publicationType |
Journal Article,
Case Reports
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