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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1987-5-27
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pubmed:abstractText |
Forty-two cases of lung cancer complicated with diffuse interstitial pulmonary fibrosis (DIPF) were selected from 13,056 autopsy cases. They were divided into primary (Group I and II) and secondary (Group III) DIPF, and histopathologic and clinicopathologic studies were made. The prevalence of lung cancer with primary DIPF was 17% (8/47) which was significantly (p less than 0.01) higher than that without DIPF (7% or 886/13,009). All eight cases of lung cancer in Group I and II were male, and 7 had cigarette-smoking history. The anatomical sites of lung cancer and DIPF were all peripheral in origin, and in 7 cases located primarily in the lower lobes (left:right = 6:1). Adenocarcinoma was the most common type. The study suggests that male DIPF patients with long clinical history should be followed thoroughly for lung cancer.
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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 |
Jan
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pubmed:issn |
0001-6632
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
37
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
11-9
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:3033984-Adenocarcinoma,
pubmed-meshheading:3033984-Aged,
pubmed-meshheading:3033984-Carcinoma, Small Cell,
pubmed-meshheading:3033984-Carcinoma, Squamous Cell,
pubmed-meshheading:3033984-Female,
pubmed-meshheading:3033984-Humans,
pubmed-meshheading:3033984-Lung Neoplasms,
pubmed-meshheading:3033984-Male,
pubmed-meshheading:3033984-Middle Aged,
pubmed-meshheading:3033984-Pulmonary Fibrosis,
pubmed-meshheading:3033984-Smoking
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pubmed:year |
1987
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pubmed:articleTitle |
Diffuse interstitial pulmonary fibrosis and lung cancer.
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pubmed:publicationType |
Journal Article
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