rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
3
|
pubmed:dateCreated |
2002-8-2
|
pubmed:abstractText |
A 73-year-old woman with idiopathic pulmonary fibrosis (IPF) had an elevated serum CA19-9 level, but not KL-6. Her condition worsened and she subsequently died and this was associated with a rise in the serum KL-6 level. At autopsy, the lung showed a honeycomb appearance macroscopically and, microscopically, hyaline membrane formation was seen. Immunohistochemical staining revealed partial colocalization of KL-6 and CA19-9 to dilated bronchiolar cells. These features suggest that the mechanisms that cause the synthesis and release of CA19-9 and KL-6 from damaged lung tissue in IPF are likely to differ from those in diffuse alveolar damage. In addition, serum KL-6 levels may reflect the severity of disease more sensitively than CA19-9 levels.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
1323-7799
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
7
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
281-4
|
pubmed:dateRevised |
2008-11-21
|
pubmed:meshHeading |
pubmed-meshheading:12153695-Aged,
pubmed-meshheading:12153695-Antigens,
pubmed-meshheading:12153695-Antigens, Neoplasm,
pubmed-meshheading:12153695-Biological Markers,
pubmed-meshheading:12153695-Bronchi,
pubmed-meshheading:12153695-CA-19-9 Antigen,
pubmed-meshheading:12153695-Female,
pubmed-meshheading:12153695-Glycoproteins,
pubmed-meshheading:12153695-Humans,
pubmed-meshheading:12153695-Immunohistochemistry,
pubmed-meshheading:12153695-Mucin-1,
pubmed-meshheading:12153695-Mucins,
pubmed-meshheading:12153695-Pulmonary Alveoli,
pubmed-meshheading:12153695-Pulmonary Fibrosis,
pubmed-meshheading:12153695-Respiratory Mucosa,
pubmed-meshheading:12153695-Tissue Distribution
|
pubmed:year |
2002
|
pubmed:articleTitle |
Colocalization of CA19-9 and KL-6 to epithelial cells in dilated bronchioles in a patient with idiopathic pulmonary fibrosis complicated by diffuse alveolar damage.
|
pubmed:affiliation |
Department of Internal Medicine, Nanokaichi Municipal Hospital, Tomioka, Gunma, Japan. yshimizu@med.gunma-u.ac.jp
|
pubmed:publicationType |
Journal Article,
Case Reports
|