Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
795
pubmed:dateCreated
1992-5-11
pubmed:abstractText
Hilar and mediastinal lymphadenopathy associated with localized pulmonary amyloid is very rare. We describe two cases of this unusual combination, one of endobronchial amyloid with adenopathy and the other of nodular parenchymal amyloid with hilar nodes. In both these cases the nodes contained calcification, and in the nodular parenchymal case in particular, this appearance is highly suggestive of pulmonary amyloid.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/1561191-13030209, http://linkedlifedata.com/resource/pubmed/commentcorrection/1561191-13092776, http://linkedlifedata.com/resource/pubmed/commentcorrection/1561191-14213182, http://linkedlifedata.com/resource/pubmed/commentcorrection/1561191-2137018, http://linkedlifedata.com/resource/pubmed/commentcorrection/1561191-4811003, http://linkedlifedata.com/resource/pubmed/commentcorrection/1561191-5548752, http://linkedlifedata.com/resource/pubmed/commentcorrection/1561191-6344311, http://linkedlifedata.com/resource/pubmed/commentcorrection/1561191-6724579, http://linkedlifedata.com/resource/pubmed/commentcorrection/1561191-6857574, http://linkedlifedata.com/resource/pubmed/commentcorrection/1561191-707881, http://linkedlifedata.com/resource/pubmed/commentcorrection/1561191-869631, http://linkedlifedata.com/resource/pubmed/commentcorrection/1561191-891285, http://linkedlifedata.com/resource/pubmed/commentcorrection/1561191-935475
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0032-5473
pubmed:author
pubmed:issnType
Print
pubmed:volume
68
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
47-50
pubmed:dateRevised
2010-9-7
pubmed:meshHeading
pubmed:year
1992
pubmed:articleTitle
Organ limited amyloidosis with lymphadenopathy.
pubmed:affiliation
Department of Medicine, St George's Hospital, London, UK.
pubmed:publicationType
Journal Article, Case Reports