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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
|
pubmed:dateCreated |
1998-1-13
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pubmed:abstractText |
Lymphangioleiomyomatosis (LAM) is a rare disease which afflicts young women of childbearing age. Recently, it has been listed as an indication for lung transplantation. We describe a case of recurrent LAM in a 31-year-old woman occurring in the allograft of a male donor after single lung transplantation. Nonisotopic in situ hybridization shows that the smooth muscle cell proliferation is of donor origin.
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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 |
Dec
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pubmed:issn |
0046-8177
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
28
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1420-3
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pubmed:dateRevised |
2005-11-17
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pubmed:meshHeading |
pubmed-meshheading:9416700-Adult,
pubmed-meshheading:9416700-Cell Division,
pubmed-meshheading:9416700-Female,
pubmed-meshheading:9416700-Humans,
pubmed-meshheading:9416700-Lung Transplantation,
pubmed-meshheading:9416700-Lymphangioleiomyomatosis,
pubmed-meshheading:9416700-Muscle, Smooth,
pubmed-meshheading:9416700-Postoperative Complications,
pubmed-meshheading:9416700-Pulmonary Alveoli,
pubmed-meshheading:9416700-Recurrence
|
pubmed:year |
1997
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pubmed:articleTitle |
Lymphangioleiomyomatosis: recurrence after single lung transplantation.
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pubmed:affiliation |
Pathological Institute, Department of Surgery, Klinikum Grosshadern, University of Munich, Germany.
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pubmed:publicationType |
Journal Article,
Case Reports
|