Source:http://linkedlifedata.com/resource/pubmed/id/20724810
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2010-8-20
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pubmed:abstractText |
A 67-year-old man had undergone a right ureteronephrectomy because of a right ureter tumor, but the pathological diagnosis was inflammatory tissue with plasma cells, lymphocytes, and fibrosis. About 3 years later, abdominal computed tomography (CT) revealed a solid tumor at the left renal hilus. We resected the tumor and the pathological diagnosis was the same as before. More than 2 years later, because of elevated pancreatic enzymes, immunoglobulin G (IgG) and IgG4, more detailed examinations ware done, and he was diagnosed with IgG4-related autoimmune pancreatitis. We believe that the retroperitoneal tumor was retroperitoneal fibrosis associated with IgG4-related sclerosing disease. Now, he is being treated with steroid therapy. IgG4-related sclerosing disease is a systemic disease whose concept is now being established. Much more work is needed to understand this disease.
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pubmed:language |
jpn
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0018-1994
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
56
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
371-5
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pubmed:meshHeading |
pubmed-meshheading:20724810-Aged,
pubmed-meshheading:20724810-Autoimmune Diseases,
pubmed-meshheading:20724810-Diagnosis, Differential,
pubmed-meshheading:20724810-Humans,
pubmed-meshheading:20724810-Immunoglobulin G,
pubmed-meshheading:20724810-Male,
pubmed-meshheading:20724810-Pancreatitis,
pubmed-meshheading:20724810-Retroperitoneal Fibrosis,
pubmed-meshheading:20724810-Retroperitoneal Neoplasms,
pubmed-meshheading:20724810-Sclerosis
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pubmed:year |
2010
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pubmed:articleTitle |
[A case report of retroperitoneal fibrosis associated with IgG4-related sclerosing disease].
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pubmed:affiliation |
The Department of Urology, Osaka University Graduate School of Medicine, Osaka, Japan.
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pubmed:publicationType |
Journal Article,
English Abstract,
Review,
Case Reports
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