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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
|
pubmed:dateCreated |
1982-8-26
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pubmed:abstractText |
The clinical course of three patients with cutaneous T-cell lymphoma (CTCL) in whom skeletal disease developed is presented and the literature on skeletal involvement in these disorders is reviewed. Three separate types of skeletal manifestations occurred: (1) osteolytic lesions, (2) osteoblastic lesions, and (3) diffuse osteoporosis. Hypercalcemia was present in two cases. Tumor cells from two patients in short-term culture secreted osteoclast-activating factor(s). Both of these patients had pathologic evidence of osteoclast activation in bone sections. Thus, the tumor cells in certain patients with CTCL may derive from a monoclonal proliferation of a T-cell subset capable of producing humoral bone-resorbing factor(s) similar to those demonstrated in cultures of mitogen- and antigen-activated normal lymphocytes. Since skeletal lesions are unusual, it would follow that other T-cell subsets account for pathologic cell proliferation in most patients with CTCL.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
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pubmed:issn |
0003-987X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
118
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
461-7
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pubmed:dateRevised |
2008-3-17
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pubmed:meshHeading |
pubmed-meshheading:6979976-Adult,
pubmed-meshheading:6979976-Bone Resorption,
pubmed-meshheading:6979976-Female,
pubmed-meshheading:6979976-Humans,
pubmed-meshheading:6979976-Hypercalcemia,
pubmed-meshheading:6979976-Male,
pubmed-meshheading:6979976-Middle Aged,
pubmed-meshheading:6979976-Mycosis Fungoides,
pubmed-meshheading:6979976-Osteoporosis,
pubmed-meshheading:6979976-Osteosclerosis,
pubmed-meshheading:6979976-Sezary Syndrome,
pubmed-meshheading:6979976-Skin Neoplasms,
pubmed-meshheading:6979976-T-Lymphocytes
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pubmed:year |
1982
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pubmed:articleTitle |
Skeletal manifestations in cutaneous T-cell lymphomas.
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pubmed:publicationType |
Journal Article,
Case Reports
|