Source:http://linkedlifedata.com/resource/pubmed/id/10408351
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1999-9-23
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pubmed:abstractText |
Granular cell tumors involving the skin are mostly acquired lesions. The Schwann cell origin of these lesions is supported by positive immunostaining for S-100 protein and myelin basic protein. S-100- granular cell lesions rarely have been described in association with fibrous papules or dermatofibromas. The congenital variety of S-100- granular cell tumors occurs almost exclusively in the gingiva. The cell origin of these lesions is not well delineated. We report a hitherto undescribed case of a congenital cutaneous lesion which is histologically characterized by diffuse dermal infiltrates of S-100- but CD34+ granular dermal dendrocytes. The granular appearance of these CD34+ dendrocytes is attributed to an abundance of phagolysosomes. The pathogenetic mechanism of this unusual lesion remains to be elucidated.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0303-6987
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
26
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
253-8
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:10408351-Antigens, CD34,
pubmed-meshheading:10408351-Biopsy,
pubmed-meshheading:10408351-Cytoplasmic Granules,
pubmed-meshheading:10408351-Dendritic Cells,
pubmed-meshheading:10408351-Granular Cell Tumor,
pubmed-meshheading:10408351-Humans,
pubmed-meshheading:10408351-Immunohistochemistry,
pubmed-meshheading:10408351-Infant,
pubmed-meshheading:10408351-Male,
pubmed-meshheading:10408351-Microscopy, Electron,
pubmed-meshheading:10408351-Phagosomes,
pubmed-meshheading:10408351-Skin Neoplasms
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pubmed:year |
1999
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pubmed:articleTitle |
Congenital CD34-positive granular cell dendrocytosis.
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pubmed:affiliation |
Department of Dermatology, Asan Medical Center, College of Medicine, University of Ulsan, Seoul, Korea.
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pubmed:publicationType |
Journal Article,
Case Reports
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