pubmed-article:10408351 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10408351 | lifeskim:mentions | umls-concept:C0007634 | lld:lifeskim |
pubmed-article:10408351 | lifeskim:mentions | umls-concept:C1744681 | lld:lifeskim |
pubmed-article:10408351 | lifeskim:mentions | umls-concept:C0205248 | lld:lifeskim |
pubmed-article:10408351 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:10408351 | pubmed:dateCreated | 1999-9-23 | lld:pubmed |
pubmed-article:10408351 | 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. | lld:pubmed |
pubmed-article:10408351 | pubmed:language | eng | lld:pubmed |
pubmed-article:10408351 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10408351 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:10408351 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10408351 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10408351 | pubmed:month | May | lld:pubmed |
pubmed-article:10408351 | pubmed:issn | 0303-6987 | lld:pubmed |
pubmed-article:10408351 | pubmed:author | pubmed-author:HucGG | lld:pubmed |
pubmed-article:10408351 | pubmed:author | pubmed-author:KARP KPK | lld:pubmed |
pubmed-article:10408351 | pubmed:author | pubmed-author:LeaM SMS | lld:pubmed |
pubmed-article:10408351 | pubmed:author | pubmed-author:ChoiJ HJH | lld:pubmed |
pubmed-article:10408351 | pubmed:author | pubmed-author:ChangS ESE | lld:pubmed |
pubmed-article:10408351 | pubmed:author | pubmed-author:CoxR KRK | lld:pubmed |
pubmed-article:10408351 | pubmed:author | pubmed-author:ShwayderTT | lld:pubmed |
pubmed-article:10408351 | pubmed:author | pubmed-author:MoonK CKC | lld:pubmed |
pubmed-article:10408351 | pubmed:author | pubmed-author:SungK JKJ | lld:pubmed |
pubmed-article:10408351 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:10408351 | pubmed:volume | 26 | lld:pubmed |
pubmed-article:10408351 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10408351 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10408351 | pubmed:pagination | 253-8 | lld:pubmed |
pubmed-article:10408351 | pubmed:dateRevised | 2004-11-17 | lld:pubmed |
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pubmed-article:10408351 | pubmed:year | 1999 | lld:pubmed |
pubmed-article:10408351 | pubmed:articleTitle | Congenital CD34-positive granular cell dendrocytosis. | lld:pubmed |
pubmed-article:10408351 | pubmed:affiliation | Department of Dermatology, Asan Medical Center, College of Medicine, University of Ulsan, Seoul, Korea. | lld:pubmed |
pubmed-article:10408351 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:10408351 | pubmed:publicationType | Case Reports | lld:pubmed |