Source:http://linkedlifedata.com/resource/pubmed/id/17638655
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
2007-7-19
|
pubmed:abstractText |
The categorization of pigmented purpuric dermatosis (PPD) as a form of cutaneous lymphoid dyscrasia has been suggested. Phenotypic and molecular studies were done on 43 patients with PPD. The molecular studies used a capillary gel electrophoresis T-cell receptor beta multiplex polymerase chain reaction assay. There were 2 principal categories: polyclonal PPD represented by 22 cases and monoclonal variants comprising 21 cases. Monoclonal cases had extensive skin lesions. An identical restricted T-cell repertoire independent of time and location was observed. Approximately 40% of the monoclonal cases had clinical and pathologic features of mycosis fungoides (MF). In the polyclonal variant, disease outside the lower extremities was uncommon; there were no patients with MF. Striking reductions in CD7 and CD62L were seen in both groups. PPD is a form of cutaneous T-cell lymphoid dyscrasia, based on the frequency of monoclonality, the preservation of persistent T-cell clonotypes, and extent of pan-T-cell marker loss. Stratification of lesions of PPD according to the molecular profile may be of significant value prognostically and influence therapeutic intervention.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0002-9173
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
128
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
218-29
|
pubmed:meshHeading |
pubmed-meshheading:17638655-Adolescent,
pubmed-meshheading:17638655-Adult,
pubmed-meshheading:17638655-Aged,
pubmed-meshheading:17638655-Aged, 80 and over,
pubmed-meshheading:17638655-Antigens, CD7,
pubmed-meshheading:17638655-Child,
pubmed-meshheading:17638655-Child, Preschool,
pubmed-meshheading:17638655-Female,
pubmed-meshheading:17638655-Humans,
pubmed-meshheading:17638655-Immunophenotyping,
pubmed-meshheading:17638655-L-Selectin,
pubmed-meshheading:17638655-Male,
pubmed-meshheading:17638655-Middle Aged,
pubmed-meshheading:17638655-Pigmentation Disorders,
pubmed-meshheading:17638655-Purpura
|
pubmed:year |
2007
|
pubmed:articleTitle |
Pigmented purpuric dermatosis: classification by phenotypic and molecular profiles.
|
pubmed:affiliation |
Department of Pathology and Laboratory Medicine, Weill Medical College of Cornell University New York Presbyterian Hospital-Cornell Campus, New York, NY 10021, USA.
|
pubmed:publicationType |
Journal Article
|