Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2008-5-28
pubmed:abstractText
Primary cutaneous aggressive epidermotropic CD8+ cytotoxic T-cell lymphoma is a rare and provisional entity, characterised by cutaneous involvement and aggressive clinical behaviour. The case is here presented of a young woman with concurrent cutaneous and systemic involvement. Despite multi-agent chemotherapy, only partial remission could be achieved, and the patient died from therapy-resistant respiratory and circulatory failure. This case report is intended to add to the data collected on this rare entity, with only about 20 cases as yet described.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1472-4146
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
61
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
770-2
pubmed:meshHeading
pubmed-meshheading:18505891-Adult, pubmed-meshheading:18505891-Antigens, CD, pubmed-meshheading:18505891-Antineoplastic Combined Chemotherapy Protocols, pubmed-meshheading:18505891-Biological Markers, pubmed-meshheading:18505891-CD8-Positive T-Lymphocytes, pubmed-meshheading:18505891-Cyclophosphamide, pubmed-meshheading:18505891-Dexamethasone, pubmed-meshheading:18505891-Doxorubicin, pubmed-meshheading:18505891-Female, pubmed-meshheading:18505891-Gene Rearrangement, gamma-Chain T-Cell Antigen Receptor, pubmed-meshheading:18505891-Humans, pubmed-meshheading:18505891-Immunophenotyping, pubmed-meshheading:18505891-Karyotyping, pubmed-meshheading:18505891-Lymphoma, T-Cell, Cutaneous, pubmed-meshheading:18505891-Skin Neoplasms, pubmed-meshheading:18505891-Translocation, Genetic, pubmed-meshheading:18505891-Treatment Failure, pubmed-meshheading:18505891-Vincristine
pubmed:year
2008
pubmed:articleTitle
Rare provisional entity: primary cutaneous aggressive epidermotropic CD8+ cytotoxic T-cell lymphoma in a young woman.
pubmed:affiliation
1st Department of Pathology and Experimental Cancer Research, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
pubmed:publicationType
Journal Article, Case Reports