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pubmed-article:9269556pubmed:abstractTextAn unusual case of aggressive Stage IIE(B) primary natural killer cell lymphoma of the caecum is described in a 16-year old Chinese girl. The immunophenotype of the tumour cells was CD2+, CD3-, CD4-, CD5-, CD7+, CD8-, CD45RO+, CD45RA-, CD56+, CD57-. Southern blot analysis showed a normal germline arrangements of the T-cell antigen receptor and immuno-globulin heavy chain genes. This lymphoma pursued a highly aggressive clinical course, with the rapid development of an extensive local recurrence after an apparently complete resection and combination cytotoxic therapy. The patient died 7 months after diagnosis, despite receiving salvage treatment. Given the aggressiveness and poor prognosis in this biologically distinct primary gastrointestinal lymphoma, a more vigorous systemic therapy should be considered in addition to surgery.lld:pubmed
pubmed-article:9269556pubmed:languageenglld:pubmed
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pubmed-article:9269556pubmed:authorpubmed-author:CnenG DGDlld:pubmed
pubmed-article:9269556pubmed:authorpubmed-author:JohnsonP JPJlld:pubmed
pubmed-article:9269556pubmed:authorpubmed-author:LauK YKYlld:pubmed
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pubmed-article:9269556pubmed:volume9lld:pubmed
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pubmed-article:9269556pubmed:pagination191-4lld:pubmed
pubmed-article:9269556pubmed:dateRevised2008-3-10lld:pubmed
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pubmed-article:9269556pubmed:year1997lld:pubmed
pubmed-article:9269556pubmed:articleTitleAggressive primary natural killer cell lymphoma of the caecum: a case report and literature review.lld:pubmed
pubmed-article:9269556pubmed:affiliationChinese University of Hong Kong, Prince of Wales Hospital, Hong Kong.lld:pubmed
pubmed-article:9269556pubmed:publicationTypeJournal Articlelld:pubmed
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