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Perforation predicts poor prognosis in patients with primary intestinal diffuse large B-cell lymphoma.

AbstractAIMS:
To elucidate the clinicopathological features and prognostic factors of primary intestinal diffuse large B-cell lymphoma (PI-DLBL).
METHODS AND RESULTS:
Archival tissues from 30 tumours were used for tissue microarray construction, immunohistochemistry and interphase fluorescence in situ hybridization for chromosomal translocation. The M:F ratio was 1.7:1, with a median age of 60 years. The ileum and ileocaecum were most frequently involved (40% each). Fourteen (47%) were at stage I(E) disease, 15 (50%) at stage II(E). Five (17%) tumours were perforated at presentation. The tumours expressed Bcl-6 (73%), MUM1 (70%), Bcl-2 (67%) and CD10 (23%). Nine (30%) were classified as germinal centre B-cell (GCB) phenotype and 21 non-GCB. Eight of 30 (27%), 7/30 (23%) and 2/29 (7%) cases were positive for rearrangements involving IGH, BCL6, and C-MYC loci, respectively, whereas all cases were negative for BCL2 and CCND1 translocation. Perforation was a poor prognostic indicator, with a hazard ratio of tumour-related death at 8.75 (P = 0.001). The differentiation antigens, GCB versus non-GCB phenotype, or lymphoma-associated translocations were of no prognostic significance.
CONCLUSIONS:
We found a higher rate of perforation and lower frequency of GCB phenotype in PI-DLBL in Taiwan compared with other geographical areas; perforation is a poor prognostic indicator.
AuthorsS-S Chuang, H Ye, S-F Yang, W-T Huang, H-K Chen, P-P Hsieh, W-S Hwang, K-Y Chang, C-L Lu, M-Q Du
JournalHistopathology (Histopathology) Vol. 53 Issue 4 Pg. 432-40 (Oct 2008) ISSN: 1365-2559 [Electronic] England
PMID18983608 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Female
  • Germinal Center (pathology)
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization, Fluorescence
  • Intestinal Neoplasms (diagnosis, mortality, pathology)
  • Lymphoma, Large B-Cell, Diffuse (diagnosis, mortality, pathology)
  • Male
  • Middle Aged
  • Phenotype
  • Prognosis
  • Survival Analysis
  • Translocation, Genetic

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