PMID- 14657713 OWN - NLM STAT- MEDLINE DCOM- 20040105 LR - 20190823 IS - 0147-5185 (Print) IS - 0147-5185 (Linking) VI - 27 IP - 12 DP - 2003 Dec TI - Primary cutaneous diffuse large B-cell lymphoma: prognostic significance of clinicopathological subtypes. PG - 1538-45 AB - Classification and subdivision of primary cutaneous diffuse large B-cell lymphoma (PCDLBCL) are a matter of ongoing debate. In this study we assessed the morphologic, immunophenotypic, and clinical features of 30 cases of PCDLBCL identified during a review of all primary cutaneous B-cell lymphomas in the Scotland and Newcastle Lymphoma Group database. We also determined the number of cases harboring t(14;18) using a polymerase chain reaction and primers to the major breakpoint cluster region. The effect on prognosis of a variety of clinical and pathologic factors was assessed for the group of 30 PCDLBCL and the 5-year disease-specific survival (DSS) of this cohort compared with that of 195 cases of stage I diffuse large B-cell lymphoma arising primarily in lymph nodes, also identified from within the Scotland and Newcastle Lymphoma Group database. Location on the leg was the only independent prognostic factor for determining outcome in PCDLBCL (67% 5-year DSS compared with 100% for the upper body; P = 0.0047). The presence of multiple lesions, involvement of more than one body site, and expression or not of CD10, bcl-2, bcl-6, and CD10 and bcl-6, had no effect on survival. Compared with cases arising above the waist, those on the leg were more often female, were of an older age, and had a significantly higher incidence of bcl-2 expression (P = 0.002) as well as the aforementioned poorer prognosis. They also showed more frequent co-expression of CD10 and bcl-6, supporting a follicle center cell origin for some, but this difference was not statistically significant. Although there was no significant difference in the 5-year DSS between the group of PCDLBCL and the cases of stage I nodal diffuse large B-cell lymphoma (88% 5-year DSS vs. 78%; P = 0.06), the latter were generally treated with more aggressive therapy. Moreover, a significant difference in 5-year DSS was seen when the nodal DLBCLs were compared with PCDLBCLs arising above the waist (78% vs. 100% respectively; P = 0.0135). These results support the current EORTC approach of subdividing PCLBCL on the basis of site to produce prognostically relevant groupings. FAU - Goodlad, John R AU - Goodlad JR AD - Department of Pathology, Raigmore Hospital, Inverness, Scotland, United Kingdom. John.Goodlad@raigmore.scot.nhs.uk FAU - Krajewski, Andrew S AU - Krajewski AS FAU - Batstone, Paul J AU - Batstone PJ FAU - McKay, Pam AU - McKay P FAU - White, Jo M AU - White JM FAU - Benton, E Claire AU - Benton EC FAU - Kavanagh, Gina M AU - Kavanagh GM FAU - Lucraft, Helen H AU - Lucraft HH CN - Scotland and Newcastle Lymphoma Group LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Am J Surg Pathol JT - The American journal of surgical pathology JID - 7707904 RN - 0 (Biomarkers, Tumor) SB - IM MH - Adolescent MH - Adult MH - Age Factors MH - Aged MH - Aged, 80 and over MH - Biomarkers, Tumor/*metabolism MH - Female MH - Humans MH - Leg/pathology MH - Lymphoma, B-Cell/*mortality/*pathology/therapy MH - Lymphoma, Large B-Cell, Diffuse/*mortality/*pathology/therapy MH - Male MH - Middle Aged MH - Polymerase Chain Reaction MH - Prognosis MH - Sex Factors MH - Survival Analysis MH - Treatment Outcome MH - Upper Extremity/pathology EDAT- 2003/12/06 05:00 MHDA- 2004/01/06 05:00 CRDT- 2003/12/06 05:00 PHST- 2003/12/06 05:00 [pubmed] PHST- 2004/01/06 05:00 [medline] PHST- 2003/12/06 05:00 [entrez] AID - 10.1097/00000478-200312000-00006 [doi] PST - ppublish SO - Am J Surg Pathol. 2003 Dec;27(12):1538-45. doi: 10.1097/00000478-200312000-00006.