CLASSIFICATION OF PRIMARY GASTRIC LYMPHOMAS ACCORDING TO HISTOLOGIC FEATURES

Citation
Ed. Hsi et al., CLASSIFICATION OF PRIMARY GASTRIC LYMPHOMAS ACCORDING TO HISTOLOGIC FEATURES, The American journal of surgical pathology, 22(1), 1998, pp. 17-27
Citations number
51
Categorie Soggetti
Pathology,Surgery
ISSN journal
01475185
Volume
22
Issue
1
Year of publication
1998
Pages
17 - 27
Database
ISI
SICI code
0147-5185(1998)22:1<17:COPGLA>2.0.ZU;2-W
Abstract
Histologic features of low-grade gastric lymphomas of mucosa-associate d lymphoid tissue (MALT) have been extensively described, and transfor mation to a large cell (high-grade) lymphoma can occur. We characteriz e high-grade gastric lymphoma histologically in an attempt to distingu ish between MALT-type and non-MALT-type lesions. We studied a series o f 60 gastric lymphomas and characterized them clinically, histopatholo gically, and immunophenotypically. Low-grade gastric lymphomas were cl assified according to established criteria. High-grade lymphomas were classified in three groups based on the presence or absence of a low-g rade component and lymphoepithelial lesions (LELs): 1) high-grade MALT lymphomas appearing in low-grade MALT lymphomas (LG/HG MALT lymphoma) ; 2) large cell lymphoma with LELs composed of large cells (high-grade LELs) but without a low-grade component (HG MALT lymphoma); and 3) di ffuse large cell lymphoma without a low-grade MALT lymphoma component or LELs (DLCL). Twenty-two lymphomas were classified as low-grade MALT lymphomas, 16 as LG/HG MALT lymphomas, 10 as HG MALT lymphomas, and 1 2 as DLCL. B-cell immunophenotype was confirmed in all 55 cases in whi ch immunophenotyping was performed. Low-grade LELs were seen in all lo w-grade MALT lymphomas, and CD20(L26) expression confirmed B-cell phen otype in the LELs in 20 of 20 cases. Clinical follow-up was available for 56 patients (range, 1-264 months; mean, 57 months). Actuarial anal ysis of disease-specific survival and relapse-free survival showed tha t clinical stage was highly statistically significant (P < 0.0001), wh ereas histologic type and grade approached statistical significance. M ultivariate analysis showed that clinical stage was the only significa nt factor in relapse-free and disease-specific survival.