Gastrointestinal lymphoproliferative disorders

被引:20
作者
Banks, P. M.
机构
[1] Carolinas Med Ctr, Dept Pathol, Charlotte, NC 28203 USA
[2] Univ N Carolina, Chapel Hill, NC USA
关键词
diagnosis; gastrointestinal; immunohistochemistry; lymphoma; lymphoproliferative; MALT;
D O I
10.1111/j.1365-2559.2006.02571.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Malignant lymphomas can be first detected in some patients in endoscopic biopsies of the gastrointestinal (GI) tract. However, their recognition and accurate classification often pose problems for the pathologist for several reasons. First, the small sampling size limits pattern recognition and the number of ancillary studies which can be performed. Second, the immune system of the GI tract is capable of intense hyperplastic responses which may mimic lymphoma. Third, in a fashion similar to cutaneous lesions, those in the alimentary tract may be visualized and biopsied at a very early phase in their development when differentiation into neoplasia may be incomplete. Some forms of immune response actually pass through a poorly defined transition into lymphoma. Examples of such 'dysplasia' of the gut immune system include Helicobacter gastritis, coeliac disease and multicentric lymphoid hyperplasia associated with underlying immunodeficiency. With ever increasing endoscopic scrutiny of the gut by gastroenterologists, it is not surprising that the frequency of these indeterminate cases seems to be growing. In combination with careful clinical correlation and conventional microscopic analysis, selective immunohistochemical studies currently constitute the most powerful ancillary method in the pathologist's effort to recognize and classify GI lymphomas accurately.
引用
收藏
页码:42 / 54
页数:13
相关论文
共 48 条
  • [1] Mantle cell lymphoma: A clinicopathologic study of 80 cases
    Argatoff, LH
    Connors, JM
    Klasa, RJ
    Horsman, DE
    Gascoyne, RD
    [J]. BLOOD, 1997, 89 (06) : 2067 - 2078
  • [2] AZAB MB, 1989, CANCER-AM CANCER SOC, V64, P1208, DOI 10.1002/1097-0142(19890915)64:6<1208::AID-CNCR2820640608>3.0.CO
  • [3] 2-Z
  • [4] Mucosal intra-epithelial lymphocytes in enteropathy-associated T-cell lymphoma, ulcerative jejunitis, and refractory celiac disease constitute a neoplastic population
    Bagdi, E
    Diss, TC
    Munson, P
    Isaacson, PG
    [J]. BLOOD, 1999, 94 (01) : 260 - 264
  • [5] MANTLE CELL LYMPHOMA - A PROPOSAL FOR UNIFICATION OF MORPHOLOGICAL, IMMUNOLOGICAL, AND MOLECULAR-DATA
    BANKS, PM
    CHAN, J
    CLEARY, ML
    DELSOL, G
    DEWOLFPEETERS, C
    GATTER, K
    GROGAN, TM
    HARRIS, NL
    ISAACSON, PG
    JAFFE, ES
    MASON, D
    PILERI, S
    RALFKIAER, E
    STEIN, H
    WARNKE, RA
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1992, 16 (07) : 637 - 640
  • [6] BIENENSTOCK J, 1987, ANN ALLERGY, V59, P17
  • [7] The Burkitt-like lymphomas: a Southwest Oncology Group study delineating phenotypic, genotypic, and clinical features
    Braziel, RM
    Arber, DA
    Slovak, ML
    Gulley, ML
    Spier, C
    Kjeldsberg, C
    Unger, J
    Miller, TP
    Tubbs, R
    Leith, C
    Fisher, RI
    Grogan, TM
    [J]. BLOOD, 2001, 97 (12) : 3713 - 3720
  • [8] Ki67 staining pattern as a diagnostic tool in the evaluation of lymphoproliferative disorders
    Bryant, RJ
    Banks, PM
    O'Malley, DP
    [J]. HISTOPATHOLOGY, 2006, 48 (05) : 505 - 515
  • [9] Abnormal intestinal intraepithelial lymphocytes in refractory sprue
    Cellier, C
    Patey, N
    Mauvieux, L
    Jabri, B
    Delabesse, E
    Cervoni, JP
    Burtin, ML
    Guy-Grand, D
    Bouhnik, Y
    Modigliani, R
    Barbier, JP
    Macintyre, E
    Brousse, N
    Cerf-Bensussan, N
    [J]. GASTROENTEROLOGY, 1998, 114 (03) : 471 - 481
  • [10] Chadburn A, 1997, SEMIN DIAGN PATHOL, V14, P15