Chan J K
Department of Pathology, Queen Elizabeth Hospital, Hong Kong.
Semin Diagn Pathol. 1996 Nov;13(4):260-96.
The first section of this article summarizes the salient clinicopathologic features of the more common types of primary gastrointestinal lymphomas, the recent explosion of information on the low grade B-cell lymphoma of mucosa-associated lymphoid tissue (MALT), and new findings on multiple lymphomatous polyposis and ulcerative jejunitis. The second section discusses the practical problems that may be encountered in the diagnosis of gastrointestinal lymphomas, including diagnosis of large cell malignancies, distinction between lymphoma and reactive lymphoid hyperplasia, classification of diffuse small B-cell lymphomas (including the potential pitfall of mistaking Burkitt's lymphoma for small B-cell lymphoma), recognition of large cell transformation in low-grade B-cell MALT lymphoma, assessment of gastric biopsies from MALT lymphoma patients after anti-Helicobacter therapy, and assessment of nodal or splenic involvement in low-grade MALT lymphoma.
本文第一部分总结了较常见的原发性胃肠道淋巴瘤的显著临床病理特征、黏膜相关淋巴组织(MALT)低度B细胞淋巴瘤方面近期激增的信息,以及多灶性淋巴瘤样息肉病和溃疡性空肠炎的新发现。第二部分讨论了胃肠道淋巴瘤诊断中可能遇到的实际问题,包括大细胞恶性肿瘤的诊断、淋巴瘤与反应性淋巴样增生的鉴别、弥漫性小B细胞淋巴瘤的分类(包括将伯基特淋巴瘤误诊为小B细胞淋巴瘤的潜在陷阱)、低度B细胞MALT淋巴瘤中高细胞转化的识别、抗幽门螺杆菌治疗后MALT淋巴瘤患者胃活检的评估,以及低度MALT淋巴瘤中淋巴结或脾脏受累情况的评估。