Brooks J J, Enterline H T
Cancer. 1983 Feb 1;51(3):476-86. doi: 10.1002/1097-0142(19830201)51:3<476::aid-cncr2820510320>3.0.co;2-s.
Three separate histologic types of gastric pseudolymphoma (GPL) are described: (1) the common "inflammatory" type usually accompanied by ulceration and extensive fibrosis; (2) the entity known as "nodular lymphoid hyperplasia," which was associated with multiple intestinal lesions; and (3) the third reported case of angiofollicular lymphoid hyperplasia of the stomach (one with nodal involvement). Criteria for the common type were developed and, in general, confirm previous studies. However, the importance of evaluating nuclear cytology and mitotic rate are stressed. Organ infiltration by chronic lymphocytic leukemia should be excluded by the absence of an absolute peripheral lymphocytosis. In addition to the ten cases presented, the literature on 175 previous cases is summarized. GPL is estimated to account for 10-15% of all gastric lymphoid tumors. In comparison to gastric lymphoma, GPL is usually smaller in size and occurs a decade earlier on the average. Since an associated focal lymphoma was documented in an additional five cases, this study proposes that pseudolymphoma be considered a precursor lesion with malignant potential. Extensive pathologic sampling and total surgical excision are recommended.
本文描述了三种不同组织学类型的胃假性淋巴瘤(GPL):(1)常见的“炎症性”类型,通常伴有溃疡和广泛纤维化;(2)称为“结节性淋巴组织增生”的实体,与多个肠道病变相关;(3)第三例报道的胃血管滤泡性淋巴组织增生(一例有淋巴结受累)。制定了常见类型的标准,总体上证实了先前的研究。然而,强调了评估核细胞学和有丝分裂率的重要性。应通过无绝对外周淋巴细胞增多排除慢性淋巴细胞白血病的器官浸润。除了所呈现的10例病例外,还总结了先前175例病例的文献。GPL估计占所有胃淋巴瘤的10%-15%。与胃淋巴瘤相比,GPL通常体积较小,平均发病时间早十年。由于另外5例病例记录了相关的局灶性淋巴瘤,本研究提出假性淋巴瘤应被视为具有恶性潜能的前驱病变。建议进行广泛的病理取样和完整的手术切除。