Lewin K J, Ranchod M, Dorfman R F
Cancer. 1978 Aug;42(2):693-707. doi: 10.1002/1097-0142(197808)42:2<693::aid-cncr2820420241>3.0.co;2-j.
A study was made of 117 patients who presented with gastrointestinal lymphoma. The occurrence was 48 in the stomach, 37 in the small intestine, 13 in the ileocecal region, two in the appendix and 11 in the large intestine. In six cases, multiple sites in the gastrointestinal tract were involved, but in five cases this appeared to be secondary to massive mesenteric or retroperitoneal lymph node disease. Using Rappaport's classification, diffuse histiocytic lymphoma was the most frequent histologic type and constituted 60% of the cases. Nodular lymphomas comprised 10% of the total, nodular poorly differentiated lymphocytic lymphoma forming the majority of this group. Ten of the lymphomas were undifferentiated, 5 of Burkitt's type and 5 non-Burkitt's type. Five were Mediterranean-type lymphomas associated with plasma cell infiltration of the adjacent mucosa, and only two cases of primary Hodgkin's disease were encountered. Two lymphomas could not be classified. Eight percent of the cases showed plasmacytoid changes and were classified as a distinct subgroup of the parent lymphoma rather than as examples of extramedullary plasmacytoma. Gastrointestinally lymphomas occurred most frequently during the fourth to seventh decades. However, nine lymphomas occurred in children younger than 16 years of age. In comparison to adults, the childhood lymphomas showed a number of notable differences with respect to sex distribution, site of involvement and histologic type. Information concerning the extent of the disease at the time of diagnosis was available in 75 cases. Of these, 49% of the lymphomas were confined to the affected viscus and 33% had associated regional lymph node involvement; the remaining 18% had mode widespread disease. In 44 patients information on the spread of disease was available and in 48% there was extra abdominal spread. Prognosis appeared to correlate best with the stage of the disease rather than the histologic type.
对117例胃肠道淋巴瘤患者进行了研究。发病部位为胃48例,小肠37例,回盲部13例,阑尾2例,大肠11例。6例胃肠道有多个部位受累,但5例似乎是继发于大量肠系膜或腹膜后淋巴结病变。采用拉帕波特分类法,弥漫性组织细胞淋巴瘤是最常见的组织学类型,占病例的60%。结节性淋巴瘤占总数的10%,其中结节性低分化淋巴细胞淋巴瘤占该组的大多数。10例淋巴瘤为未分化型,5例为伯基特型,5例为非伯基特型。5例为地中海型淋巴瘤,伴有相邻黏膜的浆细胞浸润,仅遇到2例原发性霍奇金病。2例淋巴瘤无法分类。8%的病例出现浆细胞样改变,被归类为母淋巴瘤的一个独特亚组,而非髓外浆细胞瘤的例子。胃肠道淋巴瘤最常见于40至70岁之间。然而,9例淋巴瘤发生在16岁以下的儿童。与成人相比,儿童淋巴瘤在性别分布、受累部位和组织学类型方面存在一些显著差异。75例患者有诊断时疾病范围的信息。其中,49%的淋巴瘤局限于受累脏器,33%伴有区域淋巴结受累;其余18%有更广泛的疾病。44例患者有疾病扩散的信息,48%有腹外扩散。预后似乎与疾病分期的相关性最好,而非组织学类型。