Lewin K J, Kahn L B, Novis B H
Cancer. 1976 Dec;38(6):2511-28. doi: 10.1002/1097-0142(197612)38:6<2511::aid-cncr2820380641>3.0.co;2-u.
The clinical and pathological features of 17 "Western" type primary abdominal lymphomas (WTL) are compared with 14 of "Mediterranean" type (MTL). The MTL involved only young adult Mulatto and African patients in whom malabsorption and abdominal pain were the major clinical features. The WTL also predominantly affected Mulatto patients but four cases occurred in Caucasians, and the mean age at presentation was two decades later. An obstructive presentation was the most common; only one patient in this group had evidence of malabsorption. The WTLs were located mainly in the distal small bowel and were nearly all of monomorphic lymphocytic or histiocytic type. The MTLs were sited mainly in the duodenum and jejunum and were of an unusual pleomorphic histologic type. A spectrum of cells from those resembling atypical lymphocytes to large histiocytic types were seen, some of the latter resembling Reed-Sternberg cells. The pattern of mesenteric node infiltration in the MTLs was also unusual in that preservation of the medullary sinuses was a common finding. A notable feature of the MTLs was the presence of a heavy infiltration of mature-looking plasma cells associated with a fairly severe villous atrophy in the lamina propria of the small bowel. In the WTLs the adjacent small bowel did not show this feature. In addition to the above cases three patients with a similar heavy plasma cell infiltrate and villous atrophy but without evidence of a lymphoma are described. These cases may represent examples of MTL in a pre-malignant phase. Also included in this study are three patients with alpha-chain disease (alpha-CD), all with a heavy plasma cell infiltration and villous atrophy of the lamina propria and a pleomorphic type lymphoma involving the mesenteric nodes in all, and the small bowel in two. The lymphomas in alpha-CD have been interpreted as immunoblastic sarcoma by Lukes and Collins. Both genetic and environmental factors may be operative in the MTLs including the cases of alpha-CD.
将17例“西方”型原发性腹部淋巴瘤(WTL)的临床和病理特征与14例“地中海”型(MTL)进行比较。MTL仅累及年轻成年混血儿和非洲患者,其主要临床特征为吸收不良和腹痛。WTL也主要影响混血儿患者,但有4例发生在白种人身上,就诊时的平均年龄晚了20年。梗阻性表现最为常见;该组中只有1例患者有吸收不良的证据。WTL主要位于远端小肠,几乎均为单形性淋巴细胞或组织细胞型。MTL主要位于十二指肠和空肠,为不寻常的多形性组织学类型。可见一系列细胞,从类似非典型淋巴细胞的细胞到大型组织细胞类型,后者一些类似里德 - 斯腾伯格细胞。MTL中肠系膜淋巴结浸润模式也不寻常,即髓窦保留是常见表现。MTL的一个显著特征是存在大量外观成熟的浆细胞浸润,同时小肠固有层有相当严重的绒毛萎缩。在WTL中,相邻小肠未表现出此特征。除上述病例外,还描述了3例有类似大量浆细胞浸润和绒毛萎缩但无淋巴瘤证据的患者。这些病例可能代表MTL的癌前阶段实例。本研究还包括3例α链病(α - CD)患者,均有大量浆细胞浸润和固有层绒毛萎缩,所有患者均有多形性淋巴瘤累及肠系膜淋巴结,2例累及小肠。Lukes和Collins将α - CD中的淋巴瘤解释为免疫母细胞肉瘤。遗传和环境因素可能在MTL包括α - CD病例中起作用。