Bateman A C, Wright D H
Department of Histopathology, Southampton General Hospital, UK.
Histopathology. 1993 Nov;23(5):409-15. doi: 10.1111/j.1365-2559.1993.tb00488.x.
Low-grade lymphomas of mucosa-associated lymphoid tissue (MALT) characteristically show centrocyte-like cells, plasmacytic differentiation, follicular colonization and lymphoepithelial lesions (epitheliotropism). High-grade lymphomas of MALT are thought to lack these features and can only be identified as MALT lymphomas with confidence if they are admixed with residual low-grade tumours. We studied 23 cases of MALT lymphoma of the thyroid. Six were predominantly low-grade, 12 were predominantly high-grade, and five contained both low- and high-grade areas. All cases were stained for cytokeratin, epithelial membrane antigen and laminin using an immunoperoxidase technique. The low-grade lymphomas all contained lymphoepithelial lesions, generally in the form of clusters of intra-acinar centrocyte-like cells. Eleven of the 12 high-grade MALT lymphomas of the thyroid also showed lymphoepithelial lesions. These appeared in three forms: follicles or clusters of epithelial cells infiltrated by groups of centrocyte-like cells, intra-acinar clusters of blast cells, or irregular invasion of islands of epithelial cells by blast cells. The first pattern presumably represented residual low-grade tumour over-run by high-grade lymphoma. The second two patterns indicated that the factors that result in epitheliotropism in low-grade MALT lymphomas are also present in high-grade tumours. Following this study we identified epitheliotropism in single examples of high-grade MALT lymphomas of the bronchus and small intestine. Previous failure to recognize epitheliotropism in high-grade MALT lymphomas of the gastrointestinal tract may be due to loss of the affected epithelium. The localization and relatively good prognosis of high-grade MALT lymphomas may be related to retention of MALT characteristics including epitheliotropism.
黏膜相关淋巴组织(MALT)低度淋巴瘤的特征是出现中心细胞样细胞、浆细胞分化、滤泡定植和淋巴上皮病变(亲上皮性)。MALT高度淋巴瘤被认为缺乏这些特征,只有当它们与残留的低度肿瘤混合时才能被明确诊断为MALT淋巴瘤。我们研究了23例甲状腺MALT淋巴瘤。6例主要为低度,12例主要为高度,5例同时含有低度和高度区域。所有病例均采用免疫过氧化物酶技术进行细胞角蛋白、上皮膜抗原和层粘连蛋白染色。低度淋巴瘤均有淋巴上皮病变,通常表现为腺泡内中心细胞样细胞簇。12例甲状腺高度MALT淋巴瘤中有11例也显示出淋巴上皮病变。这些病变有三种形式:被中心细胞样细胞群浸润的滤泡或上皮细胞簇、母细胞的腺泡内簇,或母细胞对上皮细胞岛的不规则浸润。第一种模式可能代表被高度淋巴瘤侵犯的残留低度肿瘤。后两种模式表明导致低度MALT淋巴瘤亲上皮性的因素在高度肿瘤中也存在。在这项研究之后,我们在支气管和小肠的高度MALT淋巴瘤的单个病例中发现了亲上皮性。之前未能在胃肠道高度MALT淋巴瘤中识别亲上皮性可能是由于受累上皮的丢失。高度MALT淋巴瘤的定位和相对较好的预后可能与包括亲上皮性在内的MALT特征的保留有关。