Jaffe E S, Strauchen J A, Berard C W
Am J Clin Pathol. 1982 Jan;77(1):46-9. doi: 10.1093/ajcp/77.1.46.
Diffuse aggressive non-Hodgkin's lymphomas are immunologically and morphologically heterogeneous. Morphologic subclassifications have been proposed with a presumptive relationship to immunologic phenotype. Six histologic types were studied, four of presumed follicular origin (large cleaved, large non-cleaved, mixed follicular center cell, and blastic) and two of presumed nonfollicular origin (pleomorphic pyroninophilic and pleomorphic convoluted). Two of these follicular subtypes were found to be associated with the frequent presence of B-cell markers; large non-cleaved, six of seven; and blastic, four of six. However, four of nine T-cell lymphomas were misclassified as lesions of follicular center cell type, indicating the difficulty of distinguishing some convoluted cells of T-cell lymphoma from irregularly cleaved cells of follicular lymphoma. Pleomorphic pyroninophilic or B-immunoblastic morphology was associated with B-cell markers in only two of six cases; two additional cases had T-cell markers, one had histiocytic markers and in one case, no markers were demonstrable. Thus, this morphology may reflect a common pathway of transformed lymphoid cells. Some cases of T-cell origin could be recognized by the striking pleomorphic convoluted histology (three of five cases) but morphologic overlap with pleomorphic B-cell tumors, particularly transformed nodular lymphomas, posed a problem. This histopathologic subclassification correctly predicted immunologic phenotype in only 61% of cases, suggesting that in diffuse non-Hodgkin's lymphomas, histologic appearance alone may not be a reliable indicator of immunologic surface markers.
弥漫性侵袭性非霍奇金淋巴瘤在免疫和形态学上具有异质性。已提出形态学亚分类,并假定其与免疫表型有关。研究了六种组织学类型,其中四种假定起源于滤泡(大裂细胞型、大无裂细胞型、混合滤泡中心细胞型和母细胞型),两种假定起源于非滤泡(多形性嗜派洛宁细胞型和多形性卷曲细胞型)。发现其中两种滤泡亚型经常出现B细胞标志物;大无裂细胞型,7例中有6例;母细胞型,6例中有4例。然而,9例T细胞淋巴瘤中有4例被错误分类为滤泡中心细胞型病变,这表明区分T细胞淋巴瘤的一些卷曲细胞与滤泡淋巴瘤的不规则裂细胞存在困难。多形性嗜派洛宁细胞型或B免疫母细胞形态仅在6例中的2例中与B细胞标志物相关;另外2例有T细胞标志物,1例有组织细胞标志物,1例未显示标志物。因此,这种形态可能反映了转化淋巴细胞的共同途径。一些T细胞起源的病例可通过显著的多形性卷曲组织学特征识别(5例中有3例),但与多形性B细胞肿瘤,特别是转化的结节性淋巴瘤的形态学重叠构成了一个问题。这种组织病理学亚分类仅在61%的病例中正确预测了免疫表型,这表明在弥漫性非霍奇金淋巴瘤中,仅组织学表现可能不是免疫表面标志物的可靠指标。