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非霍奇金淋巴瘤组织学进展的尸检研究。来自美国国立癌症研究所的192例病例。

An autopsy study of histologic progression in non-Hodgkin's lymphomas. 192 cases from the National Cancer Institute.

作者信息

Garvin A J, Simon R M, Osborne C K, Merrill J, Young R C, Berard C W

出版信息

Cancer. 1983 Aug 1;52(3):393-8. doi: 10.1002/1097-0142(19830801)52:3<393::aid-cncr2820520302>3.0.co;2-m.

Abstract

Histologic slides were reviewed from 192 autopsies of patients with non-Hodgkin's lymphomas admitted to the National Cancer Institute (NCI) from 1953 to 1975. Each autopsy was classified according to the systems of Rappaport and Lukes-Collins. Comparisons with the initial diagnosis were made. The initial histologic diagnoses of the autopsied population were similar in distribution to other published series of non-Hodgkin's lymphomas. Of the 56 cases which initially demonstrated nodular patterns of growth, the following distribution was found at autopsy: 25%, no lymphoma; 6%, nodular lymphoma; 32%, diffuse histiocytic (large cell) lymphoma (DHL); 21%, diffuse undifferentiated (non-Burkitt's) lymphoma (DUL); and 16%, the remaining diffuse morphologies. Of the 136 patients with initial diagnosis of diffuse lymphoma, the following distributions were observed at autopsy: 20%, no lymphoma; 0%, nodular lymphoma; 31%, diffuse histiocytic (large cell) lymphoma; 12%, diffuse undifferentiated (non-Burkitt's) lymphoma; 9%, Burkitt's tumor; 14%, diffuse poorly differentiated lymphocytic lymphoma; and 14%, the remaining diffuse morphologic types. One hundred and thirty-four cases which were initially diagnosed as follicular center cell type within the Lukes-Collins classification gave the following distribution at autopsy: 21%, no lymphoma; 25%, small noncleaved type; 17%, large noncleaved type; 23%, non-follicular center cell lymphomas (17% immunoblastic B); and the remaining 13% were distributed among the other follicular center cell types. This autopsy review demonstrates the rarity of nodular (follicular) lymphomas at autopsy, and the predominance of the diffuse histiocytic or "transformed" type. This study provides a comparison of the rate of histologic progression of lymphomas in the same patient population at autopsy with a previously published study of progression during life.

摘要

对1953年至1975年期间入住美国国立癌症研究所(NCI)的192例非霍奇金淋巴瘤患者的尸检组织切片进行了回顾。每次尸检均根据拉帕波特(Rappaport)和卢克斯-柯林斯(Lukes-Collins)系统进行分类。并与初始诊断进行了比较。尸检人群的初始组织学诊断在分布上与其他已发表的非霍奇金淋巴瘤系列相似。在最初表现为结节状生长模式的56例病例中,尸检时发现以下分布情况:25%为无淋巴瘤;6%为结节性淋巴瘤;32%为弥漫性组织细胞(大细胞)淋巴瘤(DHL);21%为弥漫性未分化(非伯基特氏)淋巴瘤(DUL);16%为其余弥漫性形态。在最初诊断为弥漫性淋巴瘤的136例患者中,尸检时观察到以下分布情况:20%为无淋巴瘤;0%为结节性淋巴瘤;31%为弥漫性组织细胞(大细胞)淋巴瘤;12%为弥漫性未分化(非伯基特氏)淋巴瘤;9%为伯基特氏肿瘤;14%为弥漫性低分化淋巴细胞淋巴瘤;14%为其余弥漫性形态类型。在卢克斯-柯林斯分类中最初诊断为滤泡中心细胞型的134例病例,尸检时分布如下:21%为无淋巴瘤;25%为小无裂细胞型;17%为大无裂细胞型;23%为非滤泡中心细胞淋巴瘤(17%为免疫母细胞性B);其余13%分布于其他滤泡中心细胞类型。本次尸检回顾显示,尸检时结节性(滤泡性)淋巴瘤罕见,弥漫性组织细胞型或“转化”型占主导。本研究将同一患者群体尸检时淋巴瘤的组织学进展率与先前发表的关于生前进展情况的研究进行了比较。

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