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台湾地区含有里德-斯腾伯格样巨细胞的霍奇金病和非霍奇金淋巴瘤。50例临床病理分析

Hodgkin's disease and non-Hodgkin's lymphoma containing Reed-Sternberg-like giant cells in Taiwan. A clinicopathologic analysis of 50 cases.

作者信息

Hong R L, Su I J, Chen Y C, Hsieh H C, Wang C H, Liu C H, Shen M C

机构信息

Department of Internal Medicine, National Taiwan University, Taipei, Republic of China.

出版信息

Cancer. 1992 Mar 1;69(5):1254-8. doi: 10.1002/cncr.2820690530.

Abstract

Hodgkin's disease (HD) is uncommon in Taiwan. In reviewing the clinicopathologic features of 50 cases, the authors found that the diagnosis of HD was complicated with non-Hodgkin's lymphoma (NHL). Fourteen cases were reclassified as NHL containing Reed-Sternberg (RS) giant cells, mostly peripheral T-cell lymphoma (PTL), and 34 cases as classic HD, which included 8 cases of lymphocyte predominance, 10 of nodular sclerosis, 12 of mixed cellularity, and 4 of lymphocyte depletion. For cases of HD, there was a bimodal age-incidence distribution with peaks at the third and fifth decades; 61.8% manifested Stage B symptoms and 80.6% had Stage III/IV disease. The group of patients with NHL, compared with those with classic HD, was found to be older (mean age, 41.4 years versus 33.1 years; P less than 0.05), to have more extranodal disease (35.7% versus 8.8%, P less than 0.05), less complete remission rate (25% versus 67.9%, P less than 0.05), and shorter median survival (29 months versus 90 months). Most of the NHL patients originally were diagnosed as having atypical or unclassified HD. Thus, the authors conclude that the previous observation of a predominance of mixed cellularity HD in Asian regions may be attributable to the inclusion of PTL, which may mimic HD in histology. Because there is a marked difference in clinical behavior and prognosis, it is important to distinguish between HD and NHL containing RS giant cells in an area with a high incidence of PTL.

摘要

霍奇金淋巴瘤(HD)在台湾并不常见。通过回顾50例患者的临床病理特征,作者发现HD的诊断常与非霍奇金淋巴瘤(NHL)混淆。14例被重新分类为含有里德-斯腾伯格(RS)巨细胞的NHL,其中大多数为外周T细胞淋巴瘤(PTL),34例为经典型HD,包括8例淋巴细胞为主型、10例结节硬化型、12例混合细胞型和4例淋巴细胞消减型。HD患者的年龄发病率呈双峰分布,高峰出现在第三个和第五个十年;61.8%表现为B期症状,80.6%为III/IV期疾病。与经典型HD患者相比,NHL患者年龄更大(平均年龄41.4岁对33.1岁;P<0.05),结外病变更多(35.7%对8.8%,P<0.05),完全缓解率更低(25%对67.9%,P<0.05),中位生存期更短(29个月对90个月)。大多数NHL患者最初被诊断为非典型或未分类的HD。因此作者得出结论,之前观察到亚洲地区混合细胞型HD占优势可能归因于PTL的纳入,PTL在组织学上可能类似HD。由于临床行为和预后存在显著差异,在PTL高发地区区分HD和含有RS巨细胞的NHL很重要。

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