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Classification of AIDS‐related lymphoma cases between 1987 and 2012 in Japan based on the WHO classification of lymphomas, fourth edition

机译:基于WHO淋巴瘤分类,日本于1987年至2012年间与AIDS相关的淋巴瘤病例分类

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AbstractThe introduction of combined antiretroviral therapy (ART) has reduced the mortality of patients with human immunodeficiency virus-1 infection worldwide. However, malignant lymphoma is a severe and frequent complication seen in patients with acquired immunodeficiency syndrome (AIDS). The diagnostic criteria for some categories of AIDS-related lymphoma were revised in the World Health Organization International Classification of Lymphoma, fourth edition. The purpose of this study was to assess the clinicopathological characteristics of Japanese patients with AIDS-related lymphoma according to the revised classification. In this retrospective study, 207 AIDS-related lymphoma cases diagnosed between 1987 and 2012 in Japan were subjected to histological subtyping and clinicopathological analyses. Diffuse large B-cell lymphoma (DLBCL) was the predominant histological subtype throughout the study period (n = 104, 50%). Among the DLBCL cases, 24% were of the germinal center (GC) type and 76% were of the non-GC type. Non-GC-type cases showed a significantly lower 1-year survival rate (43%) than the GC-type cases (82%). Cases of Burkitt lymphoma (n = 57, 28%), plasmablastic lymphoma (n = 16, 8%), primary effusion lymphoma (n = 9, 4%), Hodgkin lymphoma (n = 8, 4%), and large B-cell lymphoma arising in Kaposi sarcoma-associated herpesvirus-associated multicentric Castleman disease (n = 2, 1%) were also observed. Hodgkin lymphoma was more common in patients receiving ART (11.1%) than in ART-naïve patients (1.4%). Statistical analyses identified CD10 negativity, BCL-6 negativity, Epstein–Barr virus positivity, and Kaposi sarcoma-associated herpesvirus positivity as risk factors for poor prognosis. This information will help in the early diagnosis of lymphoma in patients with AIDS.
机译:摘要联合抗逆转录病毒疗法(ART)的引入降低了全世界人类免疫缺陷病毒1感染患者的死亡率。然而,恶性淋巴瘤是一种严重且常见的并发症,发生在获得性免疫缺陷综合症(AIDS)患者中。某些与艾滋病有关的淋巴瘤的诊断标准在世界卫生组织国际淋巴瘤分类第四版中进行了修订。这项研究的目的是根据修订后的分类评估日本艾滋病相关淋巴瘤患者的临床病理特征。在这项回顾性研究中,对1987年至2012年在日本诊断的207例与艾滋病相关的淋巴瘤病例进行了组织学分型和临床病理分析。在整个研究期间,弥漫性大B细胞淋巴瘤(DLBCL)是主要的组织学亚型(n = 104,50%)。在DLBCL病例中,生发中心(GC)型为24%,非GC型为76%。非GC型病例的1年生存率(43%)明显低于GC型病例(82%)。伯基特淋巴瘤(n = 57,28%),浆母细胞性淋巴瘤(n = 16,8%),原发性渗出性淋巴瘤(n = 9、4%),霍奇金淋巴瘤(n = 8、4%)和大B的病例还观察到在卡波西氏肉瘤相关的疱疹病毒相关的多中心卡斯尔曼病(n = 2,1%)中发生的细胞淋巴瘤。接受ART的患者中的霍奇金淋巴瘤(11.1%)比没有接受过ART的患者(1.4%)更为常见。统计分析确定CD10阴性,BCL-6阴性,爱泼斯坦-巴尔病毒阳性和卡波西肉瘤相关疱疹病毒阳性是不良预后的危险因素。这些信息将有助于艾滋病患者的淋巴瘤的早期诊断。

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