Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Mod Pathol. 2011 Dec;24(12):1586-97. doi: 10.1038/modpathol.2011.116. Epub 2011 Aug 5.
The term gray zone lymphoma has been applied to tumors that demonstrate transitional morphologic and immunophenotypic features between classical Hodgkin's lymphoma and diffuse large B-cell lymphoma, especially primary mediastinal large B-cell lymphoma. Histopathological and genetic data are limited for these unusual cases. We analyzed cases of gray zone lymphoma (n=27), mediastinal composite lymphoma (n=3) and mediastinal synchronous/metachronous lymphoma (n=3) by morphology, immunophenotyping and fluorescence in situ hybridization. Mediastinal involvement was assured in 24/33 patients (73%). The patient cohort showed a male predominance (M:F ratio; 20:13) and a median age of 32 years (range, 16-91 years). Patients with mediastinal disease were significantly younger (median age: 29.5 years) than patients presenting without evident mediastinal disease (median age: 55 years). Gains including amplifications in 2p16.1 (REL/BCL11A locus) were observed in 33% of all patients, whereas alterations affecting the JAK2/PDL2 locus in 9p24.1 were present in 55%. Further studies revealed rearrangement of the CIITA locus at 16p13.13 in 8/30 cases (27%) and 7/26 cases (27%) demonstrated gains of 8q24 (MYC). Genetic aberrations involving 2p16.1, 9p24.1 and 8q24 showed a higher incidence in cases with evident mediastinal involvement. However, this was not statistically significant when compared with cases without known mediastinal involvement. Twelve of the 27 cases of gray zone lymphoma were morphologically more reminiscent of classical Hodgkin's lymphoma, whereas the other gray zone lymphomas presented with morphological features more closely resembling large B-cell lymphoma. Both morphological groups of gray zone lymphoma were similarly positive for Cyclin E (75 and 93%) and p63 (50 and 53%, respectively) expression. These findings further support a close relationship between gray zone lymphoma, classical Hodgkin's lymphoma and primary mediastinal large B-cell lymphoma, and suggest that some cases of gray zone lymphoma without mediastinal disease may share similar genetic alterations.
灰色区域淋巴瘤这一术语已被应用于那些形态学和免疫表型特征在经典霍奇金淋巴瘤和弥漫性大 B 细胞淋巴瘤之间具有过渡性的肿瘤,尤其是原发性纵隔大 B 细胞淋巴瘤。这些不常见病例的组织病理学和遗传学数据有限。我们通过形态学、免疫表型和荧光原位杂交分析了 27 例灰色区域淋巴瘤、3 例纵隔复合淋巴瘤和 3 例纵隔同步/异时性淋巴瘤。24/33 例患者(73%)有纵隔受累。该患者队列表现出男性为主(男:女比例为 20:13),中位年龄为 32 岁(范围,16-91 岁)。有纵隔疾病的患者明显比没有明显纵隔疾病的患者年轻(中位年龄:29.5 岁)(中位年龄:55 岁)。所有患者中,33%观察到包括 2p16.1(REL/BCL11A 基因座)在内的增益,而 55%存在影响 9p24.1 中的 JAK2/PDL2 基因座的改变。进一步的研究显示,在 30 例中的 8 例(27%)和 26 例中的 7 例(27%)中,CIITA 基因座在 16p13.13 处发生重排,在 7/26 例(27%)中发现 8q24(MYC)的增益。在有明显纵隔受累的病例中,涉及 2p16.1、9p24.1 和 8q24 的遗传异常发生率更高。然而,与无已知纵隔受累的病例相比,这并没有统计学意义。27 例灰色区域淋巴瘤中有 12 例在形态学上更类似于经典霍奇金淋巴瘤,而其他灰色区域淋巴瘤的形态学特征更类似于大 B 细胞淋巴瘤。两个形态学组的灰色区域淋巴瘤 Cyclin E(75%和 93%)和 p63(50%和 53%)的表达均为阳性。这些发现进一步支持灰色区域淋巴瘤、经典霍奇金淋巴瘤和原发性纵隔大 B 细胞淋巴瘤之间的密切关系,并表明一些无纵隔疾病的灰色区域淋巴瘤可能具有相似的遗传改变。