Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Mod Pathol. 2011 Mar;24(3):355-66. doi: 10.1038/modpathol.2010.206. Epub 2010 Nov 19.
Dura-based marginal zone lymphomas represent an uncommon group of low-grade B-cell neoplasms, and literature regarding the clinical, histological and genetic profile of these tumors in the context of the newly described IgG4-related entities is lacking. We analyzed 32 dura-based marginal zone lymphomas identified in 27 females and 5 males ranging in age from 33-82 years (median 50). Morphologic examination, immunohistochemical studies and PCR for B-cell clonality were carried out in all cases. In addition, IgG4 immunohistochemistry and cytogenetic studies (either by FISH or RT-PCR) were carried out in 20 (18 primary dural; 2 with associated extradural disease) and 9 cases, respectively. Clinically, most cases presented radiologically as dura-based masses, mimicking meningioma. Histologically, the majority exhibited plasmacytoid differentiation, and were clonal either by PCR or immunohistochemical light chain analysis (28 out of 32). In the subset tested for IgG4, 6 of 18 primary dural marginal zone lymphoma (including one epidural tumor) showed numerous IgG4-positive plasma cells; all 6 were light chain restricted and clonal by PCR in 5 of 6 tested cases. Three IgG4-positive marginal zone lymphomas tested for cytogenetics did not show any cytogenetic aberrations. Across all cases, FISH and RT-PCR identified abnormalities in three out of nine cases (trisomies 3 and 18; trisomies 3 and 1; trisomy 18) without any extranodal marginal zone lymphoma specific translocations. Regardless of the treatment modality, 16 of 17 patients with follow-up are alive without evidence of disease over a period of 4-124 months (median 19.5). The expression of IgG4 in light-chain-restricted clonal plasma cells of a significant subset of dural marginal zone lymphomas, including one in an epidural location, is a novel finding and points to distinctive biology. Cytogenetic aberrations are present only in a minority of dural marginal zone lymphomas.
硬脑膜边缘区淋巴瘤是一组罕见的低级 B 细胞肿瘤,关于这些肿瘤在新描述的 IgG4 相关实体中的临床、组织学和遗传学特征的文献尚缺乏。我们分析了 32 例硬脑膜边缘区淋巴瘤,这些病例来自 27 名女性和 5 名男性,年龄 33-82 岁(中位数为 50 岁)。所有病例均进行了形态学检查、免疫组织化学研究和 B 细胞克隆性 PCR。此外,在 20 例(18 例原发性硬脑膜;2 例伴硬膜外疾病)和 9 例病例中分别进行了 IgG4 免疫组化和细胞遗传学研究(分别通过 FISH 或 RT-PCR)。临床上,大多数病例在影像学上表现为硬脑膜为基础的肿块,类似于脑膜瘤。组织学上,大多数病例表现为浆细胞样分化,通过 PCR 或免疫组织化学轻链分析呈克隆性(32 例中有 28 例)。在 IgG4 检测的亚组中,18 例原发性硬脑膜边缘区淋巴瘤中有 6 例(包括 1 例硬膜外肿瘤)显示大量 IgG4 阳性浆细胞;所有 6 例均为轻链限制性,且在 6 例检测病例中有 5 例为 PCR 克隆性。在 3 例进行细胞遗传学检测的 IgG4 阳性边缘区淋巴瘤中,均未发现任何细胞遗传学异常。在所有病例中,FISH 和 RT-PCR 在 9 例中的 3 例中发现了异常(三体 3 和 18;三体 3 和 1;三体 18),但没有任何结外边缘区淋巴瘤特异性易位。无论治疗方式如何,17 例有随访记录的患者中有 16 例在 4-124 个月(中位数为 19.5 个月)的时间内无疾病证据而存活。在显著数量的硬脑膜边缘区淋巴瘤中,包括一个硬膜外位置的肿瘤,轻链限制性克隆性浆细胞表达 IgG4 是一个新发现,提示其具有独特的生物学特性。细胞遗传学异常仅存在于少数硬脑膜边缘区淋巴瘤中。