Department of Pathology, Centre of Oncology, Maria Skłodowska-Curie Memorial Institute, Warsaw, Poland.
Med Oncol. 2006;23(3):423-8. doi: 10.1385/MO:23:3:423.
We report a case of 43-yr-old Caucasian female with an unusual, cyclin D1 positive marginal zone lymphoma (MZL) of mucosa-associated lymphoid tissue (MALT) type of the mediastinum. To date, only about 30 cases of this entity have been published. They occur mainly in Asian females with a history of coexisting autoimmune disease. To our knowledge, this is the first case of mediastinal MZL with cyclin D1 expression. In the span of 6 yr this patient's tumor recurred three times, was surgically treated, and initially diagnosed as paraganglioma. The diagnosis was based on histopathological examination only. Our final diagnosis of MZL was made by combined evaluation of histopathology (HP), immunohistochemistry (IH), flow cytometry (FCM), fluorescence in situ hybridization (FISH), and molecular biology studies. We found a positive cyclin D1 reaction by IH and cyclin D1 mRNA (CCND1) overexpression by reverse transcription polymerase chain reaction (RT-PCR). Very high cyclin D1 to beta-actin mRNA ratio in this case was comparable with the ratio, characteristic for mantle cell lymphoma (MCL). However, there was no translocation t(11;14) found by FISH and an immunophenotype by IH and FCM was consistent with MZL ruling out MCL diagnosis. In addition, our case differs from other, previously reported thymic MZL lymphoma cases by no autoimmune disease association, Caucasian origin, and the absence of the plasmacytic differentiation on both HP/IH.
我们报告了一例 43 岁的高加索女性,患有罕见的、cyclin D1 阳性的结外边缘区淋巴瘤(MALT 型)纵隔型。迄今为止,仅有约 30 例此类病例被报道。它们主要发生在伴有自身免疫性疾病的亚洲女性中。据我们所知,这是首例纵隔 MALT 伴 cyclin D1 表达的病例。在 6 年的时间里,该患者的肿瘤复发了 3 次,接受了手术治疗,最初被诊断为副神经节瘤。该诊断仅基于组织病理学检查。我们对 MZL 的最终诊断是通过组织病理学(HP)、免疫组织化学(IH)、流式细胞术(FCM)、荧光原位杂交(FISH)和分子生物学研究的综合评估得出的。我们发现 IH 中 cyclin D1 反应阳性,逆转录聚合酶链反应(RT-PCR)中 cyclin D1 mRNA(CCND1)过表达。在这种情况下,cyclin D1 与β-肌动蛋白 mRNA 的比值非常高,与套细胞淋巴瘤(MCL)的比值相似。然而,通过 FISH 未发现易位 t(11;14),IH 和 FCM 的免疫表型与 MZL 一致,排除了 MCL 的诊断。此外,我们的病例与其他先前报道的胸内 MZL 淋巴瘤病例不同,无自身免疫性疾病相关,为白种人起源,且在 HP/IH 上均无浆细胞分化。