Pan Shien-Tung, Ko Young-Hyeh, Tan Soo-Yong, Chuang Shih-Sung
Department of Pathology, Tungs' Taichung MetroHarbor Hospital, Taichung, Taiwan.
Department of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Pathol Res Pract. 2018 Dec;214(12):2106-2109. doi: 10.1016/j.prp.2018.10.002. Epub 2018 Oct 21.
Primary cutaneous peripheral T-cell lymphomas (PC-PTCLs) are classified into mycosis fungoides (MF) and other rare specific types; and those do not fit into any specific entities are designated as PTCL, not otherwise specified (NOS), an aggressive neoplasm. Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL) is an aggressive primary intestinal T-cell lymphoma with enteropathy in the non-neoplastic mucosa. We report a rare case of PC-PTCL-NOS with a late relapse solely in the ileum after complete remission. We discuss the importance of evaluating enteropathy, megakaryocyte-associated tyrosine kinase (MATK) immunostaining, and the implication of clonal relationship of metachronous lymphomas.
We reviewed the histopathology and immunohistochemistry of the skin tumor from a 68-year-old female and the relapsed intestinal T-cell lymphoma. The tumor cells "trans-regressed" from large and pleomorphic in the skin to small/medium-sized cells with clear cytoplasm in the ileum; and furthermore, there was immunophenotypic alteration. However, there was no enteropathy in the non-tumoral ileal mucosa adjacent to the tumor proper and both the cutaneous and ileal tumors were negative for MATK. Clonality study showed clonal TRG and TRB rearrangement with identical band sizes of the amplicons, confirming primary cutaneous tumor with a late relapse in the ileum.
Although PC-PTCL-NOS is an aggressive neoplasm, rare cases such as this might have a long-term survival. Furthermore, the late relapse mimicking MEITL is intriguing and exceptional, in spite the fact that MEITL is a primary intestinal T-cell lymphoma with a typical histopathology and immunophenotype. Detailed clinicopathological and molecular studies are mandatory to elucidate the clonal relationship of metachronous lymphomas, as this has important clinical implication for treatment. Evaluation of the non-tumoral intestinal mucosa for enteropathy and immunostaining for MATK might help to differentiate a mimicker from a true MEITL.
原发性皮肤外周T细胞淋巴瘤(PC-PTCLs)分为蕈样肉芽肿(MF)和其他罕见的特定类型;那些不符合任何特定实体的则被指定为外周T细胞淋巴瘤,未另行指定(NOS),这是一种侵袭性肿瘤。单形性亲上皮性肠道T细胞淋巴瘤(MEITL)是一种侵袭性原发性肠道T细胞淋巴瘤,在非肿瘤性黏膜中伴有肠病。我们报告了一例罕见的PC-PTCL-NOS病例,在完全缓解后仅在回肠出现晚期复发。我们讨论了评估肠病、巨核细胞相关酪氨酸激酶(MATK)免疫染色的重要性,以及异时性淋巴瘤克隆关系的意义。
我们回顾了一名68岁女性皮肤肿瘤以及复发性肠道T细胞淋巴瘤的组织病理学和免疫组化结果。肿瘤细胞从皮肤中的大细胞和多形性细胞“逆分化”为回肠中具有清晰细胞质的小/中细胞;此外,存在免疫表型改变。然而,在与肿瘤相邻的非肿瘤性回肠黏膜中没有肠病,皮肤和回肠肿瘤的MATK均为阴性。克隆性研究显示TRG和TRB重排呈克隆性,扩增子的条带大小相同,证实原发性皮肤肿瘤在回肠出现晚期复发。
尽管PC-PTCL-NOS是一种侵袭性肿瘤,但这样的罕见病例可能有长期生存。此外,尽管MEITL是一种具有典型组织病理学和免疫表型的原发性肠道T细胞淋巴瘤,但这种类似MEITL的晚期复发很有趣且罕见。必须进行详细的临床病理和分子研究以阐明异时性淋巴瘤之间的克隆关系,因为这对治疗具有重要的临床意义。评估非肿瘤性肠道黏膜的肠病情况以及MATK免疫染色可能有助于区分模仿者与真正的MEITL。