Suppr超能文献

儿童睾丸髓肉瘤:伴有 KMT2A(MLL)基因重排相关性的临床病理和免疫组织化学特征。

Myeloid Sarcoma of the Testis in Children: Clinicopathologic and Immunohistochemical Characteristics With KMT2A (MLL) Gene Rearrangement Correlation.

机构信息

Department of Pathology, Molecular and Cell-Based Medicine, Icahn School of Medicine at Mount Sinai.

Division of Hematology/Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York.

出版信息

Appl Immunohistochem Mol Morphol. 2020 Aug;28(7):501-507. doi: 10.1097/PAI.0000000000000783.

Abstract

Myeloid sarcoma (MS) is defined as an extramedullary mass-forming lesion composed of immature myeloid cells. It is a rare but well-known manifestation of acute myeloid leukemia. Pediatrics testicular MS may pose a possible diagnostic challenge, an issue that is underscored in the few testicular pediatric MS cases reported in the literature. Herein, we report a series of 5 cases of pediatric testicular MS that are evaluated at the morphologic and immunohistochemical levels with correlation with the KMT2A (MLL) rearrangement status. Three patients presented with no prior history of acute myeloid leukemia. All 5 cases showed monoblastic morphology; positive for CD33, CD43, CD68, CD163, CD4 (dim), and lysozyme; and negative for CD10, CD34, CD117, and myeloperoxidase. KMT2A (MLL) rearrangement was detected in 4 of the 5 cases. In the literature, 8 more cases of pediatric testicular lymphoma were reported. Most of them showed monocytic differentiation and KMT2A (MLL) rearrangement was reported in 3 of the cases. In conclusions, testicular MS in pediatric patients shows monoblastic differentiation which may be attributed to the KMT2A (MLL) rearrangement. We also highlight the importance of using an extended immunohistochemistry panel in the diagnosis of MS.

摘要

骨髓肉瘤 (MS) 定义为由未成熟髓细胞组成的骨髓外肿块形成病变。它是急性髓细胞白血病的一种罕见但众所周知的表现。儿科睾丸 MS 可能构成可能的诊断挑战,这在文献中报道的少数儿科睾丸 MS 病例中得到强调。在此,我们报告了一系列 5 例儿科睾丸 MS 的病例,这些病例在形态学和免疫组织化学水平上进行了评估,并与 KMT2A (MLL) 重排状态相关。有 3 名患者没有急性髓细胞白血病的既往病史。所有 5 例均显示单核母细胞形态;CD33、CD43、CD68、CD163、CD4(弱表达)和溶菌酶阳性;CD10、CD34、CD117 和髓过氧化物酶阴性。在 5 例中的 4 例中检测到 KMT2A (MLL) 重排。在文献中,还报道了 8 例儿科睾丸淋巴瘤病例。它们大多数表现为单核细胞分化,其中 3 例报告了 KMT2A (MLL) 重排。总之,儿科患者的睾丸 MS 显示单核母细胞分化,这可能归因于 KMT2A (MLL) 重排。我们还强调了在 MS 诊断中使用扩展免疫组织化学面板的重要性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验