Department of Neuropathology, GHU Paris-Psychiatrie et Neurosciences, Sainte-Anne Hospital, 1, rue Cabanis, 75014, Paris, France.
Inserm, UMR 1266, IMA-Brain, Institut de Psychiatrie et Neurosciences de Paris, Paris, France.
Acta Neuropathol Commun. 2024 Jan 19;12(1):12. doi: 10.1186/s40478-023-01708-5.
Erythroblastic sarcoma (ES) (previously called chloroma or granulocytic sarcoma) are rare hematological neoplams characterized by the proliferation of myeloid blasts at extramedullary sites, and primarily involve the skin and soft tissue of middle-aged adults. ES may be concomitant with or secondary to myeloid neoplasms (mostly acute myeloid leukemia (AML)) or in isolated cases (de novo) without infiltration of the bone marrow by blasts. ES share cytogenetic and molecular abnormalities with AML, including RUNX1T1 fusions. Some of these alterations seem to be correlated with particular sites of involvement. Herein, we report an isolated erythroblastic sarcoma with NFIA::RUNX1T1 located in the central nervous system (CNS) of a 3-year-old boy. Recently, two pediatric cases of CNS MS with complete molecular characterization have been documented. Like the current case, they concerned infants (2 and 3 years-old) presenting a brain tumor (pineal involvement) with leptomeningeal dissemination. Both cases also harbored a NFIA::RUNX1T3 fusion. ES constitutes a diagnostic challenge for neuropathologists because it does not express differentiation markers such as CD45, and may express CD99 which could be confused with CNS Ewing sarcoma. CD43 is the earliest pan-hematopoietic marker and CD45 is not expressed by erythroid lineage cells. E-cadherin (also a marker of erythroid precursors) and CD117 (expressed on the surface of erythroid lineage cells) constitute other immunhistochemical hallmarks of ES. The prognosis of patients with ES is similar to that of other patients with AML but de novo forms seem to have a poorer prognosis, like the current case. To conclude, pediatric ES with NFIA::RUNX1T1/3 fusions seem to have a tropism for the CNS and thus constitute a potential pitfall for neuropathologists. Due to the absence of circulating blasts and a DNA-methylation signature, the diagnosis must currently be made by highlighting the translocation and expression of erythroid markers.
红细胞肉瘤(ES)(以前称为粒细胞肉瘤或绿色瘤)是一种罕见的血液系统肿瘤,其特征是骨髓原始细胞在骨髓外部位增殖,主要累及中年成人的皮肤和软组织。ES 可能与髓系肿瘤(主要是急性髓系白血病(AML))同时发生或继发于髓系肿瘤,或在无原始细胞浸润骨髓的孤立病例(原发性)中发生。ES 与 AML 具有细胞遗传学和分子异常,包括 RUNX1T1 融合。这些改变中的一些似乎与特定的受累部位有关。本文报道了一例孤立性红细胞肉瘤,其 NFIA::RUNX1T1 位于 3 岁男孩的中枢神经系统(CNS)中。最近,有 2 例儿童 CNS MS 病例的分子特征已被记录。与当前病例一样,它们涉及 2 岁和 3 岁的婴儿,表现为脑肿瘤(松果体受累)伴软脑膜播散。这两个病例都存在 NFIA::RUNX1T3 融合。ES 对神经病理学家构成诊断挑战,因为它不表达分化标志物,如 CD45,并且可能表达 CD99,这可能与 CNS 尤文肉瘤混淆。CD43 是最早的全血细胞标志物,CD45 不表达于红细胞系细胞。E-钙粘蛋白(也是红细胞前体细胞的标志物)和 CD117(表达于红细胞系细胞表面)是 ES 的其他免疫组织化学特征。ES 患者的预后与其他 AML 患者相似,但原发性形式似乎预后较差,与当前病例一样。总之,具有 NFIA::RUNX1T1/3 融合的儿科 ES 似乎对 CNS 具有趋化性,因此对神经病理学家构成潜在陷阱。由于没有循环原始细胞和 DNA 甲基化特征,目前必须通过突出显示易位和红细胞标志物的表达来诊断。