CNS erythroblastic sarcoma: a potential emerging pediatric tumor type characterized by NFIA::RUNX1T1/3 fusions.
Arnault Tauziède-EspariatLucille Lew-DerivrySamuel AbbouAlice MétaisGaëlle PierronStéphanie ReynaudJulien Masliah-PlanchonCassandra MarietLauren HastyVolodia Dangouloff-RosNathalie BoddaertMarie CsanyiAude Aline-FardinClaire LamaisonFabrice ChrétienKévin BeccariaStéphanie PugetPascale VarletPublished in: Acta neuropathologica communications (2024)
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.
Keyphrases
- acute myeloid leukemia
- bone marrow
- transcription factor
- blood brain barrier
- dna methylation
- induced apoptosis
- soft tissue
- allogeneic hematopoietic stem cell transplantation
- middle aged
- nk cells
- poor prognosis
- dendritic cells
- mesenchymal stem cells
- gene expression
- ms ms
- genome wide
- mass spectrometry
- cell cycle arrest
- small cell lung cancer
- endoplasmic reticulum stress
- climate change
- cell proliferation
- pi k akt
- immune response