CNS erythroblastic sarcoma: a potential emerging pediatric tumor type characterized by NFIA::RUNX1T1/3 fusions.

CNS leukemia Central nervous system Myeloid sarcoma NFIA::RUNX1T1

Journal

Acta neuropathologica communications
ISSN: 2051-5960
Titre abrégé: Acta Neuropathol Commun
Pays: England
ID NLM: 101610673

Informations de publication

Date de publication:
19 Jan 2024
Historique:
received: 10 11 2023
accepted: 10 12 2023
medline: 20 1 2024
pubmed: 20 1 2024
entrez: 19 1 2024
Statut: epublish

Résumé

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.

Identifiants

pubmed: 38243303
doi: 10.1186/s40478-023-01708-5
pii: 10.1186/s40478-023-01708-5
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

12

Informations de copyright

© 2023. The Author(s).

Références

WHO Classification of Tumours Editorial Board (2022) Haematolymphoid Tumours. Lyon (France): International Agency for Research on Cancer. WHO classification of tumours series, 5th Edn. Vol. 11
Yang Y, Shu Y, Tang Y, Zhao S, Jia Y, Ji J et al (2023) RNA sequencing of myeloid sarcoma, shed light on myeloid sarcoma stratification. Cancer Med 12(8):9156–9166
doi: 10.1002/cam4.5654 pubmed: 36916780 pmcid: 10166975
Grier HE, Krailo MD, Tarbell NJ, Link MP, Fryer CJH, Pritchard DJ et al (2003) Addition of ifosfamide and etoposide to standard chemotherapy for Ewing’s sarcoma and primitive neuroectodermal tumor of bone. N Engl J Med 348(8):694–701
doi: 10.1056/NEJMoa020890 pubmed: 12594313
Chisholm KM, Heerema-McKenney AE, Choi JK, Smith J, Ries RE, Hirsch BA et al (2020) Acute erythroid leukemia is enriched in NUP98 fusions: a report from the children’s oncology group. Blood Adv 4(23):6000–6008
doi: 10.1182/bloodadvances.2020002712 pubmed: 33284945 pmcid: 7724911
Linnik Y, Pastakia D, Dryden I, Head DR, Mason EF (2020) Primary central nervous system erythroid sarcoma with NFIA-CBFA2T3 translocation: a rare but distinct clinicopathologic entity. Am J Hematol 95(11):E299-301
doi: 10.1002/ajh.25944 pubmed: 32697373
Liu H, Guinipero TL, Schieffer KM, Carter C, Colace S, Leonard JR et al (2020) De novo primary central nervous system pure erythroid leukemia/sarcoma with t(1;16)(p31;q24) NFIA/CBFA2T3 translocation. Haematologica Avr 105(4):e194–e197
doi: 10.3324/haematol.2019.231928
King RL, Siaghani PJ, Wong K, Edlefsen K, Shane L, Howard MT et al (2021) Novel t(1;8)(p31.3;q21.3) NFIA-RUNX1T1 translocation in an infant erythroblastic sarcoma. Am J Clin Pathol 156(1):129–138
doi: 10.1093/ajcp/aqaa216 pubmed: 33313700
Vodyanik MA, Thomson JA, Leukosialin Slukvin II. (2006) (CD43) defines hematopoietic progenitors in human embryonic stem cell differentiation cultures. Blood 108(6):2095–2105
doi: 10.1182/blood-2006-02-003327 pubmed: 16757688 pmcid: 1895535
Ohgami RS, Chisholm KM, Ma L, Arber DA (2014) E-cadherin is a specific marker for erythroid differentiation and has utility, in combination with CD117 and CD34, for enumerating myeloblasts in hematopoietic neoplasms. Am J Clin Pathol Mai 141(5):656–664
doi: 10.1309/AJCP8M4QQTAZPGRP

Auteurs

Arnault Tauziède-Espariat (A)

Department of Neuropathology, GHU Paris-Psychiatrie et Neurosciences, Sainte-Anne Hospital, 1, rue Cabanis, 75014, Paris, France. a.tauziede-espariat@ghu-paris.fr.
Inserm, UMR 1266, IMA-Brain, Institut de Psychiatrie et Neurosciences de Paris, Paris, France. a.tauziede-espariat@ghu-paris.fr.

Lucille Lew-Derivry (L)

Department of Hematology and Pediatric Oncology, Armand Trousseau Hospital, Paris, France.

Samuel Abbou (S)

Children and Adolescent Oncology Department, INSERM U1015, Paris-Saclay University, Villejuif, France.

Alice Métais (A)

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.

Gaëlle Pierron (G)

Paris-Sciences-Lettres, Curie Institute Research Center, INSERMU830, Paris, France.
Laboratory of Somatic Genetics, Curie Institute Hospital, Paris, France.

Stéphanie Reynaud (S)

Laboratory of Somatic Genetics, Curie Institute Hospital, Paris, France.

Julien Masliah-Planchon (J)

Laboratory of Somatic Genetics, Curie Institute Hospital, Paris, France.

Cassandra Mariet (C)

Department of Neuropathology, GHU Paris-Psychiatrie et Neurosciences, Sainte-Anne Hospital, 1, rue Cabanis, 75014, Paris, France.

Lauren Hasty (L)

Department of Neuropathology, GHU Paris-Psychiatrie et Neurosciences, Sainte-Anne Hospital, 1, rue Cabanis, 75014, Paris, France.

Volodia Dangouloff-Ros (V)

Pediatric Radiology Department, Hôpital Necker Enfants Malades, AP-HP, Paris, France.
UMR 1163, Institut Imagine and INSERM U1299, Université Paris Cité, Paris, France.

Nathalie Boddaert (N)

Pediatric Radiology Department, Hôpital Necker Enfants Malades, AP-HP, Paris, France.
UMR 1163, Institut Imagine and INSERM U1299, Université Paris Cité, Paris, France.

Marie Csanyi (M)

Institute of Pathology, Centre de Biologie Pathologie, Lille University Hospital, 59000, Lille, France.

Aude Aline-Fardin (A)

Department of Pathology, CHU de La Martinique, Fort-de-France, France.

Claire Lamaison (C)

Department of Pathology, Henri Mondor Hospital, APHP, Créteil, France.

Fabrice Chrétien (F)

Department of Neuropathology, GHU Paris-Psychiatrie et Neurosciences, Sainte-Anne Hospital, 1, rue Cabanis, 75014, Paris, France.

Kévin Beccaria (K)

Department of Pediatric Neurosurgery, Necker Hospital, APHP, Université Paris Descartes, Sorbonne Paris Cite, 75015, Paris, France.

Stéphanie Puget (S)

Department of Pediatric Neurosurgery, CHU de La Martinique, Fort-de-France, France.

Pascale Varlet (P)

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.

Classifications MeSH