Myelodysplastic neoplasms evolving from inherited bone marrow failure syndromes / germline predisposition syndromes: Back under the microscope

Leuk Res. 2024 Feb:137:107441. doi: 10.1016/j.leukres.2024.107441. Epub 2024 Jan 23.

Abstract

Inherited bone marrow failure syndromes and germline predisposition syndromes (IBMFS/GPS) are associated with increased risk for hematologic malignancies, particularly myeloid neoplasms, such as myelodysplastic neoplasms (MDS) and acute myeloid leukemia (AML). The diagnosis of MDS in these syndromes poses difficulty due to frequent bone marrow hypocellularity and the presence of some degree of dysplastic features related to the underlying germline defect causing abnormal maturation of one or more cell lines. Yet, the diagnosis of MDS is usually associated with a worse outcome in several IBMFS/GPS. Criteria for the diagnosis of MDS in IBMFS/GPS have not been standardized with some authors suggesting a mixture of morphologic, cytogenetic, and genetic criteria. This review highlights these challenges and suggests a more standardized approach to nomenclature and diagnostic criteria.

Keywords: Bone marrow; Cytogenetics; Germline predisposition; Inherited bone marrow failure; Myelodysplastic syndrome clonal evolution.

Publication types

  • Review

MeSH terms

  • Bone Marrow Diseases* / complications
  • Bone Marrow Diseases* / genetics
  • Bone Marrow Diseases* / pathology
  • Congenital Bone Marrow Failure Syndromes / complications
  • Genetic Predisposition to Disease
  • Germ Cells / pathology
  • Humans
  • Leukemia, Myeloid, Acute* / genetics
  • Myelodysplastic Syndromes* / diagnosis
  • Myelodysplastic Syndromes* / genetics
  • Myelodysplastic Syndromes* / pathology