A five-case series demonstrates that morphological assessment extending beyond isolated cytologic features to include spatial distribution of cells, functional behavior, and bone marrow microenvironmental context remains central to the accurate diagnosis of aggressive malignancies.
Key Findings
Results
Bone marrow infiltration by dedifferentiated melanoma can mimic a hematologic neoplasm, with melanin-laden macrophages providing a critical diagnostic clue.
The case involved dedifferentiated melanoma infiltrating the bone marrow in a pattern resembling a hematologic neoplasm.
Melanin-laden macrophages were identified as a decisive morphological finding.
The case illustrates the importance of recognizing functional cellular features such as hemophagocytosis and pigment-laden cells in the bone marrow microenvironment.
Morphological clues in this case were described as 'subtle and often overlooked.'
Results
Carcinocythemia revealing metastatic melanoma was identified with neoplastic cells confined to smear edges.
Neoplastic cells were spatially restricted to the edges of the blood smear, representing an atypical localization pattern.
This case of carcinocythemia — circulating tumor cells in peripheral blood — was the presenting manifestation of metastatic melanoma.
The finding underscores that atypical spatial localization of tumor cells can provide decisive diagnostic information.
This case demonstrates that morphological examination must include assessment of cell distribution across the entire smear preparation.
Results
Anaplastic IgA multiple myeloma presented with striking cytological atypia in the bone marrow.
The myeloma was characterized as anaplastic with IgA isotype.
The case featured 'striking cytological atypia' as the predominant morphological finding.
This case is included as an example of a diagnostically challenging setting where morphological assessment is essential.
The case is presented within the context of requiring complementary immunophenotypic and molecular techniques alongside morphology.
Results
Acute monoblastic leukemia presented with a rapidly fatal clinical course.
The case was classified as acute monoblastic leukemia.
The disease course was described as 'rapidly fatal.'
This case is included as an example of an aggressive malignancy where morphological diagnosis is critical.
The case illustrates the role of morphological assessment in identifying aggressive malignancies requiring urgent clinical action.
Results
Myelodysplastic syndrome with SF3B1 mutation was characterized by prominent erythroblastic islands and subtle dysplasia.
The case carried an SF3B1 mutation, a recognized molecular marker in myelodysplastic syndrome.
Morphological features included 'prominent erythroblastic islands' and 'subtle dysplasia.'
The case highlights bone marrow microenvironmental context — specifically the organization of erythroblastic islands — as a diagnostically relevant morphological feature.
Subtle dysplasia in this case exemplifies findings that may be missed without a structured, contextual morphological approach.
Discussion
Atypical spatial localization of tumor cells, functional features such as hemophagocytosis, and microenvironmental alterations were identified as decisive diagnostic morphological parameters across the case series.
The paper argues that morphological assessment should extend beyond 'isolated cytologic features' to include 'spatial distribution of cells, functional behavior, and bone marrow microenvironmental context.'
Hemophagocytosis is cited as a specific functional feature with diagnostic relevance.
Microenvironmental alterations, including erythroblastic island prominence, are highlighted as underutilized diagnostic parameters.
These findings are presented across five cases to demonstrate a 'structured, contextual morphological approach' as complementary to immunophenotypic and molecular techniques.
Chiriac R, Leparc M, Stanescu M, Mery L, Milandri J, Jaillard M, et al.. (2026). Hidden morphological clues in deceptive bone marrow pathologies.. Annales de biologie clinique. https://doi.org/10.1684/abc.2026.2027