Classical type and blastoid variant mantle cell lymphoma in the same lymph node: Histology and cytological findings

Shin-Ichi Nakatsuka1, Tadasuke Nagatomo2,3, Teruaki Nagano1

  • 1Department of Pathology, Kansai Rosai Hospital, Amagasaki, Hyogo, 660-8511, Japan.

Diagnostic Cytopathology
|February 1, 2017
PubMed

Insights

This study presents a rare case of mantle cell lymphoma (MCL) showing a direct histological transition from classical MCL (C-MCL) to the aggressive blastoid variant (BV-MCL) within the same lymph node, suggesting a potential pathogenetic link.

Area of Science:

  • Hematopathology
  • Oncology
  • Cellular Biology

Background:

  • Mantle cell lymphoma (MCL) is a B-cell non-Hodgkin lymphoma.
  • Blastoid variant MCL (BV-MCL) represents an aggressive subtype characterized by blastic morphology.
  • Transformation from classical MCL (C-MCL) to aggressive variants is known, but simultaneous presence in one specimen is rare.

Observation:

  • A 53-year-old male presented with a submandibular tumor.
  • Cytology showed a proliferation of large blastic lymphoid cells.
  • Histology revealed a lymph node with distinct areas of C-MCL and BV-MCL.

Findings:

  • Immunohistochemistry confirmed both components as CD5(+), CD10(-), CD20(+), cyclin D1(+), and SOX11(+).
  • Fluorescent in situ hybridization identified the characteristic IgH/BCL1 translocation in both cell populations.
  • The diagnosis was BV-MCL with coexistent C-MCL.

Implications:

  • This case provides evidence for a direct histopathological transition from C-MCL to BV-MCL within a single lesion.
  • Accurate identification of BV-MCL is crucial for prognostication and treatment planning.
  • Utilizing ancillary diagnostic tools is recommended for suspected BV-MCL cases.