Related Experiment Video
Updated: Aug 9, 2026

A Detailed Protocol for Characterizing the Murine C1498 Cell Line and its Associated Leukemia Mouse Model
Published on: October 14, 2016
Hairy cell leukemia variant with features of intrasinusoidal bone marrow involvement
Charin Ya-In1, Joseph Brandwein, Dominic Pantalony
1Department of Laboratory Hematology, Princess Margaret Hospital/University Health Network, University of Toronto, Toronto, Ontario, Canada.
Insights
Hairy cell leukemia variant (HCL-V) presents atypically with intrasinusoidal bone marrow infiltration. This case highlights the importance of integrating all diagnostic data for accurate HCL-V diagnosis.
Area of Science:
- Hematology
- Oncology
- Pathology
Background:
- Hairy cell leukemia variant (HCL-V) is a rare lymphoproliferative neoplasm.
- Typical HCL-V bone marrow involvement shows interstitial or diffuse infiltration.
Observation:
- A case of HCL-V with an unusual intrasinusoidal bone marrow infiltration pattern is presented.
- Peripheral blood and bone marrow aspirates revealed abnormal lymphoid cells with cytoplasmic projections, weakly tartrate-resistant acid phosphatase (TRAP)-positive.
- Immunostaining confirmed CD20 positivity within bone marrow sinusoids and weak DBA44 positivity.
Findings:
- Flow cytometry showed cells positive for CD19, CD20, CD11c, CD103, and lambda light chain restriction, but negative for CD25.
- Splenic red pulp infiltration was observed, characteristic of HCL/HCL-V, distinguishing it from splenic lymphoma with villous lymphocytes (SLVL) or splenic marginal zone lymphoma (SMZL).
Implications:
- This case demonstrates an atypical bone marrow presentation of HCL-V.
- Accurate diagnosis requires correlation of clinical, peripheral blood, bone marrow biopsy, and spleen pathology findings.
Abstract:
Hairy cell leukemia variant (HCL-V) is a rare lymphoproliferative disorder. We report a case of HCL-V with an intrasinusoidal pattern of bone marrow involvement without interstitial or diffuse infiltration that is typical of HCL and its variant. The peripheral blood and bone marrow aspirates demonstrated abnormal lymphoid cells with cytoplasmic projections that were weakly positive for tartrate-resistant acid phosphatase cytochemical staining. Immunostaining of the bone marrow biopsy specimen showed that these cells were strongly positive for CD20, located within bone marrow sinusoids, and weakly positive for DBA44. By flow cytometry, these cells were positive for CD19, CD20, CD11c, and CD103, exhibited lambda light chain restriction, and were negative for CD25. The patient was initially diagnosed as having splenic lymphoma with villous lymphocytes (SLVL) or splenic marginal zone lymphoma (SMZL) (World Health Organization designation) and treated with fludarabine followed by splenectomy with simultaneous liver biopsy. The pathologic analysis of the spleen revealed infiltration of red pulp by the critical cells without white pulp involvement, which is characteristic of HCL and HCL-V but not of SLVL (SMZL). This case illustrates an atypical marrow presentation of HCL-V and emphasizes the need to correlate all clinical and pathologic data, including tissue biopsy, in reaching a diagnosis.

