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Sclerotic marginal zone lymphoma: A case report.
Zade Moureiden1, Hammad Tashkandi1, Mohammad Omar Hussaini2
1Pathology and Laboratory Medicine, Moffitt Cancer Center, Tampa, FL 33612, United States.
A rare sclerotic variant of marginal zone lymphoma (MZL), an indolent non-Hodgkin B cell lymphoma, was identified. This case highlights a new architectural pattern and potential diagnostic pitfall in lymphoma diagnosis.
Area of Science:
- Hematology
- Oncology
- Pathology
Background:
- Marginal zone lymphoma (MZL) is an indolent non-Hodgkin B cell lymphoma.
- MZL presents with various architectural patterns, but a sclerotic variant has not been previously reported.
- This sclerotic variant can be a diagnostic pitfall.
Observation:
- A 66-year-old male presented with left upper extremity swelling due to a large axillary mass.
- Initial needle core biopsy showed sclerotic tissue with atypical B lymphoid infiltrate, proving non-diagnostic.
- Excisional biopsy revealed extensive fibrosis with a minor component of infiltrating B cells, confirmed as MZL by flow cytometry and gene rearrangement studies.
Findings:
- The patient was diagnosed with marginal zone lymphoma (MZL).
- The lymphoma exhibited an unusual sclerotic architectural pattern characterized by extensive fibrosis.
- Immunophenotyping and molecular studies confirmed a clonal B cell population.
Implications:
- This case report describes a novel sclerotic architectural pattern of marginal zone lymphoma.
- The sclerotic presentation can be mistaken for non-specific fibrosis, posing a significant diagnostic challenge.
- Recognition of this pattern is crucial for accurate diagnosis and appropriate management of MZL.
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