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Precursor B lymphoblastic lymphoma presenting as lytic bone lesions.
S Iravani1, T P Singleton, C W Ross
1Department of Pathology, University of Michigan Medical School, Ann Arbor 48109-0602, USA.
American Journal of Clinical Pathology
|December 10, 1999
Summary
Precursor B lymphoblastic lymphoma can present as bone lesions without bone marrow involvement. Immunophenotyping is crucial for diagnosing this aggressive yet curable lymphoma.
Area of Science:
- Hematology
- Oncology
- Pathology
Background:
- Precursor B lymphoblastic lymphoma (B-LL) is an aggressive hematologic malignancy.
- B-LL commonly affects skin and lymph nodes, but can present as lytic bone lesions.
- Differential diagnosis in bone includes small round blue cell tumors, diffuse large B-cell lymphoma, and acute myelogenous leukemia.
Purpose of the Study:
- To describe the morphologic and immunophenotypic characteristics of B-LL presenting with bone lesions.
- To highlight the importance of immunophenotyping for accurate diagnosis.
Main Methods:
- Retrospective analysis of 4 patients (2 children, 1 teen, 1 adult) with bone pain and osteolytic lesions.
- Morphologic assessment and immunohistochemical staining of neoplastic cells.
- Panel of antibodies included CD10, CD20, CD34, CD43, CD45/CD45RB, CD79a, CD99 (MIC2), and terminal deoxynucleotidyl transferase (TdT).
Main Results:
- All 4 patients presented with bone pain and osteolytic lesions, without peripheral blood or iliac bone marrow involvement.
- Immunohistochemical staining revealed positivity for CD43 (4/4) and TdT (4/4).
- Additional markers showed heterogeneity: CD10 (3/4), CD20 (3/4), CD34 (1/4), CD45/CD45RB (2/4), CD79a (4/4), CD99 (MIC2) (2/4). CD3 was negative in all cases.
Conclusions:
- Precursor B lymphoblastic lymphoma can manifest primarily in bone with osteolytic lesions.
- Immunophenotypic heterogeneity necessitates a comprehensive antibody panel for accurate diagnosis.
- Timely diagnosis through immunophenotyping is essential for effective treatment of this curable malignancy.