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Published on: November 8, 2011
Polyclonal B-cell lymphocytosis mimicking malignant lymphoma in a newborn
Kit Fai Wong1, Hui Leung Yuen, Jennifer N S Leung
1Department of Pathology, Queen Elizabeth Hospital, Hong Kong SAR, China. kfwong@ha.org.hk <kfwong@ha.org.hk>
Insights
A newborn experienced fever and unusual lymphocytes, initially suspected as lymphoma. Further tests revealed a benign, self-limiting polyclonal lymphocytosis, resolving within a month.
Area of Science:
- Pediatric Hematology
- Immunology
- Neonatal Medicine
Background:
- Neonatal fever and lymphocytosis can mimic serious conditions like leukemia.
- Distinguishing benign reactive lymphocytosis from malignancy is crucial in newborns.
Observation:
- A 17-day-old infant presented with fever and atypical peripheral blood lymphocytes.
- These lymphocytes exhibited large size, irregular nuclei, and immature features, raising concern for malignant lymphoma.
- Initial presentation suggested a potential leukemic phase of lymphoma.
Findings:
- Immunophenotyping identified the lymphocytes as CD19-positive B cells expressing both kappa and lambda light chains.
- Molecular studies confirmed a polyclonal immunoglobulin heavy-chain gene rearrangement, indicating a non-clonal origin.
- Cytogenetic analysis revealed a normal karyotype, and infectious workup was negative.
Implications:
- This case highlights the importance of comprehensive immunophenotypic and molecular analysis in diagnosing neonatal lymphocytosis.
- It demonstrates that unusual lymphocyte morphology in neonates can represent a benign, self-limiting condition.
- Accurate diagnosis prevents unnecessary aggressive treatment for conditions like lymphoma.
Abstract:
We describe a 17-day-old newborn with fever and peripheral blood lymphocytosis. The circulating lymphocytes were large with lobulated and nucleolated nuclei. Their immature and uniform appearance raised the possibility of malignant lymphoma in the leukemic phase. Immunophenotypic study, however, showed that the lymphocytes were CD19(+) B cells with expression of both kappa and lambda light chains. Molecular biology study confirmed a polyclonal nature of the immunoglobulin heavy-chain gene. Cytogenetic analysis showed a normal karyotype, and viral cultures and serologic studies yielded negative results. The polyclonal lymphocytosis was self-limiting and disappeared within a month.
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