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Published on: April 16, 2019
[T-cell type non-Hodgkin's lymphoma associated with eosinophilia]
M Matsuzaki1, Y Shimamoto, T Tokioka
1Department of Internal Medicine, Saga Medical School.
Insights
This study reports a rare case of non-Hodgkin's lymphoma presenting with severe hypereosinophilia. Chemotherapy effectively resolved both the lymphoma and the eosinophilia, suggesting a potential link.
Area of Science:
- Hematology
- Oncology
Background:
- Non-Hodgkin's lymphoma (NHL) is a diverse group of lymphoid malignancies.
- Hypereosinophilia, characterized by elevated eosinophil counts, can be associated with various conditions, including malignancies.
Observation:
- A 65-year-old male presented with generalized lymphadenopathy and marked leukocytosis (40,900/microliters) with 88% eosinophils.
- Bone marrow examination revealed increased eosinophils and precursors without other abnormalities.
- Biopsy confirmed diffuse, medium-sized cell non-Hodgkin's lymphoma with lymphoma cell infiltration in the stomach.
Findings:
- Extensive investigations failed to identify an etiology for the patient's hypereosinophilia.
- Combination chemotherapy led to a dramatic resolution of both the eosinophilia and lymphadenopathy.
- The patient's marker analysis was CD3+4+8-, and human T-lymphotropic virus type I antibody was negative.
Implications:
- This case highlights the unusual association between hypereosinophilia and non-Hodgkin's lymphoma.
- It suggests that lymphoma should be considered in the differential diagnosis of unexplained hypereosinophilia.
- The prompt response to chemotherapy indicates a potential paraneoplastic or direct effect of the lymphoma on eosinophil production.
Abstract:
A 65-year-old man was admitted to our hospital in January 1990, because of weakness of upper limbs. On admission he was found to have generalized lymphadenopathy and leukocytosis. His WBC count was 40,900/microliters with 88% eosinophils. The bone marrow showed an increased number of eosinophils and their precursors but no other abnormalities. A diagnosis of non-Hodgkin's lymphoma (diffuse, medium sized cell type) was made by biopsy of his inguinal lymph node. The result of marker analysis was consistent with CD3+4+8-. The antibody to human T-lymphotropic virus type I was negative. A stomach biopsy revealed lymphoma cell infiltration. Extensive studies to identify the cause of the eosinophilia were undertaken, with consistently negative results. Combination chemotherapy was begun, and resulted in a dramatic resolution of the eosinophilia and the lymphadenopathy. The association of hypereosinophilia with non-Hodgkin's lymphoma is unusual. We report a patient with eosinophilia and non-Hodgkin's lymphoma, and discussed its possible etiology.
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