1. REACTIVE PLASMACYTOSIS AT THE ONSET OF ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA. CASE REPORT
- Author
-
N. G. Chernova, M. N. Sinitsyna, A. M. Kovrigina, Y. V. Sidorova, I. V. Galtseva, S. A. Mar’ina, V. N. Dvirnyk, and E. E. Zvonkov
- Subjects
angioimmunoblastic t-cell lymphoma ,Plasma cell leukemia ,Angioimmunoblastic T-cell lymphoma ,Pathology ,medicine.medical_specialty ,medicine.diagnostic_test ,business.industry ,Plasmacytosis ,Lymph node biopsy ,Hematology ,medicine.disease ,Lymphoma ,multiple myeloma ,Immunophenotyping ,medicine.anatomical_structure ,Oncology ,reactive plasmacytosis ,hemic and lymphatic diseases ,Medicine ,Diseases of the blood and blood-forming organs ,plasma-cell leukemia ,Bone marrow ,RC633-647.5 ,business ,Generalized lymphadenopathy - Abstract
Angioimmunoblastic T-cell lymphoma is a rare T-cell lymphoproliferative disease with generalized lymphadenopathy, hepatosplenomegaly, intoxication and polyclonal hypergammaglobulinemia. The persistence of plasma cells in peripheral blood can be a manifestation of both tumor and reactive processes. In our article, we described the case of angioimmunoblastic T-cell lymphoma with an increase in the number of peripheral blood plasma cells to 28 %, and in bone marrow to 9 %. The complex diagnostics, including plasma cells immunophenotyping, morphology of the lymph node biopsy and bone marrow samples, made it possible to verify the diagnosis of angioimmunoblastic T-cell lymphoma with polyclonal plasmacytosis.
- Published
- 2018
- Full Text
- View/download PDF