Abstract |
A 39-year-old male was referred to our hospital in June, 1993, because of leukocytosis. Physical examinations showed massive splenomegaly without any lymphadenopathy. The white blood cell count was 13,800/microliters with 87% morphologically mature lymphocytes. Bone marrow aspirate revealed hypercellularity with 67% lymphocytes morphologically similar to peripheral lymphocytes. The lymphocytes displayed monoclonal rearrangements of immunoglobulin genes and the phenotype of CD5-CD19+CD20+ CD21+ and Smlg+. Splenectomy was effective against neutropenia and thromboytopenia. The clinical and laboratory findings of this case were unusual compared to those of typical B-CLL in massive splenomegaly, no lymphadenopathy and CD5-phenotype, suggesting the heterogeneity of B-CLL.
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Authors | T Yamada, H Ninomiya, T Horiuchi, K Takada, T Hato, K Yamauchi, M Yasukawa, S Fujita |
Journal | [Rinsho ketsueki] The Japanese journal of clinical hematology
(Rinsho Ketsueki)
Vol. 36
Issue 10
Pg. 1230-2
(Oct 1995)
ISSN: 0485-1439 [Print] Japan |
PMID | 8531336
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- CD5 Antigens
- Immunoglobulins
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Topics |
- Adult
- CD5 Antigens
(immunology)
- Gene Rearrangement
- Humans
- Immunoglobulins
(genetics)
- Leukemia, Lymphocytic, Chronic, B-Cell
(complications, genetics, immunology)
- Lymphatic Diseases
- Male
- Splenomegaly
(complications, surgery)
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