| Literature DB >> 12512840 |
Tetsuaki Sekikawa1, Shinobu Takahara, Takeshi Kawano, Shuji Nakada, Kiyoshi Ito, Satsuki Iwase, Hisashi Yamada, Masayuki Kobayashi, Junko Horiguchi-Yamada.
Abstract
B-cell diseases are classified on the basis of the normal differentiation stages. We report here a case of a patient with a long history of leukocytosis, splenomegaly without lymphadenopathy, and hyperviscosity symptoms. Clinically, the patient's diagnosis was leukemic Waldenstrom macroglobulinemia. Chromosomal analysis revealed translocation t(2;7)(p11;q22) along with disease progression. Death occurred from pulmonary infection at 46 months after the initial presentation. At autopsy, malignant lymphocytes were found in the marginal areas of the spleen with spreading to the bone marrow and the liver. The histologic findings were consistent with splenic marginal zone lymphoma. We examined the sequences of the immunoglobulin V(H) gene in cells from the initial peripheral blood and from the spleen at autopsy and found that the sequences were identical and had no somatic hypermutation. Macroglobulinemia can occur in various B-cell disorders, including splenic marginal zone lymphoma, even with the transformation of unmutated B-lymphocytes.Entities:
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Year: 2002 PMID: 12512840 DOI: 10.1007/bf02982811
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490