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Waldenstrom's Macroglobulinemia 1 ¿¹ A Case of Waldenstrom's Macroglobulinemia

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Abstract

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The Waldenstrom's macroglobulinemia is a slow growing progressive malignant
lymphoproliferative disorder and charaterized by macroglobulin(Ig M) paraprotein 'spike'
on the serum protein electrophoresis associated with bone marrow proliferation of
plasmacytoid lymphocyte. The age at diagnosis of patient is ranging from 4th to 9th
decade and the peak age is 6th to 7th decade. The major criteria for diagnosis are a
monoclonal Ig M serum protein abnormality present in concentrations greater than 1 g/dl
and clinical manifestations included weight loss, bleeding tendency, presence of abnormal
masses ,lymphadenopathy ,hepatosplenomegaly, central and peripheral neuropathy and
hyperviscosity syndrome may develop as a complication of macroglobulinemia. We
experienced one case of Waldenstrom's macroglobulinemia, 68-year-old woman, who
visited our hospital due to slow growing multiple cervical masses. On physical
examination, painless cervical, axillary and inguinal lymphadenopathy, and hepatomegaly
were noted. The hematological study showed moderate degree of normocytic
normochromic anemia. The serum protein elect trophoresis showed typical monoclonal
gammopathy. The serum protein immunoelectrophoresis revealed Ig M-lambda type
M-protein. Concentration of Is M was 3.04 g/dl. Bone marrow aspiration findings were
nonspecific except slightly increase of plasma cells. The findings of bone marrow and
lymph node biopsies showed no evidence of malignancy as lymphoma or leukemia. The
peroxidase antiperoxidase (PAP) and methyl green pyronine stains of bone marrow and
lymph node also showed non-specific findings. The B-lymphocyte count of the
peripheral blood by immunoflurorescent method revealed markedly increased subsets
along with the increased total B-cell counts.

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