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Marked splenomegaly, an unusual initial symptom of myeloma, was observed in two patients. The exact cause of spleen enlargement in these cases remains unclear despite investigations.

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Area of Science:

  • Hematology
  • Oncology
  • Pathology

Background:

  • Multiple myeloma commonly causes skeletal damage, anemia, and renal failure.
  • Splenomegaly is a rare presenting symptom of myeloma, with its pathophysiology often unclear.

Purpose of the Study:

  • To report two unique cases of myeloma presenting with significant splenomegaly as the initial symptom.
  • To investigate the underlying pathology of splenomegaly in these myeloma patients.

Main Methods:

  • Case report of two patients with myeloma and marked splenomegaly.
  • Histopathological examination of spleen tissue post-splenectomy.
  • Immunohistochemical analysis to identify plasma cell infiltration.

Main Results:

  • Both patients presented with severe splenomegaly causing pain and infarction, necessitating splenectomy.
  • Histology revealed sinus lining cell proliferation with IgA paraprotein in one case and red pulp expansion in the other.
  • Plasma cell infiltration of the spleen was not confirmed despite unusual morphology in peripheral blood and marrow.

Conclusions:

  • Splenomegaly can be an unusual initial presentation of myeloma.
  • The pathophysiology of splenomegaly in these cases remains obscure and requires further investigation.
  • These cases highlight the diverse and sometimes atypical manifestations of multiple myeloma.