Solitary plasmacytoma of bone--a rare disorder with an unusual evolution

Postgrad Med J. 1993 Feb;69(808):153-4. doi: 10.1136/pgmj.69.808.153.

Abstract

A 40 year old woman presented with a spinal epidural tumour, which on histology was shown to be a plasmacytoma. At that time she had no evidence of multiple myeloma. Ten months later, she developed a second isolated plasmacytoma in the spleen, for which she underwent splenectomy. Two years after her initial presentation she had another recurrence in the liver, followed by a full-blown picture of multiple myeloma. The myeloma was progressive and resistant to all forms of chemotherapy. She finally died of a massive gastrointestinal haemorrhage. The clinical features, natural evolution and management of solitary plasmacytomas are discussed.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Combined Modality Therapy
  • Etoposide / therapeutic use
  • Female
  • Follow-Up Studies
  • Humans
  • Liver Neoplasms / drug therapy
  • Liver Neoplasms / secondary
  • Multiple Myeloma / drug therapy
  • Plasmacytoma / drug therapy
  • Plasmacytoma / surgery*
  • Spinal Neoplasms / surgery*
  • Splenectomy
  • Splenic Neoplasms / secondary
  • Splenic Neoplasms / surgery
  • Vincristine / therapeutic use

Substances

  • Vincristine
  • Etoposide