Journal of Medical Case Reports (Dec 2018)

Secondary extramedullary plasmacytoma of sigmoid colon in a patient with multiple myeloma: a case report

  • Dimitris Fagkrezos,
  • Konstantinos Manes,
  • Konstantina Paraskeva,
  • Michalis Lenos,
  • Charikleia Triantopoulou,
  • Dimitra Apessou,
  • Petros Maniatis

DOI
https://doi.org/10.1186/s13256-018-1888-4
Journal volume & issue
Vol. 12, no. 1
pp. 1 – 7

Abstract

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Abstract Background Extramedullary plasmacytoma is an uncommon tumor that most often involves the nasopharynx or upper respiratory tract. Extramedullary plasmacytoma is a type of plasma cell neoplasm that can present as a primary tumor or secondary to another plasma cell neoplasm, such as multiple myeloma. Secondary extramedullary plasmacytoma is usually noted in the advanced stages of the disease. Involvement of the gastrointestinal tract occurs in approximately 10% of cases. Case presentation A 71-year-old Caucasian woman with known diverticular disease of the colon and multiple myeloma diagnosed 3 years previously, with monoclonal bands of immunoglobulin A, lambda light chains, and multiple osteolytic lesions, presented to our hospital with abdominal pain, abdominal discomfort, and pneumoperitoneum. She underwent left colectomy for diverticulitis with perforation, and an extramedullary secondary colonic plasmacytoma was found in histopathological examination of the sigmoid colon. Conclusions Plasmacytoma is known to occur in extraosseous sites. The stomach and small intestine are the most commonly involved sites in the gastrointestinal tract. Secondary extramedullary plasmacytoma of the colon is rare. Colonic plasmacytoma may have varying clinical presentations, such as inflammatory bowel disease and multiple colonic strictures. Although these cases are rare, treating physicians as well as radiologists, pathologists, and surgeons should be aware of this entity.

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