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CASE REPORT
Primary gastric plasmacytoma: a rare entity
  1. Rui Caetano Oliveira1,
  2. Pedro Amaro2,
  3. Maria José Julião1,
  4. Maria Augusta Cipriano3
  1. 1Department of Pathology, Hospitais da Universidade de Coimbra, Coimbra, Portugal
  2. 2Department of Gastroenterology, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal
  3. 3Pathology Department, University Hospital Center of Coimbra, Coimbra, Portugal
  1. Correspondence to Dr Rui Caetano Oliveira, ruipedrocoliveira{at}hotmail.com

Summary

Extramedullary plasmacytomas (EP) are tumours composed by a monoclonal population of plasma cells that arise in extraosseus tissues, comprising <5% of all plasma cell neoplasms. Usually, EP arise in the head and neck region, and the stomach is the second most common location—gastric plasmacytoma (GP). Clinical and radiological manifestations are unspecific and may mimic other tumours like gastric adenocarcinomas, gastric stromal tumours and lymphomas, mainly marginal cell lymphoma (MALT lymphoma) and usually definitive diagnosis is provided by pathological evaluation. We present a case of primary GP, discovered incidentally as a polypoid lesion. Tumour was composed by sheets of mature and immature plasmocytes positive for CD138 on immunohistochemistry, without Helicobacter pylori identification. The patient is alive 6 years later and without tumour relapse.

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Footnotes

  • Contributors RCO, PA, MJJ and MAC are responsible for conception and design or acquisition of data or analysis and interpretation of data; drafting the article or revising it critically for important intellectual content; and final approval of the version to be published.

  • Competing interests None declared.

  • Patient consent Obtained.

  • Provenance and peer review Not commissioned; externally peer reviewed.