Immunoproliferative small intestinal disease with protein loss complicated with duodenal T cell lymphoma during progression

Intern Med. 2008;47(4):299-303. doi: 10.2169/internalmedicine.47.0524. Epub 2008 Feb 15.

Abstract

A 52-year-old man was admitted to our hospital in October 2001 with abdominal pain. Abdominal X-ray indicated a diagnosis of ileus. Histopathological and immunological examination resulted in a diagnosis of immunoproliferative small intestinal disease (IPSID). He was treated with THP-COP therapy (pirarubicin, cyclophosphamide, vincristine, and prednisolone), which resulted in complete remission. Outpatient follow-up revealed hypoalbuminemia in May 2003 and upper gastrointestinal endoscopy showed duodenal mucosal nodularity. He was diagnosed with relapsed IPSID and salvage chemotherapy was started. Follow-up endoscopy confirmed that the therapy was effective, but uncovered another duodenal mucosal nodularity. Immunohistochemical staining revealed T-cell lymphoma. Chemotherapy was discontinued and the patient died in December 2004.

Publication types

  • Case Reports

MeSH terms

  • Disease Progression
  • Duodenal Neoplasms / etiology*
  • Fatal Outcome
  • Humans
  • Immunoproliferative Small Intestinal Disease / complications*
  • Immunoproliferative Small Intestinal Disease / metabolism
  • Lymphoma, T-Cell / etiology*
  • Male
  • Middle Aged
  • Proteins / metabolism

Substances

  • Proteins