World Journal of Surgical Oncology (Nov 2007)

Castleman's disease in the head of the pancreas: report of a rare clinical entity and current perspective on diagnosis, treatment, and outcome

  • Ghosh Bimal C,
  • Desoto-Lapaix Fidelina,
  • Zenilman Michael E,
  • Wieczorek Rosemary L,
  • Wang Hongbei,
  • Bowne Wilbur B

DOI
https://doi.org/10.1186/1477-7819-5-133
Journal volume & issue
Vol. 5, no. 1
p. 133

Abstract

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Abstract Background Castleman's disease of the pancreas is a very rare condition that may resemble more common disease entities as well as pancreatic cancer. Case presentation Here we report the case of a 58-year-old African American male with an incidentally discovered lesion in the head of the pancreas. The specimen from his pancreaticoduodectomy contained a protuberant, encapsulated mass, exhibiting microscopic features most consistent with localized/unicentric Castleman's disease. These included florid follicular hyperplasia with mantle/marginal zone hyperplasia along with focal progressive transformation of germinal centers admixed with involuted germinal centers. Conclusion To date, eight cases of Castleman's disease associated with the pancreas have been described in the world literature. We report the first case of unicentric disease situated within the head of the pancreas. In addition, we discuss the diagnostic dilemma Castleman's disease may present to the pancreatic surgeon and review current data on pathogenesis, treatment, and outcome.