Abstract
BackgroundIntraductal tubulopapillary neoplasm (ITPN) is a rare pancreatic intraductal neoplasm. It is characterized by a tubulopapillary growth pattern, entirely high-grade atypical cells, minimal cytoplasmic mucin, and no obvious luminal mucin secretion. Most of its biological nature remains unclear.Case presentationWe herein report a case of intrapancreatic recurrence of ITPN in the remnant pancreas of a patient who underwent pancreatoduodenectomy 16 years previously for a noninvasive intraductal pancreatic head tumor. We reexamined the primary tumor and compared it with the most recently resected specimen. Histologically, the primary tumor showed a tubulopapillary growth of high-grade atypical cells with scanty cytoplasmic mucin, which was similar to the recently resected specimen except for the invasive area. Immunohistochemically, the neoplastic cells in both specimens showed focal staining of MUC1 and positivity for MUC6 but negativity for MUC2, MUC5AC, CDX2, and trypsin. Molecular analysis revealed no KRAS/GNAS/BRAF/PIK3CA mutations in either of the specimens.ConclusionsThese findings of the original tumor and recently resected tumor were compatible with the features of ITPN. Thus, recurrence is possible even for a primary noninvasive ITPN, and long-term surveillance is recommended.
Highlights
Intraductal tubulopapillary neoplasm (ITPN) is a rare pancreatic intraductal neoplasm
According to the 2010 World Health Organization (WHO) classification [1], pancreatic intraductal neoplasms are divided into intraductal papillary mucinous neoplasm (IPMN) and ITPN
We investigated the KRAS/BRAF/GNAS/ PIK3CA mutational status of the original tumor and the recently resected tumors from the pancreatic body and tail. These analyses revealed no KRAS/BRAF/GNAS/PIK3CA mutations in all tumor samples
Summary
We experienced a case of a recurrent ITPN with an invasive component after a 16-year interval from the initial surgery of a noninvasive ITPN.
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