Abstract

Solid pseudopapillary neoplasm of the pancreas (SPNP) is a rare primary neoplasm with distinct clinicopathological features. The tumor most commonly occurs inyounger (premenopausal) women and is typified by low malignant potential and an excellent overall prognosis. A retrospective search over 20 years at two referral tertiary care institutions (King Faisal Hospital and Research Center andKing Abdulaziz University Hospital, Jeddah, Kingdom of Saudi Arabia)revealed 12 female patients diagnosed with SPNPs. The reslts of ancillary studies performed at the time of diagnosis were also reviewed and placed in the context of current recommendations. The clinical and pathological findings were reviewed. All patients were females, aged 18 to 30 years. Eight patients presented with abdominal pain, of which two experienced significant weight loss, and four presented with abdominal mass/discomfort. The tumor size ranged from 1.5 and 15 cm. Two cases were initially diagnosed as neuroendocrine tumors (NETs). One of the cases presented as a multifocal disease. All patients were treated surgically with a follow-up period between one and 11 years. Only one patient presented with peritoneal metastasis after seven years of follow-up, but generally, all are doing well. We have analyzed 12 SPNP cases in our population over 20 years (2001-2021) in this study. In brief, SPNP is a low-grade malignant potential tumor. Even though SPNP is a recognized entity, diagnostic challenges can ariseparticularly in the setting of limited sampling.Pathologists must be aware of the classic morphological features of SPNP and the characteristic profile of immunohistochemistryand be able to differentiate SPNP from other mimickers, especially well-differentiated NETs of the pancreas, andultimately to avoid misdiagnosis and unnecessary oncologic treatment. Adequate surgical resection with negative margins is associated with an excellent outcome.

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