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Article Abstract

Rationale: Solid pseudopapillary neoplasm of the pancreas, first classified as a malignant epithelial tumor of the pancreas in 2019, is rare and usually occurs in young women, with a high incidence at approximately 30 years of age. Herein, we present a case of solid pseudopapillary neoplasm of the pancreas with elevated β-human chorionic gonadotropin (HCG) levels, which, to our knowledge, has not been reported in the literature.

Patient Concerns: A 35-year-old woman of childbearing age presented with a chief complaint of vaginal bleeding and was admitted to our hospital. Her β-HCG level was elevated; however, a complete endometrial biopsy and related imaging examinations revealed no evidence of pregnancy or trophoblastic neoplasm. Computed tomography revealed a lump of abnormal signals in the head of the pancreas, which was suspected to be a solid pseudopapilloma.

Diagnoses: Hence, surgery was performed, and the postoperative pathological diagnosis of a solid pseudopapillary neoplasm of the pancreas was confirmed.

Interventions And Outcomes: The tumor was completely removed by surgery. Notably, the patient's β-HCG level gradually decreased after removal of the pancreatic mass and returned to normal levels after 1 month.

Lessons: We present a case of solid pseudopapillary neoplasm of the pancreas that was diagnosed using hematoxylin and eosin staining and immunohistochemistry. In our case, the solid pseudopapillary neoplasm partially expressed β-HCG. Further studies are needed to confirm whether β-HCG promotes the occurrence and development of solid pancreatic pseudopapillary neoplasms.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12385044PMC
http://dx.doi.org/10.1097/MD.0000000000043808DOI Listing

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