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• W2800966474 abstract "Signet ring cell carcinoma (SRCC) of the ampulla of Vater is an extremely rare tumor. Our case describes a 45-year-old female presenting with jaundice and pruritus. Computed tomography, endoscopy, and endoscopic retrograde cholangiopancreatography showed a tumor of the ampulla of Vater without distant metastasis. Histological biopsy confirmed a malignant tumor with SRCC characteristics and immunohistochemical staining revealed a mixed type profile (both intestinal and pancreatobiliary characteristics). A pylorus-preserving pancreatoduodenectomy was performed and the patient recovered without complications. Pathology results concluded a pT2N0 ampullary SRCC. SRCC of the ampulla of Vater is known to be highly malignant. After 13 months of follow-up, our patient showed no signs of recurrence." @default.
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• W2800966474 date "2018-04-27" @default.
• W2800966474 modified "2023-10-16" @default.
• W2800966474 title "Signet Ring Cell Carcinoma of the Ampulla of Vater: A Rare Histopathological Variant" @default.
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• W2800966474 doi "https://doi.org/10.1159/000488903" @default.
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