S6070 A Case of Intense Pruritus in the Setting of Invasive Mucinous Adenocarcinoma of the Ampulla of Vater

Introduction: Ampullary cancer, a rare form of cancer that originates from the ampulla of Vater, is a unique condition, accounting for only 0.2% of gastrointestinal cancers. We discuss a case of a patient who, despite the rarity of this cancer, presented to the emergency department with intense pruritus and was found to have invasive mucinous adenocarcinoma of the ampulla, leading to biliary and pancreatic duct obstruction. Case Description/Methods: A 62-year-old woman with a history of coronary artery disease status post CABG and a remote history of tobacco and alcohol use presented with complaints of nausea, vomiting, abdominal pain, dark urine, jaundice, and 20 lbs of weight loss over the past year. Full-body intense pruritus prompted her to come to the emergency department. Computed tomography scan of the abdomen/pelvis with contrast showed 3 × 1.3 × 2.4 cm low attenuation neoplasm at the pancreatic head and ampulla, resulting in an abrupt cut off of the common bile and pancreatic duct. Labs were notable for elevated liver enzymes, alkaline phosphatase, and direct bilirubin. Her CA 19-9 was 37, and CEA was 3.1. GI was consulted for esophagogastroduodenoscopy and EUS with biopsy. Surgery and oncology were consulted after the biopsy revealed invasive adenocarcinoma in the pancreatic head and adenomatous epithelium with high-grade dysplasia from the ampulla of Vater. She subsequently underwent ERCP with stent placement and pancreaticoduodenectomy. Whipple pathology showed invasive mucinous adenocarcinoma arising from the duodenum, invading through the muscularis propria and into the adjacent pancreatic head. Our patient with pT4pN0 stage 2 malignancy was safely discharged 11 days after admission a with resolution of most of her initial symptoms. Discussion: Our patient initially experienced emotional distress and was reluctant to undergo diagnostic testing. The value of a multidisciplinary team in providing comprehensive care and patient support, along with the crucial role of empathetic communication, was learned. These factors ultimately led our patient to agree to a biopsy and Whipple procedure, which significantly improved her pruritus. Further outpatient workup consists of a computed tomography scan of the chest, an outpatient PET scan, and obtaining circulating tumor DNA. Oncology recommended testing for microsatellite instability/ mismatch repair deficiency to be assessed on the tumor; if testing is positive, adjuvant chemotherapy with either FOLFOX or CAPOX was discussed. Since being discharged, our patient has followed up with surgery and is due to follow up with oncology.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001152740.34095.d6
Primary Topic
Pancreatic and Hepatic Oncology Research
Type
article
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article

S6070 A Case of Intense Pruritus in the Setting of Invasive Mucinous Adenocarcinoma of the Ampulla of Vater

The American Journal of Gastroenterology
Pancreatic and Hepatic Oncology Research
article

S6070 A Case of Intense Pruritus in the Setting of Invasive Mucinous Adenocarcinoma of the Ampulla of Vater

article en

Abstract

Introduction: Ampullary cancer, a rare form of cancer that originates from the ampulla of Vater, is a unique condition, accounting for only 0.2% of gastrointestinal cancers. We discuss a case of a patient who, despite the rarity of this cancer, presented to the emergency department with intense pruritus and was found to have invasive mucinous adenocarcinoma of the ampulla, leading to biliary and pancreatic duct obstruction. Case Description/Methods: A 62-year-old woman with a history of coronary artery disease status post CABG and a remote history of tobacco and alcohol use presented with complaints of nausea, vomiting, abdominal pain, dark urine, jaundice, and 20 lbs of weight loss over the past year. Full-body intense pruritus prompted her to come to the emergency department. Computed tomography scan of the abdomen/pelvis with contrast showed 3 × 1.3 × 2.4 cm low attenuation neoplasm at the pancreatic head and ampulla, resulting in an abrupt cut off of the common bile and pancreatic duct. Labs were notable for elevated liver enzymes, alkaline phosphatase, and direct bilirubin. Her CA 19-9 was 37, and CEA was 3.1. GI was consulted for esophagogastroduodenoscopy and EUS with biopsy. Surgery and oncology were consulted after the biopsy revealed invasive adenocarcinoma in the pancreatic head and adenomatous epithelium with high-grade dysplasia from the ampulla of Vater. She subsequently underwent ERCP with stent placement and pancreaticoduodenectomy. Whipple pathology showed invasive mucinous adenocarcinoma arising from the duodenum, invading through the muscularis propria and into the adjacent pancreatic head. Our patient with pT4pN0 stage 2 malignancy was safely discharged 11 days after admission a with resolution of most of her initial symptoms. Discussion: Our patient initially experienced emotional distress and was reluctant to undergo diagnostic testing. The value of a multidisciplinary team in providing comprehensive care and patient support, along with the crucial role of empathetic communication, was learned. These factors ultimately led our patient to agree to a biopsy and Whipple procedure, which significantly improved her pruritus. Further outpatient workup consists of a computed tomography scan of the chest, an outpatient PET scan, and obtaining circulating tumor DNA. Oncology recommended testing for microsatellite instability/ mismatch repair deficiency to be assessed on the tumor; if testing is positive, adjuvant chemotherapy with either FOLFOX or CAPOX was discussed. Since being discharged, our patient has followed up with surgery and is due to follow up with oncology.

The American Journal of GastroenterologyVol. 120(10S2)
Good health and well-being
Openalex Percentile: Top 32%
Pancreatic and Hepatic Oncology Research
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