S3638 Metastatic Cholangiocarcinoma Presenting as an Esophageal Polyp: A Case Report

Introduction: Cholangiocarcinoma is a rare malignancy of the biliary tree and the second most common primary liver tumor. It spreads via the lymphatic system to the liver, lung, bone, and brain. Here we report a rare case of cholangiocarcinoma with metastasis to the esophagus. Case Description/Methods: A 52-year-old man presented with unintentional weight loss, nausea and vomiting. Esophagogastroduodenoscopy (EGD) and endoscopic ultrasound (EUS) revealed a distal esophageal tumor extending 3 cm into the proximal stomach. Biopsies revealed adenocarcinoma and PET-computed tomography was negative for metastases. He underwent an Ivor-Lewis esophagectomy 4 months later. The patient re-presented 32 months after surgical resection with right upper quadrant abdominal pain, vomiting and elevated liver enzymes (total bilirubin 17.7 mg/dL, direct bilirubin >10 mg/dL, alkaline phosphatase 627 U/L). Magnetic resonance cholangiopancreatography (MRCP) noted intrahepatic bile duct dilation without obstructive lesions. Repeat EGD showed an esophageal polyp at 35 cm that was resected en bloc. Pathology was consistent with submucosal gland/duct adenoma. Endoscopic retrograde cholangiopancreatography (ERCP) failed to traverse the biliary stricture, therefore 2 percutaneous transhepatic external biliary drainage catheters (PTC) were placed into the right and left hepatic systems with liver function test improvement. Follow up ERCP with direct cholangioscopy through the PTC sheath revealed a malignant stricture extending from the common hepatic to the right intrahepatic duct. This was treated with plastic stent placement and stricture biopsies confirmed invasive adenocarcinoma. The patient was subsequently found to have hepatic metastasis and was initiated on chemotherapy (gemcitabine, cisplatin and durvalumab). The initially acquired esophageal polyp resection sample was then re-evaluated and favored to be metastasis of a bile duct primary. Discussion: Metastasis of cholangiocarcinoma to the esophagus is exceedingly rare, with only 2 prior reports. This case had a unique presentation with an original unrelated primary esophageal cancer, followed by metastatic cholangiocarcinoma with esophageal involvement almost 3 years post-esophagectomy. This highlights the importance of considering metastatic disease in patients with atypical gastrointestinal symptoms and emphasizes the role of a multidisciplinary approach in managing complex cholangiocarcinoma cases.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001142012.08990.cf
Primary Topic
Metastasis and carcinoma case studies
Type
article
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article

S3638 Metastatic Cholangiocarcinoma Presenting as an Esophageal Polyp: A Case Report

Robert Pompa, Omar Shamaa, M. Ghanem, Jonathan A. Montrose
The American Journal of Gastroenterology
Metastasis and carcinoma case studies
article

S3638 Metastatic Cholangiocarcinoma Presenting as an Esophageal Polyp: A Case Report

Robert Pompa, Omar Shamaa, M. Ghanem, Jonathan A. Montrose
article en

Abstract

Introduction: Cholangiocarcinoma is a rare malignancy of the biliary tree and the second most common primary liver tumor. It spreads via the lymphatic system to the liver, lung, bone, and brain. Here we report a rare case of cholangiocarcinoma with metastasis to the esophagus. Case Description/Methods: A 52-year-old man presented with unintentional weight loss, nausea and vomiting. Esophagogastroduodenoscopy (EGD) and endoscopic ultrasound (EUS) revealed a distal esophageal tumor extending 3 cm into the proximal stomach. Biopsies revealed adenocarcinoma and PET-computed tomography was negative for metastases. He underwent an Ivor-Lewis esophagectomy 4 months later. The patient re-presented 32 months after surgical resection with right upper quadrant abdominal pain, vomiting and elevated liver enzymes (total bilirubin 17.7 mg/dL, direct bilirubin >10 mg/dL, alkaline phosphatase 627 U/L). Magnetic resonance cholangiopancreatography (MRCP) noted intrahepatic bile duct dilation without obstructive lesions. Repeat EGD showed an esophageal polyp at 35 cm that was resected en bloc. Pathology was consistent with submucosal gland/duct adenoma. Endoscopic retrograde cholangiopancreatography (ERCP) failed to traverse the biliary stricture, therefore 2 percutaneous transhepatic external biliary drainage catheters (PTC) were placed into the right and left hepatic systems with liver function test improvement. Follow up ERCP with direct cholangioscopy through the PTC sheath revealed a malignant stricture extending from the common hepatic to the right intrahepatic duct. This was treated with plastic stent placement and stricture biopsies confirmed invasive adenocarcinoma. The patient was subsequently found to have hepatic metastasis and was initiated on chemotherapy (gemcitabine, cisplatin and durvalumab). The initially acquired esophageal polyp resection sample was then re-evaluated and favored to be metastasis of a bile duct primary. Discussion: Metastasis of cholangiocarcinoma to the esophagus is exceedingly rare, with only 2 prior reports. This case had a unique presentation with an original unrelated primary esophageal cancer, followed by metastatic cholangiocarcinoma with esophageal involvement almost 3 years post-esophagectomy. This highlights the importance of considering metastatic disease in patients with atypical gastrointestinal symptoms and emphasizes the role of a multidisciplinary approach in managing complex cholangiocarcinoma cases.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 56%
Metastasis and carcinoma case studies
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