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Pancreatic Adenocarcinoma With Rare Sigmoid Colon Metastasis

Kahl, Ryan DO1; George, Khalid MD1; Patel, Kruti DO2; Stawick, Laurence MD1

doi: 10.14309/crj.0000000000000132

ABSTRACT Pancreatic cancer carries a poor prognosis and given insidious symptoms has often metastasized at the time of presentation. Common sites of metastasis involve liver, lungs, regional lymph nodes, or peritoneum. Colonic metastasis is rare, with only a few previous descriptions in the literature. We report a case of a 91-year-old woman with presumed pancreatic adenocarcinoma based on pathology and imaging, with colonic metastasis presenting as colonic obstruction.

1Department of Gastroenterology, Ascension Providence-Providence Park Hospital, Southfield, MI

2Department of Gastroenterology, Ascension Genesys Hospital, Grand Blanc, MI

Correspondence: Ryan Kahl, DO, Department of Gastroenterology, Ascension Providence-Providence Park Hospital, 22250 Providence Dr, Suite 301, Southfield, MI 48075 (

Received December 10, 2018

Accepted May 10, 2019

Online date: July 10, 2019

This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.

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Pancreatic adenocarcinoma has an extremely poor prognosis. The insidious symptoms are often unnoticed at onset until late stage or metastatic changes induce more alarming symptoms. When diagnosed, pancreatic adenocarcinoma has often metastasized, most often to liver, lungs, regional lymph nodes, or peritoneum.1–3 Colonic metastasis is extremely rare, with a few previous descriptions in the literature.1,3–5 We report a case of pancreatic adenocarcinoma with colonic metastasis presenting as colonic obstruction.

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A 91-year-old woman with a history of hypertension, gastroesophageal reflux disease, and recently diagnosed diabetes mellitus presented with nausea, early satiety, and unintentional 13.6 kg weight loss. She reported a long-standing history of constipation without hematochezia, melena, or change in stool caliber. Initial abdominal radiograph did not reveal distention. Abdominal examination was remarkable for positive bowel sounds and abdominal pain without distention, palpable masses, or jaundice. Laboratory values were not consistent with hepatobiliary obstruction, with alkaline phosphatase of 24 U/L, aspartate aminotransferase of 24 U/L, alanine transaminase of 11 U/L, and total bilirubin of 0.3 mg/dL.

The patient initially received barium swallow to rule out esophageal stricture, and subsequent esophagogastroduodenoscopy revealed gastritis without signs of gastric outlet obstruction due to ulcer or mass. Shortly after, she reported worsening abdominal pain and distention. Repeat abdominal radiograph showed 14-cm dilated right colon (cecum through transverse colon) with retained barium contrast. Computerized tomography (CT) scan was not performed due to concern for artifact and nondiagnostic imaging in setting of previous barium contrast administration.

Flexible sigmoidoscopy was performed after enema preparation, and decompression was attempted; however, severe stenosis of unknown length was found in the sigmoid colon and was unable to be traversed. Patient then underwent a palliative sigmoid colectomy with end colostomy. Follow-up CT with contrast revealed an ill-defined pancreatic head mass measuring 4 × 3.3 cm, encasing celiac artery and proximal branches (Figure 1). Tumor markers were significant for carbohydrate antigen 19-9 of 7,480 U/mL, carcinoembryonic antigen 3.6 ng/mL, and cancer antigen 125 190 U/mL. Pathology confirmed well-differentiated adenocarcinoma of likely metastatic origin. Immunostaining profile showed cytokeratin 7 positive, cytokeratin 20 negative, and caudal-type homeobox transcription factor 2 negative (Figure 2). Given cytokeratin 7 positive and cytokeratin 20 negative, the primary site of adenocarcinoma was presumed to be pancreatic in origin, especially given CT imaging findings.6 The patient desired comfort-focused care and was discharged home with hospice.

Figure 1

Figure 1

Figure 2

Figure 2

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Pancreatic cancer continues to carry a very poor prognosis and is the fourth leading cause of cancer deaths in the United States.7,8 The long-term relative survival rate of pancreatic cancer has not substantially changed over the past few decades, and analysis of the most recent decade shows relative survival rate of 28.2% in the first year and 6.9% at 5 years.9 The retroperitoneal location of the pancreas allows for metastatic dissemination to many organs, the most common of which are liver, lungs, regional lymph nodes, and peritoneum.1–3

Colonic metastasis of pancreatic cancer is extremely rare, with a few previously described cases in the literature.1,3–5 Three of the previous cases followed pancreatic lesion resection, and diagnosis was made after pathologic examination.3–5 One previous case, like ours, had an initial presentation with weight loss and imaging suspicious for primary colon malignancy, with the later identification showing pancreatic cancer metastasis.1 Our case is the first case, to our knowledge, of pancreatic adenocarcinoma presenting with sigmoid colon metastasis.

The presentation of pancreatic cancer is often insidious, with nonspecific symptoms such as nausea and anorexia, which delay diagnosis until other more ominous symptoms such as weight loss, abdominal pain, or gastrointestinal symptoms develop.2 Risk factors for pancreatic cancer include tobacco smoking, diabetes mellitus, family history of pancreatitis, metabolic syndrome, and Helicobacter pylori infection.10 Our patient had second-hand tobacco exposure and recently diagnosed with diabetes mellitus. Multiple studies have demonstrated a strong association between pancreatic ductal adenocarcinoma and diabetes mellitus, with the strongest associations within the first few years after diagnosis.11 A 2014 meta-analysis showed a pooled relative risk of 2.08 (95% confidence interval: 1.87–2.32) for pancreatic ductal adenocarcinoma with diabetes than with those without.11 The association between diabetes and pancreatic adenocarcinoma is thought to be mediated by tumor-secreted products and less associated with tumor size or stage.11,12 Current studies attempting to identify serologic markers with increased risk are underway; however, at present, imaging for screening purposes cannot be recommended.12 Her presentation with unintentional 13.6 kg weight loss, early satiety, and colonic obstruction is not a typical presentation of pancreatic adenocarcinoma. Although very rare, the differential for patients presenting with colonic obstruction and concern for colonic mass with a recent diagnosis of diabetes mellitus should include pancreatic adenocarcinoma.

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Author contributions: All authors wrote the manuscript. K. George edited the manuscript. K. Patel performed the literature review. R. Kahl is the article guarantor.

Financial disclosures: None to report.

Informed consent was obtained for this case report.

Previous presentation: This case was presented at the World Congress of Gastroenterology at ACG 2017; October 13–18, 2017; Orlando, Florida.

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