S6231 From Syncope to Diagnosis: The Unexpected Duodenal Neuroendocrine Tumor in an Elderly

Introduction: Neuroendocrine tumors (NETs) have been increasing in incidence due to higher rates of endoscopic evaluation. They constitute 2% of all gastrointestinal malignancies. They are more prevalent in females. NETS most commonly develop in the small intestine. They are mostly non-functional, although a considerable proportion secrete gastric acid and in turn, can cause duodenal ulceration. Carcinoid syndrome is rare in duodenal NETs and mostly occurs in the setting of hepatic metastases. Case Description/Methods: A 78-year-old man with a history of hypertension, hyperlipidemia, diabetes mellitus, paroxysmal atrial fibrillation on apixaban, and left lower extremity weakness due to childhood polio presented to the emergency department following an episode of syncope. He reported intermittent melena for the past 2-3 months but denied hematemesis or hematochezia. Initial labs showed stable hemoglobin (14.3 g/dL) and platelets (249,000/μL), but he had hypokalemia (2.8 mmol/L) and atrial fibrillation with rapid ventricular response on EKG. Given his melena and anticoagulation use, gastroenterology was consulted for further evaluation. During upper endoscopy, a 6 cm x 6 cm polyp was found in the duodenal bulb. Its appearance was benign, but due to the size and location being atypical, a biopsy was obtained. Biopsy confirmed a well-differentiated duodenal neuroendocrine tumor (DNET), with staining positive for synaptophysin, chromogranin, CD56 and focally AE 1/3. Imaging showed no distant metastases. Initially, the patient's syncope was attributed to arrhythmia secondary to hypokalemia rather than DNET. Given his age and comorbidities, he was managed conservatively along with close surveillance and was given follow-up with an advanced endoscopist and hematology/oncology. Discussion: This case highlights an unusual presentation of NET in an elderly patient with multiple comorbidities, emphasizing the importance of endoscopic evaluation in unexplained gastrointestinal bleeding, even in the absence of anemia. Occupational risk factors, including smoking and coal mine exposure, may have contributed to his malignancy. Further studies are needed to explore NETs in elderly populations.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001153384.62747.13
Primary Topic
Neuroendocrine Tumor Research Advances
Type
article
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article

S6231 From Syncope to Diagnosis: The Unexpected Duodenal Neuroendocrine Tumor in an Elderly

The American Journal of Gastroenterology
Neuroendocrine Tumor Research Advances
article

S6231 From Syncope to Diagnosis: The Unexpected Duodenal Neuroendocrine Tumor in an Elderly

article en

Abstract

Introduction: Neuroendocrine tumors (NETs) have been increasing in incidence due to higher rates of endoscopic evaluation. They constitute 2% of all gastrointestinal malignancies. They are more prevalent in females. NETS most commonly develop in the small intestine. They are mostly non-functional, although a considerable proportion secrete gastric acid and in turn, can cause duodenal ulceration. Carcinoid syndrome is rare in duodenal NETs and mostly occurs in the setting of hepatic metastases. Case Description/Methods: A 78-year-old man with a history of hypertension, hyperlipidemia, diabetes mellitus, paroxysmal atrial fibrillation on apixaban, and left lower extremity weakness due to childhood polio presented to the emergency department following an episode of syncope. He reported intermittent melena for the past 2-3 months but denied hematemesis or hematochezia. Initial labs showed stable hemoglobin (14.3 g/dL) and platelets (249,000/μL), but he had hypokalemia (2.8 mmol/L) and atrial fibrillation with rapid ventricular response on EKG. Given his melena and anticoagulation use, gastroenterology was consulted for further evaluation. During upper endoscopy, a 6 cm x 6 cm polyp was found in the duodenal bulb. Its appearance was benign, but due to the size and location being atypical, a biopsy was obtained. Biopsy confirmed a well-differentiated duodenal neuroendocrine tumor (DNET), with staining positive for synaptophysin, chromogranin, CD56 and focally AE 1/3. Imaging showed no distant metastases. Initially, the patient's syncope was attributed to arrhythmia secondary to hypokalemia rather than DNET. Given his age and comorbidities, he was managed conservatively along with close surveillance and was given follow-up with an advanced endoscopist and hematology/oncology. Discussion: This case highlights an unusual presentation of NET in an elderly patient with multiple comorbidities, emphasizing the importance of endoscopic evaluation in unexplained gastrointestinal bleeding, even in the absence of anemia. Occupational risk factors, including smoking and coal mine exposure, may have contributed to his malignancy. Further studies are needed to explore NETs in elderly populations.

The American Journal of GastroenterologyVol. 120(10S2)
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Neuroendocrine Tumor Research Advances
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