S5678 Lightning Strikes Twice: A Rare Case of Esophageal Adenocarcinoma and Neuroendocrine Tumor Co-Diagnosis

Introduction: The incidence rate of esophageal cancer and neuroendocrine tumors, as per the National Cancer Institute (NCI), are both reported to be approximately 1% of all cancer cases diagnosed. This case explores the unlikely diagnosis of an individual who was found to have both esophageal and neuroendocrine tumors as a primary malignancy during a hospitalization event. Case Description/Methods: A 51-year-old man with a past medical history of alcohol use disorder, OSA, depression, gastroesophageal reflux disease, and iron deficiency anemia presented for alcohol withdrawal. The patient endorsed right upper quadrant pain which had been intermittently occurring for the past 4 months, fatigue, and lightheadedness. On admission, the patient was sinus tachycardic with all other vitals stable. Computed tomography (CT) of the chest, abdomen, and pelvis demonstrated incidental marked circumferential thickening in the distal esophageal wall, enlarged left celiac lymph nodes concerning for metastatic adenopathy, and a suspected 4.3 × 3.4 cm right hepatic lobe lesion, concerning for metastatic disease. EGD was performed and demonstrated a partially obstructing, friable, granular, and nodular mass at the distal esophagus. Pathology was found to demonstrate poorly differentiated adenocarcinoma. Ultrasound of the right upper quadrant demonstrated numerous hepatic masses up to 5.8 cm in the right hepatic lobe. Liver biopsy was completed with pathology demonstrating well-differentiated neuroendocrine tumor. The patient was referred to oncology for PET scan completion and treatment. In addition, the patient was referred to thoracic surgery for evaluation and treatment of esophageal cancer. Discussion: Esophageal and neuroendocrine tumors are both rare processes with a low incidence in the general population. The co-existence of these 2 pathologic processes are rarely reported in literature. Although the cancers may be distinct histologically, this case entertains the possibility of ascertainment bias where neuroendocrine tumors may be more easily identified than esophageal cancer. In the case above, the esophageal wall thickening was an incidental finding when the main area of concern was the patient’s abdominal pain on presentation. Further research and reporting may be needed to provide a clearer relation between the 2 tumors.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001150172.49432.c2
Primary Topic
Neuroendocrine Tumor Research Advances
Type
article
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article

S5678 Lightning Strikes Twice: A Rare Case of Esophageal Adenocarcinoma and Neuroendocrine Tumor Co-Diagnosis

The American Journal of Gastroenterology
Neuroendocrine Tumor Research Advances
article

S5678 Lightning Strikes Twice: A Rare Case of Esophageal Adenocarcinoma and Neuroendocrine Tumor Co-Diagnosis

article en

Abstract

Introduction: The incidence rate of esophageal cancer and neuroendocrine tumors, as per the National Cancer Institute (NCI), are both reported to be approximately 1% of all cancer cases diagnosed. This case explores the unlikely diagnosis of an individual who was found to have both esophageal and neuroendocrine tumors as a primary malignancy during a hospitalization event. Case Description/Methods: A 51-year-old man with a past medical history of alcohol use disorder, OSA, depression, gastroesophageal reflux disease, and iron deficiency anemia presented for alcohol withdrawal. The patient endorsed right upper quadrant pain which had been intermittently occurring for the past 4 months, fatigue, and lightheadedness. On admission, the patient was sinus tachycardic with all other vitals stable. Computed tomography (CT) of the chest, abdomen, and pelvis demonstrated incidental marked circumferential thickening in the distal esophageal wall, enlarged left celiac lymph nodes concerning for metastatic adenopathy, and a suspected 4.3 × 3.4 cm right hepatic lobe lesion, concerning for metastatic disease. EGD was performed and demonstrated a partially obstructing, friable, granular, and nodular mass at the distal esophagus. Pathology was found to demonstrate poorly differentiated adenocarcinoma. Ultrasound of the right upper quadrant demonstrated numerous hepatic masses up to 5.8 cm in the right hepatic lobe. Liver biopsy was completed with pathology demonstrating well-differentiated neuroendocrine tumor. The patient was referred to oncology for PET scan completion and treatment. In addition, the patient was referred to thoracic surgery for evaluation and treatment of esophageal cancer. Discussion: Esophageal and neuroendocrine tumors are both rare processes with a low incidence in the general population. The co-existence of these 2 pathologic processes are rarely reported in literature. Although the cancers may be distinct histologically, this case entertains the possibility of ascertainment bias where neuroendocrine tumors may be more easily identified than esophageal cancer. In the case above, the esophageal wall thickening was an incidental finding when the main area of concern was the patient’s abdominal pain on presentation. Further research and reporting may be needed to provide a clearer relation between the 2 tumors.

The American Journal of GastroenterologyVol. 120(10S2)
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Neuroendocrine Tumor Research Advances
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S5678 Lightning Strikes Twice: A Rare Case of Esophageal Adenocarcinoma and Neuroendocrine Tumor Co-Diagnosis · The American Journal of Gastroenterology (2025) | TGRS Research Map | TGRS