INTRODUCTION
Pancreatic cancer is among the most aggressive gastrointestinal malignancies, often diagnosed at an advanced stage. It has a high mortality rate due to late diagnosis [
1]. Common metastatic sites include lymph nodes, liver, lungs, and peritoneum, with gastric involvement being exceedingly rare [
2]. Differentiating between primary gastric lesions and secondary invasion by pancreatic cancer is clinically challenging, especially when endoscopic appearances mimic benign pathology [
3]. Herein, we report a case in which pancreatic cancer initially presented with endoscopic features suggestive of a benign gastric adenoma.
CASE REPORT
A 76-year-old male underwent screening esophagogastroduodenoscopy, revealing a 1 cm ulcerative lesion (
Fig. 1) on the lesser curvature of the stomach. The initial endoscopic report described the lesion merely as a gastric ulcer and two biopsy specimens were obtained which indicated tubulovillous adenoma with low-grade dysplasia.
He was referred to our department for further management. He reported mild abdominal fullness and had central obesity, but no abdominal tenderness or signs of peritoneal irritation were noted on physical examination.
Although the initial endoscopic report described the lesion simply as a gastric ulcer, its irregular margins and granular surface raised the possibility of early gastric cancer, and endoscopic submucosal dissection (ESD) was initially planned. Routine laboratory tests revealed no anemia (hemoglobin 14.2 g/dL), no hypoalbuminemia (albumin 3.7 g/dL), and normal liver and renal function. Tumor marker showed elevated carcinoembryonic antigen (CEA) at 23.0 ng/mL (normal <2.5 ng/mL), while alpha-fetoprotein and carbohydrate antigen 19-9 (CA 19-9) were within normal limits. Colonoscopy was performed to rule out colorectal neoplasia and confirmed only benign tubular adenomas.
A second-look endoscopy revealed an irregular, non-healing ulcer without a clean base. Notably, muscle fibers consistent with the muscularis propria layer were directly exposed at the ulcer base, raising strong concern for deep infiltration. Additional findings such as mucosal friability and spontaneous oozing further heightened suspicion of malignancy (
Fig. 2), leading to cancellation of ESD.
Re-biopsy showed atypical findings such as irregular, infiltrative glands embedded in a desmoplastic stroma, cribriform architecture, nuclear pleomorphism, hyperchromasia, and loss of polarity—suggestive of malignancy (
Fig. 3), prompting further evaluation. An abdominal CT was performed, revealing an ill-defined mass in the pancreatic body and tail (
Fig. 4) with main pancreatic duct dilatation and direct invasion into the gastric wall. Additionally, massive ascites and peritoneal carcinomatosis were noted. Positron emission tomography-CT (PET-CT) confirmed hypermetabolic activity in the pancreatic lesion (
Fig. 5) [
4].
Ascitic fluid analysis demonstrated markedly elevated CEA levels, supporting peritoneal carcinomatosis [
5]. The final diagnosis confirmed advanced pancreatic adenocarcinoma with direct gastric invasion. The patient declined chemotherapy and was referred to hospice care.
DISCUSSION
Although primary gastric lesions are more common, extrinsic malignancy should be considered when endoscopic findings and pathology are not concordant. In this case, the initial tissue sampling suggested a benign lesion, but the lesion’s morphology and progression raised suspicion. Pancreatic cancers involving the stomach tend to originate from the body or tail and spread via direct extension [
6]. Clinically, such lesions can resemble primary gastric ulcers, making evaluation complex.
Tumor markers such as CA 19-9 may not be elevated in all pancreatic cancers; the extremely low CA 19-9 in this patient illustrates that tumor markers alone may not be reliable in excluding pancreatic cancer [
7]. Radiological correlation using CT and PET-CT is therefore essential to detect extra-luminal disease [
4].
This case supports the use of repeated endoscopic evaluation and imaging when discrepancies between clinical, endoscopic, and histologic findings exist. Biopsies of ulcerative lesions may occasionally miss submucosal or externally infiltrating tumors, especially those of extrinsic origin. This highlights the limitations of superficial tissue sampling and the potential value of advanced techniques such as endoscopic ultrasound-guided fine needle aspiration. 8,9
In conclusion, this case highlights the importance of considering extrinsic malignancy when encountering atypical gastric lesions that are discordant with biopsy findings. A multidisciplinary diagnostic approach that integrates endoscopic morphology, histopathological findings, and cross-sectional imaging is essential to prevent misdiagnosis and ensure timely management.