Solid Serous Cystadenoma Mimicking Neuroendocrine Tumor of the Pancreas: A Case Report

Solid-type serous cystadenoma (SSCA) of the pancreas is an extremely rare benign condition among pancreatic cystic neoplasms. Although the imaging characteristics are not pathognomonic, this entity may mimic other solid pancreatic tumors. In particular, it can closely resemble a pancreatic neuroendocrine neoplasm (pNEN) on radiologic studies. We report the case of a 67-year-old woman who presented with abdominal pain. Preoperative abdominal magnetic resonance imaging (MRI) with contrast demonstrated a solid, hypervascular lesion at the pancreas, measuring 3.5 × 2.2 × 1.9 cm, with marked enhancement on dynamic imaging. A nonfunctioning pancreatic neuroendocrine tumor was initially suspected. The patient underwent laparoscopic pancreaticoduodenectomy. Histopathologic examination revealed a solid variant of serous cystadenoma, a rare subtype of pancreatic cysts. The patient remains asymptomatic, with no evidence of recurrence or residual disease at 7 years postoperatively. This case highlights the diagnostic challenge of distinguishing solid-type serous cystadenomas from other pancreatic lesions based on imaging alone, underscoring the role of pathology in definitive diagnosis.

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Journal
Case Reports in Gastrointestinal Medicine
Published
2025-01-01
DOI
https://doi.org/10.1155/crgm/4945872
Primary Topic
Pancreatic and Hepatic Oncology Research
Type
article
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article

Solid Serous Cystadenoma Mimicking Neuroendocrine Tumor of the Pancreas: A Case Report

Adriano Carneiro da Costa, Kumar Jayant, Isabella Reccia, Flávio Silano et al.
Case Reports in Gastrointestinal Medicine
Pancreatic and Hepatic Oncology Research
article

Solid Serous Cystadenoma Mimicking Neuroendocrine Tumor of the Pancreas: A Case Report

Adriano Carneiro da Costa, Kumar Jayant, Isabella Reccia, Flávio Silano, Paulo Cezar G AMARAL, Nagy Habib, Camila Ramos Martins, Mohamed Ali Chaouch
article en

Abstract

Solid-type serous cystadenoma (SSCA) of the pancreas is an extremely rare benign condition among pancreatic cystic neoplasms. Although the imaging characteristics are not pathognomonic, this entity may mimic other solid pancreatic tumors. In particular, it can closely resemble a pancreatic neuroendocrine neoplasm (pNEN) on radiologic studies. We report the case of a 67-year-old woman who presented with abdominal pain. Preoperative abdominal magnetic resonance imaging (MRI) with contrast demonstrated a solid, hypervascular lesion at the pancreas, measuring 3.5 × 2.2 × 1.9 cm, with marked enhancement on dynamic imaging. A nonfunctioning pancreatic neuroendocrine tumor was initially suspected. The patient underwent laparoscopic pancreaticoduodenectomy. Histopathologic examination revealed a solid variant of serous cystadenoma, a rare subtype of pancreatic cysts. The patient remains asymptomatic, with no evidence of recurrence or residual disease at 7 years postoperatively. This case highlights the diagnostic challenge of distinguishing solid-type serous cystadenomas from other pancreatic lesions based on imaging alone, underscoring the role of pathology in definitive diagnosis.

Case Reports in Gastrointestinal MedicineVol. 2025(1)
University of Monastir (TN), Universidade Federal de Pernambuco (BR), Hammersmith Hospital (GB), Hospital São Rafael (BR), Hospital das Clínicas da Universidade Federal de Pernambuco (BR), Imperial College London (GB)
Openalex Percentile: Top 68%
Pancreatic and Hepatic Oncology Research
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