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Intrapancreatic accessory spleen: an enigmatic entity.
Namita Chavan1, Gunjan Shailesh Desai1, Chandralekha Tampi2
1Department of Gastrointestinal Surgery, Lilavati Hospital and Research Centre, Mumbai, India.
A rare case of intrapancreatic accessory spleen (IPAS) was misdiagnosed as a pancreatic neuroendocrine neoplasm (NEN) due to its hypervascular appearance. This highlights the diagnostic challenge IPAS presents, often mimicking more common pancreatic tumors.
Area of Science:
- Gastroenterology
- Surgical Pathology
- Diagnostic Imaging
Background:
- Solitary hypervascular pancreatic lesions pose diagnostic challenges.
- Common differentials include neuroendocrine neoplasms (NENs) and renal cell carcinoma metastases.
- Intrapancreatic accessory spleen (IPAS) is a rare but important differential diagnosis.
Observation:
- A 56-year-old male presented with non-specific abdominal symptoms and a pancreatic body/tail mass.
- Preoperative diagnosis suggested NEN based on elevated chromogranin and CT findings.
- The patient underwent spleen-preserving distal pancreatectomy.
Findings:
- Histopathology revealed the pancreatic lesion to be an IPAS.
- This contrasts with the preoperative diagnosis of NEN.
- IPAS can mimic other pancreatic space-occupying lesions.
Implications:
- This case underscores the importance of considering rare differentials like IPAS.
- Accurate preoperative diagnosis of pancreatic lesions is crucial for appropriate management.
- Understanding IPAS as a mimic aids in surgical planning and patient outcomes.
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