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Intrapancreatic accessory spleen: a diagnostic dilemma
Bing-Qi Li1, Xie-Qun Xu1, Jun-Chao Guo1
1Department of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences/Peking Union Medical College, Beijing, China.
Intrapancreatic accessory spleen (IPAS) is a rare finding. This review summarizes IPAS epidemiology, diagnosis, and treatment, highlighting its potential confusion with pancreatic neuroendocrine tumors.
Area of Science:
- Gastroenterology
- Surgical Pathology
- Radiology
Background:
- Intrapancreatic accessory spleen (IPAS) is an uncommon clinical finding.
- Accurate diagnosis and treatment strategies for IPAS are not well-established.
Purpose of the Study:
- To review and summarize the epidemiology, diagnosis, and treatment of IPAS.
- To improve clinical recognition and management of IPAS.
Main Methods:
- Systematic literature search of MEDLINE and EMBASE databases for IPAS cases.
- Analysis of epidemiological features, diagnostic methods, and treatment outcomes.
Main Results:
- 105 patients with IPAS were identified; 73% were incidental findings.
- IPAS size was larger in patients with prior splenectomy (2.5 cm vs 1.5 cm).
- Definitive preoperative diagnosis was challenging; 55% underwent surgery, often misdiagnosed as pancreatic neuroendocrine tumors (p-NET).
Conclusions:
- IPAS should be considered in the differential diagnosis of incidental pancreatic lesions, particularly in patients with a history of splenectomy.
- Accurate preoperative diagnosis is crucial to avoid unnecessary surgery.
- Multimodal diagnostic approaches may be necessary for definitive IPAS identification.
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