Journal of the Pancreas Open Access

Keywords

Endosonography; Neuroendocrine Tumors; Pancreatitis

INTRODUCTION

Recurrent acute pancreatitis can rarely be due to an obstructive pathology at the ampulla of Vater. EUS is an excellent modality for detecting small ampullary pathology. Recently wirsungocele has been described as an etiological factor for recurrent pancreatitis. We encountered a patient who had recurrent pancreatitis due to a wirsungocele and a small neuroendocrine tumor at the ampulla of Vater, both diagnosed by endosonography.

CASE REPORT

A 63-year-old male had two episodes of acute pancreatitis by biochemistry and abdominal ultrasonography. EUS findings showed an ampullary mass and cystic dilatation of terminal portion of duct of Wirsung suggestive of wirsungocele (Figures 1 and 2). EUS guided FNA from the ampulla suggested a neuroendocrine tumor. MRCP confirmed EUS findings of wirsungocele and ampullary mass (Figure 3). ERCP (Figure 4) and endoscopic ampullectomy was then performed and patient made an uneventful recovery. The histopathological examination and immunohistochemistry showed neuroendocrine tumor (pathological classification: G1) with cells expressing synaptophysin and chromogranin (Figure 5). The Mib proliferation index was less than 2%. The pancreatic duct was seen well dilated within the tumor tissue.

DISCUSSION

Wirsungocele is the term coined for cystic dilation of the terminal part of the duct of Wirsung. We found a total of eight cases of wirsungocele described in five papers indexed in PubMed [1, 2, 3, 4, 5]. Abu-Hamda et al. first described wirsungocele as an incidental finding on ERCP [1]. Four of these cases (50.0%) of wirsungoceles are associated with acute recurrent pancreatitis [1, 2, 3, 4, 5]. Five reported cases (62.5%) are males and age of presentation is after 4th decade [1, 2, 3, 4, 5]. Endoscopic pancreatic sphincterotomy and stenting appears very effective and durable [2, 3, 4].

Our patient also had good symptom relief following endotherapy. EUS as a diagnostic tool has not been used adequately so far. For the first time we could demonstrate wirsungocele on EUS and its association with neuroendocrine tumor.

Ampullary neuroendocrine tumor is a rare entity, and constitutes less than 1% of all gastrointestinal neuroendocrine tumors [5]. In our case possibility of wirsungocele formation due to long standing obstruction by the neuroendocrine tumor is unlikely. A complete upstream ductal dilatation is more likely to occur due to a tumor. The episodes of acute recurrent pancreatitis were more likely to be due to wirsungocele as the duct is not compressed by the tumor on histology.

CONCLUSION

This case report highlights the diagnostic utility of EUS in diagnosing small ampullary pathology like wirsungocele and neuroendocrine tumor. The association of wirsungocele with neuroendocrine tumor of ampulla and recurrent pancreatitis has also been reported for the first time.

Conflict interests

The authors have no potential conflict of interest

References

1. Abu-Hamda EM, Baron TH. Cystic dilatation of the intraduodenal portion of the duct of Wirsung (Wirsungocele). Gastrointest Endosc 2004; 59:745- 7.
2. Rajesh Gupta, Sandeep Lakhtakia, Manu Tandan, Darisetty Santosh, Guduru Venkat Rao, Duvvuru Nageshwar Reddy Recurrent Acute Pancreatitis and Wirsungocele: A Case Report and Review of Literature. JOP 2008; 9:531-533.
3. Gabbrielli A, Bernardoni L, Manfredi R, Frulloni L, Benini L, Bassi C, Vantini I, Pederzoli P Wirsungocele. A Rare Cause of Severe Necrotic Acute Pancreatitis. JOP 2010 ; 11(5 Suppl):526.
4. Djalma Ernesto Coelho, José Celso Ardengh, Eder Rios de Lima-Filho, José Flávio Coelho. Different clinical aspects of Wirsungocele: case series of three patients and review of literature. Acta Gastroenterol Latinoam 2011;41:230-233.
5. Sang Won Kim, Sung Shick Jou Jong K,yu Han, Hyung Hwan Kim, Young Tong Kim. Imaging Findings of Wirsungocele: A Report of Two Cases. J Korean Radiol Soc 2008;59:317-320.