Surgical case reports · 2026
Pancreaticobiliary Fistula Caused by Intraductal Papillary Mucinous Adenoma Requiring Pancreaticoduodenectomy.
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Nagao Mina, Suto Hironobu, Matsukawa Hiroyuki, Fujiwara Junichi, Kagawa Seiko, Fuke Takuro, Shimizu Yoshio, Nishigaki Arata, Ando Yasuhisa, Oshima Minoru, Okano Keiichi
Аннотация
INTRODUCTION: Fistula formation from the intraductal papillary mucinous neoplasm (IPMN) into neighboring organs is rare. We describe a case of pancreaticobiliary fistula with obstructive jaundice caused by an intraductal papillary mucinous adenoma (IPMA).
CASE PRESENTATION: An 81-year-old man who was incidentally diagnosed with IPMN 11 years previously based on follow-up CT performed after nephrectomy for renal cell carcinoma. Gradual dilation of the main pancreatic duct was observed over time, confirming the high-risk stigmata for which surgery was recommended; however, the patient declined and was managed under surveillance. At a routine diabetes clinic visit, blood tests revealed inflammatory markers and hepatobiliary enzymes. Contrast-enhanced CT revealed a pancreatic head IPMN in extensive contact with the common bile duct with partial communication. Endoscopic nasobiliary drainage (ENBD) was performed, but resolution of jaundice proved difficult due to obstruction by mucin; therefore, we performed a subtotal stomach-preserving pancreaticoduodenectomy (SSPPD). Severe inflammation was observed around the pancreas and bile ducts at the surgical site. The postoperative course was favorable, and the patient was discharged on the POD 16. The histopathological diagnosis was intestinal-type IPMA.
CONCLUSIONS: Most reported IPMN-related organ fistulas result from direct invasion by IPMC. By contrast, IPMA-related fistulation is exceedingly rare. We present an intestinal-type IPMA complicated by pancreaticobiliary fistula in which mucin defeated ENBD, necessitating SSPPD, and the patient had an uneventful recovery. This case shows that fistulation can occur even without IPMC and that early surgery should be considered in IPMN patients with pancreatobiliary fistula.
CASE PRESENTATION: An 81-year-old man who was incidentally diagnosed with IPMN 11 years previously based on follow-up CT performed after nephrectomy for renal cell carcinoma. Gradual dilation of the main pancreatic duct was observed over time, confirming the high-risk stigmata for which surgery was recommended; however, the patient declined and was managed under surveillance. At a routine diabetes clinic visit, blood tests revealed inflammatory markers and hepatobiliary enzymes. Contrast-enhanced CT revealed a pancreatic head IPMN in extensive contact with the common bile duct with partial communication. Endoscopic nasobiliary drainage (ENBD) was performed, but resolution of jaundice proved difficult due to obstruction by mucin; therefore, we performed a subtotal stomach-preserving pancreaticoduodenectomy (SSPPD). Severe inflammation was observed around the pancreas and bile ducts at the surgical site. The postoperative course was favorable, and the patient was discharged on the POD 16. The histopathological diagnosis was intestinal-type IPMA.
CONCLUSIONS: Most reported IPMN-related organ fistulas result from direct invasion by IPMC. By contrast, IPMA-related fistulation is exceedingly rare. We present an intestinal-type IPMA complicated by pancreaticobiliary fistula in which mucin defeated ENBD, necessitating SSPPD, and the patient had an uneventful recovery. This case shows that fistulation can occur even without IPMC and that early surgery should be considered in IPMN patients with pancreatobiliary fistula.