Abstract
Loeys-Dietz syndrome is a rare connective tissue disorder characterized by the formation of aggressive arterial aneurysms. There are a few reports of Loeys-Dietz syndrome with pseudoaneurysms causing simultaneous pancreatic and biliary stenoses. Herein, we report the case of a 42-year-old man with Loeys-Dietz syndrome who presented with acute pancreatitis and liver dysfunction caused by a giant pancreaticoduodenal artery pseudoaneurysm compressing the main pancreatic and bile ducts. To minimize the risk of pseudoaneurysm rupture during endoscopic intervention, transcatheter arterial embolization was performed, followed by endoscopic intervention. Although initial clinical improvement was observed after endoscopic stent placement, a fistula between the pancreatic duct and the thrombosed pseudoaneurysm was detected at 4months but spontaneously closed with continued stenting. Despite persistent ductal stenosis requiring long-term stent management, the fistula had closed 1year after the initial stent placement. To the best of our knowledge, this is the first report describing a structured treatment strategy for pancreaticobiliary obstruction caused by a Loeys-Dietz syndrome-related pseudoaneurysm. This case highlights the importance of a stepwise interventional radiology-first approach and careful follow-up for the management of complex vascular compressive syndromes.
Highlights
Loeys–Dietz syndrome (LDS) is a rare, systemic hereditary connective tissue disorder caused by mutations in transforming growth factor beta receptor 1 (TGFBR1) or TGFBR2
Detection and treatment of ruptured aortic aneurysms and arterial dissections are crucial for prolonging the prognosis
Aneurysms frequently occur in major arteries, pseudoaneurysms of the pancreaticoduodenal artery leading to pancreatic or bile duct obstruction are extremely rare
Summary
Loeys–Dietz syndrome (LDS) is a rare, systemic hereditary connective tissue disorder caused by mutations in transforming growth factor beta receptor 1 (TGFBR1) or TGFBR2. We present a case report of a patient with LDS with a giant pancreaticoduodenal artery pseudoaneurysm leading to simultaneous obstructive pancreatic and biliary duct stenosis This case was successfully managed via a stepwise approach using transcatheter arterial embolization (TAE) followed by endoscopic biliary and pancreatic drainage. Endoscopic retrograde pancreatography (ERP) revealed compression and stenosis of the MPD at the pancreatic head, with upstream dilation of the distal pancreatic duct (Fig. 3d). Endoscopic retrospective cholangiography (ERC) showed compression, stenosis, and angulation of the CBD To decompress both the bile and pancreatic duct, a 5Fr × 5 cm pancreatic stent (Geenen, Cook Medical, Bloomington, IN, USA) was inserted into the MPD, while a 7Fr × 14 cm biliary stent (K-Hilar, Gadelius Medical, Tokyo, Japan) was placed in the CBD (Fig. 3e). D Endoscopic retrograde pancreatography revealed compression and stenosis of the main pancreatic duct at the pancreatic head, with upstream dilation of the distal pancreatic duct. e Both a biliary stent and a pancreatic stent were inserted
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