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DOI: 10.1055/s-0033-1359158
Pancreatic metastasis of a meningeal hemangiopericytoma: a rare cause of obstructive jaundice
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Publication History
Publication Date:
22 April 2014 (online)
A 52-year-old man presented to the emergency department with jaundice, pale stools, and dark urine for 1 week, having lost 15 % of his body weight during the previous month. He was a heavy smoker and drinker. He had been diagnosed 4 months previously with a meningeal hemangiopericytoma that had been surgically resected then treated with cranial external radiotherapy. Laboratory evaluation was remarkable for hyperbilirubinemia (9 mg/dL) and cholestasis (alkaline phosphatase [ALP] 1300 IU/L). Magnetic resonance imaging (MRI) revealed a 25-mm pancreatic head mass and upstream dilatation of the bile ducts but a normal main pancreatic duct ([Fig. 1]). A second 15-mm mass in the uncinate process was also noted.


The patient underwent an endoscopic ultrasound (EUS) using a linear echoendoscope (UCT 10 – 140 AL5; Olympus), which revealed a slightly heterogeneous, hypoechoic, ill-defined mass in the pancreatic head from which a fine needle aspiration (FNA) was taken with a 25G needle (Wilson Cook; [Fig. 2 a]). The second smaller lesion was also visualized in the uncinate process close to the superior mesenteric vein ([Fig. 2 b]).
Fig. 2 Endoscopic ultrasound (EUS) images showing: a a 21-mm hypoechoic heterogeneous pancreatic head mass which is being sampled by fine needle aspiration (FNA) using a 25G needle; b a smaller 14-mm hypoechoic mass in the uncinate process close to the superior mesenteric vein.




During the same session, endoscopic retrograde cholangiopancreatography (ERCP) was performed as a tandem procedure and a 7-cm long, 7-Fr plastic biliary prosthesis was placed to allow adequate biliary drainage. Evaluation of the cell block cytology was consistent with hemangiopericytoma ([Fig. 3]). The patient died 2 weeks later from uncontrolled seizures.


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Competing interests: None
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