JGH Open (Feb 2021)

A case of juvenile eosinophilic cholangitis: Rapid peripheral blood hypereosinophilia after admission leading to diagnosis

  • Shusaku Fukatsu,
  • Katsuya Kitamura,
  • Yasutsugu Asai,
  • Kazumasa Nagai,
  • Miho Kikuchi,
  • Kyoko Asano,
  • Kenichi Tadokoro,
  • Fumito Yamanishi,
  • Yusuke Tomita,
  • Masakazu Abe,
  • Takuya Wada,
  • Yubu Matsue,
  • Daisuke Nutahara,
  • Junichi Taira,
  • Hironori Nakamura,
  • Takao Itoi

DOI
https://doi.org/10.1002/jgh3.12454
Journal volume & issue
Vol. 5, no. 2
pp. 314 – 316

Abstract

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Abstract A 15‐year‐old boy was referred to our hospital with elevated hepatobiliary enzyme levels and jaundice. Magnetic resonance cholangiopancreatography performed at the previous medical facility revealed a stricture of the intrahepatic and extrahepatic bile duct. Computed tomography showed dilatation and wall thickness of the intrahepatic bile ducts. Primary sclerosing cholangitis or cholangiocarcinoma was suspected. Endoscopic retrograde cholangiopancreatography (ERCP) showed stricture in the intrahepatic and extrahepatic bile duct. On admission, the eosinophil count in the peripheral blood was normal; however, rapid hypereosinophilia in the peripheral blood was observed after admission, leading us to suspect eosinophilic cholangitis (EC). A bile duct biopsy showed inflammatory cells and eosinophil infiltration during a second ERCP. The patient was diagnosed with EC based on histopathology.

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