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Volume 13 Issue 6
Nov.  2022
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ZOU Long, WANG Qiang, WU Xi, WANG Zhiwei, YANG Aiming. Eosinophilic Enteritis Accompanied with Recurrent Acute Pancreatitis: A Case Resport[J]. Medical Journal of Peking Union Medical College Hospital, 2022, 13(6): 1100-1104. DOI: 10.12290/xhyxzz.2021-0803
Citation: ZOU Long, WANG Qiang, WU Xi, WANG Zhiwei, YANG Aiming. Eosinophilic Enteritis Accompanied with Recurrent Acute Pancreatitis: A Case Resport[J]. Medical Journal of Peking Union Medical College Hospital, 2022, 13(6): 1100-1104. DOI: 10.12290/xhyxzz.2021-0803
shu

Eosinophilic Enteritis Accompanied with Recurrent Acute Pancreatitis: A Case Resport

  • 1.

    Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China

  • 2.

    Department of Gastroenterology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China

  • 3.

    Department of Radiology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China

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Beijing's Key Construction of First-class Professional Projects 2021zlgc1106

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  • Corresponding author:

    WANG Qiang, E-mail: pekingunion@aliyun.com

  • Received Date: December 26, 2021
  • Accepted Date: January 23, 2022
  • Available Online: March 04, 2022
  • Issue Publish Date: November 29, 2022
    Graphical Abstract
    • Abstract
  • This was a patient with a medical history of aspirin-aggravated respiratory disease present with eosinophilic enteritis and recurrent acute pancreatitis. Eosinophilic granulomatosis with polyangiitis was clinically suspected due to the clinical presentation of multiple systems and the histological appearance of eosinophilic infiltrate, but acute pancreatitis was rarely reported in this disease. In addition, the patient developed pancreatic pseudocyst, and delayed pseudoaneurysm hemorrhage occurred after drainage of the pseudocyst. The hemorrhage was successfully treated after angiographic embolization, and the patient remained stable after one year. The case was reported here because both the diagnosis and the management were challenging and worth learning.
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    • References (14)
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