Literature DB >> 34387630

Juvenile Xanthogranuloma of the Pancreas in a Pediatric Patient Mimicking Pancreatic Neoplasm With High CA 19-9: Case Report and Literature Review.

Eman Al-Antary1, Avanti Gupte1, Janet Poulik2, Justin Klein3, Hamza S Gorsi1.   

Abstract

Juvenile xanthogranuloma (JXG) is a rare, non-Langerhans cell histiocytosis. It is usually a benign and self-limiting condition. The most common sites are skin and soft tissue. Pancreatic involvement is extremely rare. We present an unusual case of a 13-month-old female child with JXG of the pancreas and elevated cancer antigen 19-9. JXG should always be considered as a differential diagnosis for pediatric patients presenting with a pancreatic mass, solid and/or cystic in nature. Therefore, avoiding unnecessary invasive diagnostic procedures.
Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.

Entities:  

Mesh:

Year:  2022        PMID: 34387630     DOI: 10.1097/MPH.0000000000002279

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  1 in total

Review 1.  Pancreatic involvement in Erdheim-Chester disease: a case report and review of the literature.

Authors:  Jia-Wen Dai; Tian-Hua He; Ming-Hui Duan; Yue Li; Xin-Xin Cao
Journal:  BMC Gastroenterol       Date:  2022-06-21       Impact factor: 2.847

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.