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Xanthogranulomatous Epithelial Tumor: A Case Report With 1‐Year Follow‐Up

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journal contribution
submitted on 2024-12-30, 09:03 and posted on 2024-12-30, 09:04 authored by Muna AbuHejleh, Ahmed Mounir ElSayed, Renan Elsadeg Ibrahem, Asmaa Elhassan Mohamed, Adham Ammar

Summary

  • Xanthogranulomatous epithelial tumor (XGET) is a rare soft tissue and bone neoplasm with distinct immunophenotypic and molecular features.
  • The banal histomorphological characteristics of this lesion fail to foreshadow its potentially aggressive clinical behavior.
  • The prognostic and therapeutic significance is not sufficiently explored because of the rarity of this entity.

Other Information

Published in: Clinical Case Reports
License: http://creativecommons.org/licenses/by/4.0/
See article on publisher's website: https://dx.doi.org/10.1002/ccr3.9675

Funding

Open Access funding provided by the Qatar National Library.

History

Language

  • English

Publisher

Wiley

Publication Year

  • 2024

License statement

This Item is licensed under the Creative Commons Attribution 4.0 International License.

Institution affiliated with

  • Hamad Medical Corporation
  • National Center for Cancer Care and Research - HMC

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