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