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

<h3>Summary</h3><ul><li>Xanthogranulomatous epithelial tumor (XGET) is a rare soft tissue and bone neoplasm with distinct immunophenotypic and molecular features.</li><li>The banal histomorphological characteristics of this lesion fail to foreshadow its potentiall...

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محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: Muna AbuHejleh (20484011) (author)
مؤلفون آخرون: Ahmed Mounir ElSayed (14777314) (author), Renan Elsadeg Ibrahem (20484014) (author), Asmaa Elhassan Mohamed (20484017) (author), Adham Ammar (14151933) (author)
منشور في: 2024
الموضوعات:
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الوصف
الملخص:<h3>Summary</h3><ul><li>Xanthogranulomatous epithelial tumor (XGET) is a rare soft tissue and bone neoplasm with distinct immunophenotypic and molecular features.</li><li>The banal histomorphological characteristics of this lesion fail to foreshadow its potentially aggressive clinical behavior.</li><li>The prognostic and therapeutic significance is not sufficiently explored because of the rarity of this entity.</li></ul><h2>Other Information</h2><p dir="ltr">Published in: Clinical Case Reports<br>License: <a href="http://creativecommons.org/licenses/by/4.0/" target="_blank">http://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.1002/ccr3.9675" target="_blank">https://dx.doi.org/10.1002/ccr3.9675</a></p>