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...
محفوظ في:
| المؤلف الرئيسي: | |
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| مؤلفون آخرون: | , , , |
| منشور في: |
2024
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| 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> |
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