ArticleJournal of oral and maxillofacial pathology : JOMFP2018
Aggressive high-grade Ewing's sarcoma of maxilla: A rare case report.
Article in Journal of oral and maxillofacial pathology : JOMFP, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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3 citing papers in PubMed, 12 citations in OpenAlex.
- Ewing sarcoma of the facial soft tissues-a case report.Journal of surgical case reports · 2022Article
- A rare case of Ewing sarcoma metastasis to the oral cavity.Imaging science in dentistry · 2021Article
- A Case of Ewing Sarcoma of the Mandible onAsia Oceania journal of nuclear medicine & biology · 2020Article
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4 authors at 2 institutions in 1 country.
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Abstract
Ewing's sarcoma (ES) is an uncommon malignancy of childhood and adults that constitutes 6%-8% of all primary malignant tumors and the third-most common tumor after osteosarcoma and chondrosarcoma, frequently involves the mandible among jaw bones. This article presents a rare case of ES of maxilla in a 22-year-old male patient showing extensive lesion into skull base which was confirmed with computed tomography, dilemmatic histopathologic features in H and E which is not a frequent presentation. Histopathologic features showed monotonous round cells with hypo- and hyper-cellular areas, intralesional hemorrhage and necrosis with lesional cells positive for CD99. Although the prognosis is poor, early diagnosis and long-term follow-up can improve the survival. The diagnosis was confirmed by immunohistochemistry where lesional cells were positive for CD 99 and vimentin. ES of maxilla is a rare and aggressive tumor. Hence, early diagnosis, combined therapy, and long-term follow-up are suggested in such cases.
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