骨内古老神经鞘瘤:下颌骨一例罕见病例并文献复习。

IF 0.9 Q4 ONCOLOGY
Rare Tumors Pub Date : 2021-06-27 eCollection Date: 2021-01-01 DOI:10.1177/20363613211026480
Neda Kardouni Khoozestani, Maziar Motiee-Langroudi, Ali Salehi, Paniz Ranji
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引用次数: 6

摘要

神经鞘瘤,又称神经鞘瘤,是一种起源于雪旺细胞的良性肿瘤。古代神经鞘瘤是一种长期存在的神经鞘瘤,伴有退行性和黄瘤性变化。头颈部是神经鞘肿瘤最常见的部位之一,但累及颌骨是相当罕见的事件。我们报告一个罕见的病例骨内古老的神经鞘瘤下颌骨在24岁的男性患者最初被误诊为癌。本文讨论了其临床特征、影像学表现和治疗方案。此外,我们对9例已发表的骨内古神经鞘瘤进行了全面的文献回顾,并总结了其特征。认识各种组织病理特征的古老神经鞘瘤是必不可少的,以防止过度治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Intraosseous ancient Schwannoma: A rare case in the mandible and a literature review.

Intraosseous ancient Schwannoma: A rare case in the mandible and a literature review.

Intraosseous ancient Schwannoma: A rare case in the mandible and a literature review.

Intraosseous ancient Schwannoma: A rare case in the mandible and a literature review.

Schwannoma, otherwise known as neurilemmoma, is a benign tumor that originates from Schwann cells. Ancient Schwannoma is a long-standing Schwannoma with degenerative and xanthomatous changes. The Head and neck region is one of the most common sites for nerve sheath tumors but Involvement of the jaw is a considerably infrequent event. We report a rare case of intraosseous ancient Schwannoma of the mandible in a 24-year-old male patient which was initially misdiagnosed with carcinoma. The clinical features, radiographic findings, and treatment plan are discussed. Furthermore, a thorough literature review demonstrated nine published cases of intra-osseous ancient Schwannoma with their summarized features. Recognition of various histopathologic features of ancient Schwannoma is essential to prevent over-treatment.

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来源期刊
Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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