头颈部畸胎瘤肉瘤:一种罕见实体的临床病理回顾。

IF 0.9 Q4 ONCOLOGY
Rare Tumors Pub Date : 2023-09-21 eCollection Date: 2023-01-01 DOI:10.1177/20363613231204047
Rana S Al-Zaidi
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引用次数: 0

摘要

畸胎瘤是一种罕见的、高度侵袭性的头颈部恶性肿瘤,其特征是上皮、间充质和原始神经上皮细胞的多表型和三相生长。由于畸胎癌肉瘤的罕见性和形态异质性,以及缺乏这种肿瘤的经验,它经常被误诊,尤其是在小的活检样本中,当只确定了一些成分时,从而导致治疗延迟。积极的临床行为和不良的生存结果,需要准确的诊断和适当的治疗。这篇综述描述了畸胎癌肉瘤的主要人口统计学和临床病理特征,并强调了试图确定该肿瘤分子特征的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Teratocarcinosarcoma of the head and neck: Clinicopathologic review of a rare entity.

Teratocarcinosarcoma of the head and neck: Clinicopathologic review of a rare entity.

Teratocarcinosarcoma of the head and neck: Clinicopathologic review of a rare entity.

Teratocarcinosarcoma of the head and neck: Clinicopathologic review of a rare entity.

Teratocarcinosarcoma is a rare, highly aggressive malignancy of the head and neck, characterized by multiphenotypic and triphasic growth of epithelial, mesenchymal, and primitive neuroepithelial elements. Owing to its rarity and morphological heterogeneity, as well as the lack of experience with this neoplasm, teratocarcinosarcoma is often misdiagnosed, particularly in small biopsy samples when only some of the elements are identified, thus leading to delayed management. Aggressive clinical behavior and poor survival outcomes, necessitate an accurate diagnosis and appropriate treatment. This review describes the main demographic and clinicopathological features of teratocarcinosarcoma, with an emphasis on the recent advances that have attempted to identify the molecular signature of this neoplasm.

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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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