一例罕见的脊索瘤表现为Pancoast肿瘤。

IF 0.9 Q4 ONCOLOGY Rare Tumors Pub Date : 2021-07-02 eCollection Date: 2021-01-01 DOI:10.1177/20363613211029493
Philip T Sobash, Krishna Vedala, Daniel Alfano, Heather Pinckard-Dover, Jason L Muesse, Raman Desikan
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引用次数: 0

摘要

脊索是所有脊索动物胚胎的决定性结构。它是外胚层、神经板和神经弓腹侧的中线结构。脊索的残余最终形成髓核。脊索的功能是组织周围的结构。脊索瘤是一种罕见的恶性骨肿瘤,起源于脊索的残余。这些肿瘤是无痛的,可表现为偶发或局部进展,累及邻近结构。这些肿瘤通常出现在颅底和骶骨,但很少出现在颈椎和胸椎。有罕见的脊索瘤侵袭臂丛的病例记录。手术切除是脊索瘤的主要治疗方法。我们将讨论脊索瘤作为Pancoast肿瘤的一种新表现,并旨在强调准确诊断和计划治疗的临床重要性,以及不完全手术切除的不良预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A rare case of chordoma presenting as a Pancoast tumor.

The notochord is the defining structure of all chordate embryos. It is a midline structure ventral to the ectoderm, neural plates, and neural arch. Remnants of the notochord ultimately give rise to the nucleus pulposus. The function of the notochord is to organize the surrounding structures. Chordoma is a rare malignant bone tumor arising from remnants of the notochord. These tumors are indolent and can present as incidental or locally advanced involving adjacent structures. These tumors typically present at the skull base and sacral spine but more rarely can be seen on the cervical and thoracic spine. Rare cases of chordoma invading the brachial plexus have been recorded. Surgical resection is the mainstay of treatment for chordomas. We would like to discuss a novel presentation of a chordoma as a Pancoast tumor, and aim to highlight the clinical importance of accurate diagnosis and planning therapy along with poor prognosis of incomplete surgical resection.

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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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