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以脊髓压迫为表现的原发性内胚窦瘤。病例报告。

Primary endodermal sinus tumor presenting with spinal cord compression. Case report.

作者信息

Resnick D K, McLaughlin M R, Albright A L

机构信息

Department of Neurological Surgery, University of Pittsburgh School of Medicine, Children's Hospital of Pittsburgh, Pennsylvania, USA.

出版信息

J Neurosurg. 1997 Jan;86(1):151-3. doi: 10.3171/jns.1997.86.1.0151.

DOI:10.3171/jns.1997.86.1.0151
PMID:8988094
Abstract

Endodermal sinus tumor is an uncommon malignant germ-cell neoplasm. These tumors usually present in childhood or young adulthood as testicular or ovarian masses; however, mediastinal and intracranial tumors have been described. The authors report the occurrence of a primary paraspinal endodermal sinus tumor in a 21-month-old boy who presented with thoracic spinal cord compression. A review of the literature failed to reveal a similar case. The clinical presentation, radiographic characteristics, operative findings, and patient outcome are discussed.

摘要

内胚窦瘤是一种罕见的恶性生殖细胞肿瘤。这些肿瘤通常在儿童期或青年期表现为睾丸或卵巢肿块;然而,也有纵隔和颅内肿瘤的报道。作者报告了一名21个月大的男孩发生原发性脊柱旁内胚窦瘤,该患儿出现胸段脊髓受压。文献回顾未发现类似病例。本文讨论了其临床表现、影像学特征、手术所见及患者预后。

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引用本文的文献

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Metastatic epidural spinal cord compression from testicular yolk sac tumor: case report and literature review.睾丸卵黄囊瘤致转移性硬膜外脊髓压迫症:病例报告及文献复习
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Successful treatment of a primary thoracic dumb-bell yolk sac tumor presenting with severe spinal cord compression: Case report.成功治疗伴有严重脊髓压迫的原发性胸段哑铃型卵黄囊瘤:病例报告
Medicine (Baltimore). 2019 Oct;98(43):e17610. doi: 10.1097/MD.0000000000017610.
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Rare case of conus medullaris syndrome from a metastatic yolk sac tumor originating from the mediastinum of an adult male: a case report and review of the literature.
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Int J Spine Surg. 2015 Nov 6;9:59. doi: 10.14444/2059. eCollection 2015.
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Metastatic sacrococcygeal yolk sac tumor: A misleading diagnosis.转移性骶尾部卵黄囊瘤:一种具有误导性的诊断。
J Neurosci Rural Pract. 2015 Jul-Sep;6(3):395-8. doi: 10.4103/0976-3147.158772.