睾丸精原细胞瘤放射治疗40年后脊髓硬膜内原发性恶性周围神经鞘肿瘤的发生。

IF 0.9 Q4 CLINICAL NEUROLOGY
Case Reports in Neurological Medicine Pub Date : 2020-01-27 eCollection Date: 2020-01-01 DOI:10.1155/2020/1792582
Osmond C Wu, Berje H Shammassian, Arunit J S Chugh, Aparna Harbhajanka, Manish K Kasliwal
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引用次数: 4

摘要

摘要原发性硬膜内恶性周围神经鞘瘤是一种极为罕见的肿瘤,且预后极差。据报道,一名77岁的男性在接受睾丸精原细胞瘤放射治疗40多年后,被诊断为硬膜内MPNST。脊髓硬膜内mpnst在神经纤维瘤病之外的情况极为罕见,在影像学上可以伪装成常见的良性神经鞘肿瘤。年龄较大,症状持续时间短,且在治疗领域有过包括脊柱的局部放射治疗,无论距离远近,都应该提醒肿瘤学家和神经外科医生注意这种罕见的侵袭性肿瘤的可能存在,因为这种肿瘤的处理和总体预后与通常的硬膜内脊柱肿瘤明显不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ominous Occurrence of Spinal Intradural Primary Malignant Peripheral Nerve Sheath Tumor Four Decades following Radiation Therapy for Testicular Seminoma.

Ominous Occurrence of Spinal Intradural Primary Malignant Peripheral Nerve Sheath Tumor Four Decades following Radiation Therapy for Testicular Seminoma.

Ominous Occurrence of Spinal Intradural Primary Malignant Peripheral Nerve Sheath Tumor Four Decades following Radiation Therapy for Testicular Seminoma.

Ominous Occurrence of Spinal Intradural Primary Malignant Peripheral Nerve Sheath Tumor Four Decades following Radiation Therapy for Testicular Seminoma.

Primary intradural malignant peripheral nerve sheath tumor (MPNST) is an extremely rare diagnosis and is associated with an extremely poor prognosis. A 77-year-old man diagnosed with an intradural MPNST, more than 40 years after radiation for a testicular seminoma, is reported. Intradural MPNSTs of the spine outside the setting of neurofibromatosis is extremely rare and can masquerade as common benign nerve sheath tumors, on imaging. An older age at presentation with short duration of symptoms and prior regional radiation treatment encompassing the spine in the treatment field regardless of remoteness should alert the oncologists and neurosurgeons to the possible existence of this rare and aggressive tumor, as the management, and overall prognosis of this tumor is distinctly different compared to the usual intradural spinal tumors.

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