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原发性硬脊膜外髓外孤立性血管母细胞瘤:病例报告及系统回顾。

Primary Intradural Extramedullary Sporadic Spinal Hemangioblastomas: Case Report and Systematic Review.

机构信息

Department of Neurological Surgery, Loyola University Medical Center, Maywood, Illinois, USA.

Department of Pathology, Loyola Stritch School of Medicine, Maywood, Illinois, USA.

出版信息

World Neurosurg. 2021 Aug;152:84-94. doi: 10.1016/j.wneu.2021.05.105. Epub 2021 Jun 1.

Abstract

BACKGROUND

Hemangioblastomas are benign vascular neoplasms of the central nervous system that may occur sporadically or in association with Von Hippel-Lindau disease. A minority of these lesions can occur in the spine, mostly as intramedullary masses. The authors present a rare case of primary sporadic spinal hemangioblastoma occurring as an intradural extramedullary (IDEM) lesion. Diagnostic workup and surgical management of the patient are described.

METHODS

A systematic MEDLINE search was conducted using the keywords "hemangioblastoma" and "intradural extramedullary," "extramedullary," or "cauda equina." Clinicopathological characteristics and outcomes of the present case were reviewed and compared with those in the literature.

RESULTS

A 72-year-old man was found to have an IDEM lesion in his cervical spine after presenting with neck and shoulder pain. Gross total resection was successfully performed with sacrifice of an involved dorsal nerve rootlet. Screening for Von Hippel-Lindau was negative. Thirty-three additional patients with sporadic IDEM hemangioblastomas are reported in the literature. There was a slight male preponderance (54%) with a median age of 52 years. Patients presented with pain (54%), radiculopathy (33%), or myelopathy (32%). The majority of lesions were located in the lumbosacral spine (56%). All patients underwent maximal safe resection with stable or improved clinical status.

CONCLUSION

Primary IDEM hemangioblastomas are a rare entity. Differential diagnosis includes other IDEM lesions, such as schwannomas, meningiomas, or some vascular malformations. Resection of these sporadic tumors can be safely performed and result in improvement of neurologic deficits associated with mass effect from the tumor with low likelihood of recurrence.

摘要

背景

血管母细胞瘤是中枢神经系统的良性血管性肿瘤,可散发或与 von Hippel-Lindau 病相关。少数此类病变可发生于脊柱,主要为髓内肿块。作者报告了一例罕见的散发性脊髓血管母细胞瘤,表现为硬脊膜外(intradural extramedullary,IDEM)病变。描述了患者的诊断和手术处理方法。

方法

系统检索 MEDLINE 数据库,使用关键词“hemangioblastoma”和“intradural extramedullary”、“extramedullary”或“cauda equina”。回顾和比较了本病例的临床病理特征和结果,并与文献中的结果进行了比较。

结果

72 岁男性因颈肩部疼痛就诊,发现颈椎 IDEM 病变。成功地进行了全切除,牺牲了受累的背神经根。von Hippel-Lindau 筛查为阴性。文献中报道了 33 例散发性 IDEM 血管母细胞瘤患者。男性略多(54%),中位年龄为 52 岁。患者表现为疼痛(54%)、神经根病(33%)或脊髓病(32%)。大多数病变位于腰骶部脊柱(56%)。所有患者均接受了最大限度的安全切除,临床状况稳定或改善。

结论

原发 IDEM 血管母细胞瘤是一种罕见的实体瘤。鉴别诊断包括其他 IDEM 病变,如神经鞘瘤、脑膜瘤或某些血管畸形。这些散发性肿瘤的切除是安全的,可以改善与肿瘤占位效应相关的神经功能缺损,且复发的可能性较低。

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