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本文引用的文献

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Spinal intradural capillary haemangioma: a review.脊髓硬膜内毛细血管瘤:综述
Eur Spine J. 2001 Dec;10(6):464-72. doi: 10.1007/s005860100296.
2
Spinal intradural extramedullary capillary hemangioma: MR imaging findings.脊髓硬膜内髓外毛细血管瘤:磁共振成像表现
AJNR Am J Neuroradiol. 2001 Apr;22(4):799-802.
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Capillary hemangioma of the spinal cord. Report of four cases.脊髓毛细血管瘤。4例报告。
J Neurosurg. 2000 Jul;93(1 Suppl):148-51. doi: 10.3171/spi.2000.93.1.0148.
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Spinal intradural capillary hemangioma: MR findings.脊髓硬膜内毛细血管瘤:磁共振成像表现
AJNR Am J Neuroradiol. 2000 May;21(5):954-6.
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Hemangioma of spinal nerve root.脊神经根血管瘤。
J Neurosurg. 1999 Oct;91(2 Suppl):175-80. doi: 10.3171/spi.1999.91.2.0175.
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Lobular capillary hemangioma of the cauda equina. Case report.马尾神经的小叶状毛细血管瘤。病例报告。
J Neurosurg. 1999 Apr;90(2 Suppl):239-41. doi: 10.3171/spi.1999.90.2.0239.
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Intramedullary disseminated capillary hemangioma with localized spinal cord swelling: case report.
Neurosurgery. 1993 Dec;33(6):1099-101. doi: 10.1227/00006123-199312000-00020.
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Giant congenital capillary hemangioma of pericranium--case report.巨大先天性颅骨膜毛细血管血管瘤——病例报告
Neurol Med Chir (Tokyo). 1990 Dec;30(13):1029-33. doi: 10.2176/nmc.30.1029.

硬脊膜内髓外毛细血管瘤:一例报告并文献复习

Intradural extramedullary capillary hemangioma: A case report and review of the literature.

作者信息

Zhu Kejun, He Dengwei

机构信息

Department of Spinal Surgery, Lishui Center Hospital, Zhejiang University, Lishui, Zhejiang 323000, P.R. China.

出版信息

Oncol Lett. 2016 Apr;11(4):2896-2898. doi: 10.3892/ol.2016.4320. Epub 2016 Mar 9.

DOI:10.3892/ol.2016.4320
PMID:27073572
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4812146/
Abstract

Capillary hemangiomas are benign tumors frequently located in the skin and other soft tissues during childhood. However, intradural extramedullary capillary hemangioma is extremely rare. The current study reports a rare case of intradural extramedullary capillary in a 59-year-old woman who presented with backache and right lower limb numbness that had progressed over 20 days. Magnetic resonance imaging of the thoracic spine showed an ill-defined mass at the T8 level. All other examinations were normal. The patient underwent surgery and recovered successfully. Histopathological examinations showed that the tumor exhibited the typical histological findings of capillary hemangioma, as it was comprised of a proliferation of capillary-sized vessels. The patient remains alive with no evidence of tumor metastasis and recurrence at 24 months post-surgery.

摘要

毛细血管瘤是一种良性肿瘤,在儿童时期常位于皮肤和其他软组织中。然而,硬脊膜内髓外毛细血管瘤极为罕见。本研究报告了一例罕见的59岁女性硬脊膜内髓外毛细血管瘤病例,该患者出现背痛和右下肢麻木症状,持续20天且逐渐加重。胸椎磁共振成像显示T8水平有一个边界不清的肿块。其他所有检查均正常。患者接受手术并成功康复。组织病理学检查显示,肿瘤呈现毛细血管瘤典型的组织学特征,由大量毛细血管大小的血管增生构成。术后24个月,患者存活,无肿瘤转移和复发迹象。