Epidural hemangioma

硬膜外血管瘤
  • 文章类型: Case Reports
    只有罕见的同时有多个胸椎的报道,硬膜外,和先天性皮肤血管瘤发生在同一水平。
    一名24岁男性患者出现进行性轻瘫,原因是多发性椎体血管瘤(MVH)伴硬膜外扩张(即导致D1-D3显著脊髓压迫。),加上D2-D7级的先天性皮肤病变。术前血管栓塞术后,进行D1-D7椎板切除术以及C7-D8椎弓根螺钉固定.在病理上,骨和皮肤病变是脊髓海绵状血管瘤。术后,患者恢复了正常功能.因为完全切除是不可行的,他随后接受放射治疗以防止肿瘤复发。
    多层硬膜外延伸导致严重的脐带压迫和先天性皮肤损伤的MVH应尝试进行肿瘤切除,然后进行放射治疗,其中完全切除是不可行的。
    UNASSIGNED: There are only rare reports of simultaneous multiple thoracic vertebral, epidural, and congenital cutaneous hemangiomas occurring at the same levels.
    UNASSIGNED: A 24-year-old male presented with a progressive paraparesis attributed to multiple vertebral hemangiomas (MVH) with epidural extension (i.e. resulting in D1-D3 significant cord compression.), plus congenital cutaneous lesions at the D2-D7 levels. Following preoperative angioembolisation, a D1-D7 laminectomy was performed along with a C7-D8 pedicle screw fixation. Pathologically the bone and cutaneous lesions were spinal cavernous hemangiomas. Postoperatively, the patient regained normal function. As complete excision was not feasible, he subsequently received radiotherapy to prevent tumor recurrence.
    UNASSIGNED: MVH with multilevel epidural extension resulting in significant cord compression and congenital cutaneous lesions should undergo attempted tumor excision followed by radiation therapy where complete removal is not feasible.
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  • 文章类型: Journal Article
    脊髓硬膜外海绵状血管瘤是罕见的。病变模仿哑铃形神经瘤的事实使这种特殊情况变得更加独特。此外,它有一个非常独特的定位(完全硬膜外,在颈胸-C7-D1-水平)。这起案件的重要性不仅与其异常罕见有关,而且还探索了诊断途径。手术由教授进行。里卡多·卡鲁索,罗马军队医院神经外科主任,罗马萨皮恩扎大学神经外科教授,在LuigiMarrocco博士的协助下,罗马军队医院高级神经外科医生。术后恢复由VenceslaoWierzbicki医生管理,罗马军队医院高级神经外科医生。
    方法:2020年,一名71岁的男子,患有左肩胛骨区域和左前臂尺骨区域的剧烈疼痛,接受手术切除累及左侧C7-D1孔的脊髓硬膜外海绵状血管瘤.手术前,放射科医生误诊为神经瘤。
    在文献中还有其他,部分位于椎管内的血管瘤的罕见病例,部分位于孔内外。在这里介绍的案例中,鉴别诊断以及潜在的神经鞘瘤,由病变的哑铃形暗示,还应该考虑脑膜瘤的可能性。两队放射科医生检查了这些图像,我们团队的放射科医生,ValentinaMartines博士和EmanuelePiccione博士,多亏了对病变特征的仔细检查,假设硬脑膜外位置。然后分析了扫描的其他方面,以帮助指导将来对类似病变的诊断。
    结论:脊柱肿瘤影响孔,仔细检查图像可以进行准确的术前鉴别诊断,区分更常见的神经瘤和其他罕见的肿瘤,比如血管瘤.
    UNASSIGNED: Spinal epidural cavernous hemangiomas are a rare occurrence. This particular case is made even more distinctive by the fact that the lesion mimicked a dumbbell-shaped neuroma. Moreover, it had a very unique localization (wholly epidural, at cervical-thoracic -C7-D1- level). The importance of this case is linked not only to its remarkable rarity, but also to the diagnostic avenues explored. The surgery was carried out by Prof. Riccardo Caruso, Head of the Neurosurgical Department of the Military Hospital of Rome and Professor of Neurosurgery of Sapienza University of Rome, assisted by Dr. Luigi Marrocco, Senior Neurosurgeon of the Military Hospital of Rome. Postsurgical recovery was managed by Dr. Venceslao Wierzbicki, Senior Neurosurgeon of the Military Hospital of Rome.
    METHODS: In 2020, a 71 year-old man, suffering from intense pain in the left scapular region and in the ulnar area of the left forearm, underwent surgery for the removal of a spinal epidural cavernous hemangioma involving the left C7-D1 foramen. Prior to surgery, the lesion had been misdiagnosed as a neuroma by a radiologist.
    UNASSIGNED: In the Literature there are other, rare cases of hemangiomas partly located in the spinal canal, and partly located intra and extra foramen. In the case here presented, differential diagnosis as well as a potential Schwannoma, suggested by the dumbbell shape of the lesion, should have considered also the possibility of a meningioma. Two teams of radiologists examined the images, the radiologists of our team, Dr. Valentina Martines and Dr. Emanuele Piccione, thanks to a close inspection of the features of the lesion, postulated the extra-dural position. Other aspects of the scans were then analyzed to help guide future diagnosis of similar lesions.
    CONCLUSIONS: With a spinal tumor affecting the foramen, a close examination of the images allows for accurate presurgical differential diagnosis, differentiating between the more frequent neuroma and other rarer tumors, such as a hemangioma.
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  • 文章类型: Case Reports
    Hemangiomas in the spinal epidural area are very rare lesions, and most of these lesions are of the cavernous type. Only seven cases of capillary hemangiomas have been reported in the English literature, and all of these cases occurred in adulthood. Here, we report on a 17-month-old girl who presented with an inability to walk. MRI revealed an epidural mass, which was diagnosed as an epidural capillary hemangioma in the thoracic region. To our best knowledge, this case is the first epidural capillary hemangioma case to occur in childhood that has been reported.
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