孤立性胸腔硬膜外表皮样囊肿:技术说明

Q3 Medicine
Malak El Marrakchi, Mostafa Haddi, Nahla Zian, Younes Bellihi, Houssine Ghannane, S. A. Benali
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引用次数: 0

摘要

先天性、后天性和先天性脊髓表皮样囊肿(EC)都非常罕见。一名62岁的女性患者因T7水平后方压迫性硬膜外病变导致进行性截瘫5个月。组织病理学证实该病变为表皮样囊肿。虽然她的痉挛症状在5周内得到了改善,但她仅恢复了部分下肢运动功能(即3/5的运动功能)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolated thoracic intradural extramedullary epidermoid cyst: A technical note
Congenital, acquired, and iatrogenic spinal epidermoid cysts (EC) are very rare. A 62-year-old female patient presented with a 5-month history of progressive paraparesis leading to paraplegia secondary to a posterior compressive intradural extramedullary lesion at the T7 level. The patient underwent a laminectomy/durotomy for gross total tumor excision. Histopathology confirmed the lesion was an epidermoid cyst. Although her spasticity improved within 5 weeks, she only regained partial lower extremity motion (i.e., 3/5 motor function). Patients presenting with the acute/subacute onset of paraparesis secondary to spinal EC should undergo timely gross total cyst resections to optimize neurological outcomes.
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CiteScore
1.30
自引率
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623
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