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儿童孤立性脊髓硬膜外海绵状血管瘤的急性表现

Acute presentation of solitary spinal epidural cavernous angioma in a child.

作者信息

Khalatbari Mahmoud Reza, Hamidi Mehrdokht, Moharamzad Yashar

机构信息

Department of Neurosurgery, Arad Hospital, Tehran, Iran.

出版信息

J Coll Physicians Surg Pak. 2013 May;23(5):364-6.

Abstract

Solitary spinal epidural cavernous angiomas are rare lesions, especially in paediatric age group. They are infrequently considered in the differential diagnosis of spinal epidural masses in children. We report a case of solitary epidural cavernous angioma of the thoracic spine in a child presenting with acute onset of back pain and myelopathy. Magnetic resonance imaging of the thoracic spine demonstrated a posterior epidural mass at T6-T8 levels with compression of the spinal cord. Using microsurgical technique and bipolar coagulation, total excision of the lesion was achieved. Histopathological examination confirmed the diagnosis of cavernous angioma. At the five-year follow-up, there was no recurrence of the tumour.

摘要

孤立性脊柱硬膜外海绵状血管瘤是罕见的病变,尤其是在儿童年龄组。在儿童脊柱硬膜外肿块的鉴别诊断中很少考虑到它们。我们报告一例儿童胸椎孤立性硬膜外海绵状血管瘤,表现为急性背痛和脊髓病。胸椎磁共振成像显示T6 - T8水平有一个硬膜外后肿块,压迫脊髓。采用显微外科技术和双极电凝,实现了病变的完全切除。组织病理学检查证实为海绵状血管瘤。在五年随访中,肿瘤无复发。

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