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获得性Chiari I型畸形和脊髓空洞症伴双侧慢性硬膜下血肿。病例报告。

Acquired Chiari I malformation and syringomyelia associated with bilateral chronic subdural hematoma. Case report.

作者信息

Morioka T, Shono T, Nishio S, Yoshida K, Hasuo K, Fukui M

机构信息

Department of Neurosurgery, Kyushu University, Fukuoka, Japan.

出版信息

J Neurosurg. 1995 Sep;83(3):556-8. doi: 10.3171/jns.1995.83.3.0556.

Abstract

The authors report a case of bilateral chronic subdural hematoma in a 25-year-old woman who had occipital and neck pain. Magnetic resonance imaging revealed progressive caudal descent of the cerebellar tonsils (acquired Chiari I malformation) and a large eccentric syrinx in the spinal cord from the C3-T7 levels. Spontaneous disappearance of the chronic subdural hematomas resulted in radiographic resolution of both lesions, as well as clinical improvement. Theories of syringomyelia formation, the relationship to acquired Chiari I malformation, and the implications of this case are discussed.

摘要

作者报告了一例25岁女性双侧慢性硬膜下血肿病例,该患者伴有枕部和颈部疼痛。磁共振成像显示小脑扁桃体进行性尾端下移(获得性Chiari I畸形)以及脊髓C3 - T7节段有一个大的偏心空洞。慢性硬膜下血肿的自发消失导致两个病变在影像学上消退,同时临床症状也有所改善。本文讨论了脊髓空洞症形成的理论、与获得性Chiari I畸形的关系以及该病例的意义。

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