دوشنبه 27 بهمن 1404
دوره 12، شماره 1 - ( 10-1404 )
جلد 12 شماره 1 صفحات 86-80 |
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Ethics code: Ethics approval was not required for this case report. However, written informed consent was obtaine
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Bhuwana Putra M, Muhammad Rosyidi R, Priyanto B, Monica M, Gde Bagus Mahadewa T, Niryana I W, et al . Spinal Epidural Arachnoid Cyst: Case Report and Literature Review. Caspian J Neurol Sci 2026; 12 (1) :80-86
URL: http://cjns.gums.ac.ir/article-1-775-fa.html
URL: http://cjns.gums.ac.ir/article-1-775-fa.html
Spinal Epidural Arachnoid Cyst: Case Report and Literature Review. مجله علوم اعصاب کاسپین. 1404; 12 (1) :80-86
چکیده: (18 مشاهده)
Background: Spinal epidural arachnoid cysts (SEACs) are rare, accounting for ~1% of all spinal tumors. While often incidental, large cysts may compress nerve roots or the spinal cord, leading to motor or sensory deficits. The etiology and pathophysiology of these conditions remain unclear, and no standardized management guidelines exist. Surgical treatment is indicated for symptomatic cases, with dural defect repair essential to prevent recurrence.
Case Description: A 25-year-old female presented with paraparesis and intermittent leg pain of one month’s duration. Thoracolumbar magnetic resonance imaging revealed a cystic lesion extending from T11 to L1 with T2 hyperintensity similar to cerebrospinal fluid (CSF). She underwent hemilaminectomy with complete cyst resection and dural defect repair. Postoperatively, the patient demonstrated progressive neurological recovery without complications.
Conclusion: SEACs are rare lesions that may cause significant neurological symptoms if untreated. For symptomatic cases, complete cyst excision with dural repair is the preferred management to prevent recurrence and achieve favorable outcomes.
Case Description: A 25-year-old female presented with paraparesis and intermittent leg pain of one month’s duration. Thoracolumbar magnetic resonance imaging revealed a cystic lesion extending from T11 to L1 with T2 hyperintensity similar to cerebrospinal fluid (CSF). She underwent hemilaminectomy with complete cyst resection and dural defect repair. Postoperatively, the patient demonstrated progressive neurological recovery without complications.
Conclusion: SEACs are rare lesions that may cause significant neurological symptoms if untreated. For symptomatic cases, complete cyst excision with dural repair is the preferred management to prevent recurrence and achieve favorable outcomes.
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دریافت: 1403/11/16 | پذیرش: 1404/8/14 | انتشار: 1404/10/21
دریافت: 1403/11/16 | پذیرش: 1404/8/14 | انتشار: 1404/10/21
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