젊은 성인에서 발생한 자발성 흉추 경막외 혈종 - 증례 보고 -Spontaneous Spinal Epidural Hematoma of the Thoracic Spine in Young Adult - A Case Report
- Other Titles
- Spontaneous Spinal Epidural Hematoma of the Thoracic Spine in Young Adult - A Case Report
- Authors
- 정순택; 김동희; 조세현; 남대철
- Issue Date
- 2008
- Publisher
- 대한척추외과학회
- Keywords
- Spontaneous spinal epidural hematoma (SSEH); Thoracic spine; Young adult; Operative treatment; 자발성 경막외 혈종; 흉추; 젊은 성인; 수술적 치료
- Citation
- 대한척추외과학회지, v.15, no.3, pp 194 - 198
- Pages
- 5
- Indexed
- KCICANDI
- Journal Title
- 대한척추외과학회지
- Volume
- 15
- Number
- 3
- Start Page
- 194
- End Page
- 198
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/27808
- ISSN
- 2093-4378
2093-4386
- Abstract
- A spontaneous spinal epidural hematoma (SSEH) of the thoracic spine is a rare space-occupying disease that accompanied with
severe axial pain in the spine. Because there is the possibility of a significant neurological injury such as paraplegia, SSEH
requires careful diagnosis and management. A SSEH is mainly caused by a coagulating disorder or anticoagulant medication,
while certain cases have shown that this disease is related with spinal inflammatory conditions. A SSEH tends to occur in
patients who have risk factors for hemorrhage. However, the incidence of SSEH is quite low, and there are few domestic reports
of a SSEH in young adults who are without the risk factors for hemorrhage. We encountered a 25 years old young male without
a prior significant medical history and he was suffering from severe back pain and paraplegia due to a SSEH at the thoracic
spine. The early diagnosis was made via MRI. We report here on a favorable clinical outcome that was achieved with immediate
operative treatment, and we include a review of the relevant literature.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - College of Medicine > Department of Medicine > Journal Articles

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.