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JCR 2016
جستجوی مقالات
شنبه 22 آذر 1404
Iranian Journal of Medical Sciences
، جلد ۴۴، شماره ۳، صفحات ۲۵۱-۰
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
Spontaneous Resolution of Symptomatic Thoracic Spine Calcified Disc Herniation: A Case Report and Literature Review
چکیده انگلیسی مقاله
Calcification of intervertebral disc (IVD) is an uncommon but well-defined clinical syndrome in children. Despite its benign nature, occasionally, calcified nucleus pulposus can herniate into the spinal canal. We report an interesting case of calcified disc herniation in the thoracic spine. Although it resulted in cord compression and syrinx formation, it well responded to conservative management. An 8-year-old girl presented with back pain and lower limbs hyperreflexia. The spinal imaging revealed that calcification within IVD, associated with huge calcified disc herniation on the T5/6, resulted in cord compression and syrinx formation within the spinal cord from T4/5 through T9/10. Despite cord compression and syrinx formation, the patient underwent conservative management. After a 6-month follow-up, the control imaging showed complete resolution of the calcified disc herniation and decreased syrinx size. In the patients with a calcified herniated IVD, in the absence of motor neurological deficit, conservative management consisting of bed rest, lifestyle adjustment, weight loss, and brace or collar wearing combined with a close follow-up can result in spontaneous regression of calcification, improvement of symptoms, and partial to complete resolution of the underlying pathology.
کلیدواژههای انگلیسی مقاله
نویسندگان مقاله
| Ali Babashahi
Department of Neurosurgery, Iran University of Medical Sciences, Tehran, Iran
| Morteza Taheri
Department of Radiology, Lar University of Medical Sciences, Fars, Iran
| Parham Rabiee
نشانی اینترنتی
http://ijms.sums.ac.ir/index.php/IJMS/article/view/4665
فایل مقاله
اشکال در دسترسی به فایل - ./files/site1/rds_journals/147/article-147-1464470.pdf
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زبان مقاله منتشر شده
en
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نوع مقاله منتشر شده
Case Report(s)
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