Das Kuntal Kanti, Jaiswal Sushila, Shukla Mukesh, Srivastava Arun Kumar, Behari Sanjay, Kumar Raj
Department of Neurosurgery, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Department of Pathology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
J Pediatr Neurosci. 2014 May;9(2):162-5. doi: 10.4103/1817-1745.139336.
Spinal intramedullary tuberculoma (SIT) is a rare manifestation of neurotuberculosis. Concurrent SIT and intracranial tuberculoma are further unusual. Most of these tuberculomas respond completely to medical therapy, and surgical excision is seldom required. In this report, we describe a 17-year-old boy who developed cervical intramedullary tuberculoma at C3-C6 level with a concurrent lesion involving the right cerebellar hemisphere while on treatment for tubercular meningitis. This patient had paradoxical increase in size of the cervical lesion even though the cerebellar lesion showed regression in size. In this article, we discuss the paradoxical response to anti-tubercular therapy in central nervous system tuberculosis, possible causes of nonresolution of tuberculoma on medical therapy and evaluate the role of surgery in these cases.
脊髓髓内结核瘤(SIT)是神经结核的一种罕见表现。同时存在SIT和颅内结核瘤则更为罕见。这些结核瘤大多对药物治疗有完全反应,很少需要手术切除。在本报告中,我们描述了一名17岁男孩,他在治疗结核性脑膜炎期间,在C3 - C6水平出现颈髓内结核瘤,同时右侧小脑半球有一个并发病变。尽管小脑病变大小缩小,但该患者颈部病变大小却反常增大。在本文中,我们讨论了中枢神经系统结核对抗结核治疗的反常反应、药物治疗后结核瘤未消退的可能原因,并评估了手术在这些病例中的作用。