Spinal Osteoarticular Multidrug-resistant Tuberculosis (MDR/RR-TB) in a Child: A Case Report

F. Ukunda, Mabua A Chuene
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Abstract

We report a case of a young child with multidrug-resistant tuberculosis (MDR/RR-TB) of the thoracic spine, complicated by myelopathy. Clinical assessment revealed a lower thoracic gibbus and neurological features of upper motor neuron syndrome conforming to myelopathy. Radiological evaluation revealed a marked kyphosis, contiguous T10-T11 vertebral destruction, paraspinal soft tissue collection, and intraspinal compression with cord signal changes, suggestive of spinal TB. Rapid molecular testing expedited the diagnosis of MDR/RR-TB and guided prompt treatment initiation. Although second-line drugs are the mainstay of treatment, surgery was undertaken due to marked kyphosis, spinal instability, and neurological complications in the growing spine. Although the case seems interesting, it, unfortunately, highlights multiple health system failures in developing countries, resulting in premature termination of MDR/RR-TB treatment and loss of kyphosis correction with subsequent recurrence of the kyphotic deformity.
儿童脊柱骨关节耐多药结核(MDR/RR-TB):病例报告
我们报告了一例患有胸椎耐多药结核病(MDR/RR-TB)并发脊髓病的幼儿病例。 临床评估显示,患儿胸椎下部出现胫骨后凸,并伴有符合脊髓病的上运动神经元综合征的神经特征。放射学评估显示,患者有明显的脊柱后凸、T10-T11椎体连续破坏、脊柱旁软组织聚集、椎管内压迫并伴有脊髓信号改变,提示脊柱结核。快速分子检测加快了 MDR/RR-TB 的诊断速度,并为及时开始治疗提供了指导。虽然二线药物是治疗的主要手段,但由于患者脊柱明显后凸、脊柱不稳定以及脊柱生长过程中出现神经系统并发症,因此需要进行手术治疗。 虽然这个病例看起来很有趣,但不幸的是,它凸显了发展中国家医疗系统的多种失误,导致 MDR/RR-TB 治疗过早终止,脊柱后凸矫正失败,随后畸形复发。
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