Stenosis of the spinal canal of the thoracic spine in a patient with autosomal dominant osteopetrosis type 2

A. Vishnevskiy
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Abstract

The presented clinical observa on of a 41-year-old pa ent with an autosomal dominant form of osteopetrosis type II is interes ng not only from the point of view of the complexity of diagnosis of a rare genetic disease complicated by spinal stenosis, but also to determine the tactics of treatment. The patient was examined and treated by phthisiatricians. Histological examina on of the material obtained with trepanobiopsy showed dystrophic changes in bone tissue and poor infi ltra on with lymphocytes; data for tuberculosis of the spine was not revealed. Taking into account the pronounced neurological disorders on the background of spinal cord compression, as well as the instability of the spine, the patient was carried out pallia ve surgery (open biopsy with decompression of the spinal canal, posterior laminar fi xa on of ThVIII—LIIand anterior fi xa on of ThVIII–XIIcombined  tanium implant).  Histological examina on of tissues obtained by open biopsy allowed to suspect a rare disease and fi nally verify the diagnosis after genetic examina on.
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常染色体显性2型骨质疏松症患者的胸椎椎管狭窄
本文对一41岁常染色体显性II型骨质疏松症患者的临床观察,不仅从这种罕见遗传病合并椎管狭窄的诊断复杂性的角度来看,而且从确定治疗策略的角度来看,都是很有趣的。病人由眼科医生检查和治疗。组织切片检查显示骨组织营养不良,淋巴细胞浸润不良;脊柱结核的数据未透露。考虑到脊髓压迫背景下明显的神经系统疾病,以及脊柱的不稳定,患者进行了pallia手术(开放活检,椎管减压,thviii - liv的后椎板和thviii - xii联合钛植入物的前椎板)。对开放活检获得的组织进行组织学检查,可以怀疑是一种罕见的疾病,并在基因检查后最终证实诊断。
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