Chondroblastoma of the cervical-thoracic junction: global data and own experience

Mykhailo P. Komarov, Oleksii S. Nekhlopochyn, Vadim V. Verbov, Oksana H. Chernenko, Anna A. Shmelova, Ievgen V. Cheshuk, Tetiana A. Malysheva
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Abstract

Chondroblastoma (CB) ‒ a rare benign tumor of the skeleton that is presented by proliferation of chondroblasts with islands of eosinophilic chondroid matrix. CB accounts for less than 1% of all bone neoplasms, while the spine is affected in only 1.4% of all CB cases. Publications devoted to CB of the spine are sporadic and therefore have a considerable scientific interest due to the rarity of the pathology. A clinical case of CB of the cervical-thoracic junction of a 38-year-old patient hospitalized to State Institution "Romodanov Neurosurgery Institute of the National Academy of Sciences of Ukraine" in November 2022 is presented. The anamnesis shows that in 2016 a pathological fracture of the Th2 vertebral body was diagnosed. In 2017, a surgical intervention - an open biopsy of the Th2 vertebral arch was performed in a private clinic, but the histopathological analysis, due to the insufficient amount of material and the absence of clinical data, was descriptive, with a certain diagnostic number of possible nosologies. Additional treatment was not performed. When applying in 2022 to the State Institution "Romodanov Neurosurgery Institute of the National Academy of Sciences of Ukraine", significant negative dynamics were noted: a fracture of the body of the Th1 vertebra, total destruction of the body of the Th2 vertebra, a change in the signal from the body of the Th3 vertebra, which indicated its focal lesion. The surgery was performed in two stages. The first stage included a ventral corpectomy of the Th1‒Th3 vertebrae with fusion using telescopic body replacement implant and a ventral rigid plate. During the second stage laminectomy of the Th1‒Th3 vertebrae with complete resection of the Th2 costotransverse joints and partial of Th1‒Th3 ones was performed. Stabilization system screws were installed transarticularly in the facet joints C6 and C7, transpedicularly in the bodies of the Th4‒Th6 vertebrae. To increase the fusion rigidity, additional fixation of the Th1 vertebra on the right and the Th3 vertebra on the left was performed through the remaining costotransverse joints. The patient was discharged with positive neurological dynamics. The uniqueness of this case, in addition to the rarity of the histological variant of the pathology, lies in the possibility of tracking the dynamics of the disease on the basis of both neuroimaging methods and pathohistological and immunohistochemical diagnostics. Features of the prevalence of spine CB in the population, the specifiс signs when performing a spiral computer and magnetic resonance imaging, macroscopic, histological and immunohistochemical characteristics of the tumor are considered in detail. The literature data on differential diagnosis, treatment methods and prognosis of disease are organized. The material is of interest to specialists, since the timely selection of an adequate treatment method and its volume determines both the probability of tumor recurrence as well as prognosis concerning the patient’s life expectancy.
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颈胸交界处的成软骨细胞瘤:全球数据和自己的经验
成软骨细胞瘤(CB) -一种罕见的骨骼良性肿瘤,表现为成软骨细胞增生伴嗜酸性软骨样基质岛。CB占所有骨肿瘤的不到1%,而脊柱仅占所有CB病例的1.4%。致力于脊柱CB的出版物是零星的,因此由于病理学的罕见性,具有相当大的科学兴趣。报告一名38岁患者于2022年11月在“乌克兰国家科学院罗莫达诺夫神经外科研究所”住院的颈胸交界处CB临床病例。回顾显示,2016年诊断为Th2椎体病理性骨折。2017年,在一家私人诊所进行了手术干预-对Th2椎弓进行开放活检,但由于材料不足和缺乏临床数据,组织病理学分析是描述性的,具有一定的诊断数量可能的病种。未进行其他治疗。在2022年申请国立机构“乌克兰国家科学院罗莫达诺夫神经外科研究所”时,注意到明显的负面动态:Th1椎体骨折,Th2椎体完全破坏,Th3椎体信号改变,表明其局灶性病变。手术分两个阶段进行。第一阶段包括对Th1-Th3椎体进行腹侧椎体切除术,使用伸缩体置换植入物和腹侧刚性钢板进行融合。在第二阶段进行Th1-Th3椎板切除术,完全切除Th2肋横关节和部分Th1-Th3椎板。稳定系统螺钉经关节面安装在C6和C7关节面,经关节面安装在Th4-Th6椎体。为了增加融合刚度,通过剩余的肋横关节对右侧Th1椎体和左侧Th3椎体进行额外固定。患者出院时神经动力学阳性。除了罕见的病理组织学变异外,本病例的独特之处在于,在神经影像学方法和病理组织学和免疫组织化学诊断的基础上,可以跟踪疾病的动态。详细考虑了人群中脊柱CB患病率的特点,螺旋计算机和磁共振成像时的特定征象,肿瘤的宏观,组织学和免疫组织化学特征。整理本病鉴别诊断、治疗方法及预后的文献资料。专家对这些材料很感兴趣,因为及时选择适当的治疗方法及其数量决定了肿瘤复发的可能性以及与患者预期寿命有关的预后。
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