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本文引用的文献

1
Sacral chondroblastoma - a rare location, a rare pathology: A case report and review of literature.骶骨软骨母细胞瘤——罕见的发病部位,罕见的病理类型:一例病例报告及文献复习
World J Clin Cases. 2021 Jul 16;9(20):5709-5716. doi: 10.12998/wjcc.v9.i20.5709.
2
H3.3 K36M Mutation as a Clinical Diagnosis Method of Suspected Chondroblastoma Cases.H3.3 K36M 突变作为疑似成软骨细胞瘤病例的临床诊断方法。
Orthop Surg. 2021 Apr;13(2):616-622. doi: 10.1111/os.12878. Epub 2021 Feb 23.
3
Missed radiographic and clinical findings in a case of non-idiopathic scoliosis resulting from chondroblastoma.软骨母细胞瘤导致非特发性脊柱侧弯漏诊的影像学和临床表现。
Spine Deform. 2021 Jan;9(1):297-301. doi: 10.1007/s43390-020-00185-3. Epub 2020 Aug 21.
4
Metastasizing chondroblastoma: a rare bone tumor no longer supported by the WHO classification.转移型成软骨细胞瘤:一种罕见的骨肿瘤,不再被 WHO 分类所支持。
Skeletal Radiol. 2021 Jan;50(1):255-260. doi: 10.1007/s00256-020-03525-6. Epub 2020 Jun 27.
5
Clinicopathologic Analysis of Chondroblastoma in Adults: A Single-Institution Case Series.成人成软骨细胞瘤的临床病理分析:单机构病例系列。
Int J Surg Pathol. 2021 Apr;29(2):120-128. doi: 10.1177/1066896920927794. Epub 2020 Jun 2.
6
Chondroblastoma Of The Lumbar Vertebra.腰椎软骨母细胞瘤
J Ayub Med Coll Abbottabad. 2018 Oct-Dec;30(4):608-610.
7
Clinical features, treatments and long-term follow-up outcomes of spinal chondroblastoma: report of 13 clinical cases in a single center.脊柱成软骨细胞瘤的临床特征、治疗方法和长期随访结果:单中心 13 例临床病例报告。
J Neurooncol. 2018 Oct;140(1):99-106. doi: 10.1007/s11060-018-2935-0. Epub 2018 Jul 2.
8
Chondroblastoma of extra-craniofacial bones: Clinicopathological analyses of 103 cases.颅外面部骨骼软骨母细胞瘤:103例临床病理分析
Pathol Int. 2017 Oct;67(10):495-502. doi: 10.1111/pin.12586.
9
Intraoperative crush smear cytology of vertebral chondroblastoma: A diagnostic challenge.椎体软骨母细胞瘤的术中压片细胞学检查:一项诊断挑战。
Diagn Cytopathol. 2018 Jan;46(1):79-82. doi: 10.1002/dc.23799. Epub 2017 Aug 23.
10
Chondroblastoma in adult age.成人期软骨母细胞瘤
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胸椎软骨母细胞瘤:一例报告并文献复习

Chondroblastoma of Thoracic Vertebrae: a Case Report and Review of the Literature.

作者信息

Tabibkhooei Alireza, Javadnia Parisa

机构信息

Department of Neurosurgery, Iran University of Medical Sciences, Tehran, Iran.

出版信息

Indian J Surg Oncol. 2024 Mar;15(Suppl 1):22-28. doi: 10.1007/s13193-022-01659-8. Epub 2022 Oct 13.

DOI:10.1007/s13193-022-01659-8
PMID:38545582
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10963700/
Abstract

Chondroblastoma is a rare benign cartilaginous bone tumor typically seen at the epiphysis of long axial bones. In this regard, there are rare findings about spinal chondroblastomas. We report a 29-year-old man with T1 vertebral chondroblastoma misdiagnosed with a traumatic fracture following an accident. The patient was admitted to our clinic with a chief complaint of axial back pain and kyphosis following posterior spinal fixation. We report his clinical and imaging data before his past operation and at this admission. Our patient underwent a two-stage operation. In the first stage, posterior spinal reconstruction and kyphosis correction was performed. In the second stage, mass resection was performed anteriorly in the T1 vertebral body as much as possible. The results confirmed the chondroblastoma diagnosis histologically. Our patient remained symptom-free with no growth in tumor remnant during 6 months follow-up. Although vertebral chondroblastoma is a sporadic tumor, it should be considered in the differential diagnosis when facing a vertebral infiltrative osteolytic mass, even when mimicking a traumatic fracture after the accident. In addition, histological confirmation is necessary under such conditions. We also reviewed the literature's clinical presentations, imaging findings, and treatments of 34 case reports with vertebral chondroblastoma.

摘要

软骨母细胞瘤是一种罕见的良性软骨性骨肿瘤,通常见于长轴骨的骨骺。在这方面,关于脊柱软骨母细胞瘤的报道很少。我们报告一例29岁男性,其T1椎体软骨母细胞瘤在一次事故后被误诊为创伤性骨折。该患者因脊柱后路固定术后轴向背痛和脊柱后凸为主诉入院。我们报告了他上次手术前及此次入院时的临床和影像学资料。我们的患者接受了两阶段手术。第一阶段,进行了脊柱后路重建和脊柱后凸矫正。第二阶段,尽可能在T1椎体前方进行肿物切除。结果经组织学证实为软骨母细胞瘤。我们的患者在6个月的随访期间无症状,肿瘤残余无生长。尽管椎体软骨母细胞瘤是一种散发性肿瘤,但当面对椎体浸润性溶骨性肿物时,即使其在事故后类似创伤性骨折,在鉴别诊断中也应考虑到它。此外,在这种情况下组织学确诊是必要的。我们还回顾了34例椎体软骨母细胞瘤病例报告的文献中的临床表现、影像学表现及治疗方法。