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本文引用的文献

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Bone sarcomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.骨肉瘤:ESMO 诊断、治疗及随访临床实践指南
Ann Oncol. 2012 Oct;23 Suppl 7:vii100-9. doi: 10.1093/annonc/mds254.
2
A low-grade chondrosarcoma presenting as an unusual cervical mass in the hyoid bone: a case report.一例表现为舌骨处罕见颈部肿块的低级别软骨肉瘤:病例报告
J Med Case Rep. 2012 Jan 18;6:21. doi: 10.1186/1752-1947-6-21.
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Chondrosarcomas of the cervical and cervicothoracic spine: surgical management and long-term clinical outcome.颈椎和颈胸段脊柱软骨肉瘤:手术治疗及长期临床结果
J Spinal Disord Tech. 2012 Feb;25(1):1-9. doi: 10.1097/BSD.0b013e31820bb085.
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Spinal chondrosarcoma: a review.脊柱软骨肉瘤:综述
Sarcoma. 2011;2011:378957. doi: 10.1155/2011/378957. Epub 2011 Mar 8.
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Chondrosarcoma of the spine: a report of three cases and literature review.脊柱软骨肉瘤:三例报告及文献综述
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The clinical approach towards chondrosarcoma.软骨肉瘤的临床治疗方法。
Oncologist. 2008 Mar;13(3):320-9. doi: 10.1634/theoncologist.2007-0237.
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Management of primary spinal chondrosarcoma: report of two cases causing cord compression.
Arq Neuropsiquiatr. 2004 Sep;62(3B):875-8. doi: 10.1590/s0004-282x2004000500026. Epub 2004 Oct 5.
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Chondrosarcoma of the mobile spine: report on 22 cases.活动脊柱软骨肉瘤:22例报告
Spine (Phila Pa 1976). 2000 Apr 1;25(7):804-12. doi: 10.1097/00007632-200004010-00008.
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Radiotherapy of chondrosarcoma of bone.骨软骨肉瘤的放射治疗
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Chondrosarcoma in the young. A clinicopathologic analysis of 79 patients younger than 21 years of age.青少年软骨肉瘤。对79例21岁以下患者的临床病理分析。
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颈椎软骨肉瘤——罕见的恶性肿瘤:一例报告

Cervical chondrosarcoma- rare malignancy: a case report.

作者信息

Merchant Shuaib, Mohiyuddin S M Azeem, Rudrappa Satish, Deo R P, A Sagayaraj, Menon Lakshmi R

机构信息

Department of ENT and Head and Neck Surgery, Sri Devraj Urs Medical College, Tamaka Kolar, 563101 India.

Department of Spine Surgery, Manipal Hospital, Bangalore, 560017 India.

出版信息

Indian J Surg Oncol. 2014 Dec;5(4):293-6. doi: 10.1007/s13193-014-0350-3. Epub 2014 Sep 14.

DOI:10.1007/s13193-014-0350-3
PMID:25767342
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4354833/
Abstract

To highlight an uncommon bone malignancy, which presented to our institute, as a neck swelling in the supraclavicular region. A 30 year old man presented with history of swelling on the left side of neck since 1 year and numbness of left upper limb since 6 months. Magnetic Resonance Imaging of the Cervical spine & MR Angiography showed a 7.4 × 4.6 cm expansile lesion involving transverse process of C5-C7 vertebrae. As the tumour was found to be deep to the phrenic nerve & brachial plexus, a dual approach was used, anteriorly via neck incision and posteriorly via the spine. The tumour was resected & iliac crest grafted along with stabilization of the cervical spine. Patient is disease free and the cervical spine stabilized with normal movements at two and half years follow up. We need to consider tumour arising from the vertebra as a differential diagnosis for any deep seated hard neck swelling in the supraclavicular region. Even low grade malignancy of this region when resected en-bloc will have a good prognosis.

摘要

为突出我院收治的一种罕见骨恶性肿瘤,其表现为锁骨上区颈部肿胀。一名30岁男性,自1年前起出现左侧颈部肿胀,6个月来左上肢麻木。颈椎磁共振成像及磁共振血管造影显示一个7.4×4.6厘米的膨胀性病变,累及C5 - C7椎体横突。由于肿瘤位于膈神经和臂丛神经深部,采用了双入路方法,前路经颈部切口,后路经脊柱。肿瘤被切除,取自体髂嵴植骨并进行颈椎固定。患者在两年半的随访中无疾病复发,颈椎稳定且活动正常。对于锁骨上区任何深部坚硬的颈部肿胀,我们需要将源于椎体的肿瘤作为鉴别诊断。即使该区域的低级别恶性肿瘤整块切除,预后也会良好。