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本文引用的文献

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Skull base chondrosarcoma.颅底软骨肉瘤
J Clin Neurosci. 2016 Feb;24:1-5. doi: 10.1016/j.jocn.2015.10.029. Epub 2015 Dec 24.
2
Management of tumors arising from the parapharyngeal space: A systematic review of 1,293 cases reported over 25 years.咽旁间隙肿瘤的管理:对25年间报告的1293例病例的系统评价
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Chondrosarcoma: with updates on molecular genetics.软骨肉瘤:分子遗传学新进展
Sarcoma. 2011;2011:405437. doi: 10.1155/2011/405437. Epub 2011 Feb 15.
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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 cranial base chondrosarcomas.颅底软骨肉瘤的治疗
Neurosurgery. 2006 Feb;58(2):249-55; discussion 249-55. doi: 10.1227/01.NEU.0000194834.74873.FB.
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Chondrosarcoma of the head and neck.头颈部软骨肉瘤
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Surgical management of parapharyngeal space tumors: a 10-year review.咽旁间隙肿瘤的外科治疗:一项10年回顾
Otolaryngol Head Neck Surg. 2005 Mar;132(3):401-6. doi: 10.1016/j.otohns.2004.09.062.
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Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: osteosarcoma and related tumors.骨与软组织肿瘤的细胞遗传学和分子遗传学进展:骨肉瘤及相关肿瘤
Cancer Genet Cytogenet. 2003 Aug;145(1):1-30.
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Chondrosarcomas of the head and neck.头颈部软骨肉瘤
World J Surg. 1992 Sep-Oct;16(5):1010-5; discussion 1015-6. doi: 10.1007/BF02067021.
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Prognostic factors in chondrosarcoma of bone: a clinicopathologic analysis with emphasis on histologic grading.骨软骨肉瘤的预后因素:一项侧重于组织学分级的临床病理分析
Cancer. 1977 Aug;40(2):818-31. doi: 10.1002/1097-0142(197708)40:2<818::aid-cncr2820400234>3.0.co;2-b.

咽旁间隙软骨肉瘤;起源部位成谜。

Chondrosarcoma in the Parapharyngeal Space; Site of Origin an Enigma.

作者信息

Gautam Vimmi, Panda Naresh K, Nayak Gyanaranjan, Prakash D N S

机构信息

Department of Otolaryngology, Head and Neck Surgery, Post Graduate Institute of Medical Education and Research, Chandigarh, 160012 India.

出版信息

Indian J Otolaryngol Head Neck Surg. 2022 Oct;74(Suppl 2):1826-1830. doi: 10.1007/s12070-020-01852-7. Epub 2020 Apr 13.

DOI:10.1007/s12070-020-01852-7
PMID:36452579
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9702129/
Abstract

Chondrosarcoma of the head and neck region is a rare disease, representing approximately 0.1% of all head and neck neoplasms. We present a case of a 30 year old male who presented with swelling in the right retroauricular region since 4 years. Magnetic resonance imaging and computed tomography showed lesion with its epicentre in the post styloid compartment of right parapharyngeal space with superior extent around the petrous apex. The surgical procedure considered was excision. Surgical excision was challenging in view of difficult surgical access due to close and intricate relation with neurovascular structures of head and neck and an unsual pattern of spread.

摘要

头颈部软骨肉瘤是一种罕见疾病,约占所有头颈部肿瘤的0.1%。我们报告一例30岁男性病例,该患者4年来右侧耳后区域一直肿胀。磁共振成像和计算机断层扫描显示病变位于右咽旁间隙茎突后间隙,中心部位在该间隙,向上延伸至岩尖周围。考虑的手术方式为切除。鉴于该病变与头颈部神经血管结构关系密切且复杂,手术入路困难,同时其扩散模式不寻常,手术切除具有挑战性。