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锁骨尤文肉瘤:病例系列。

Ewing sarcoma of the clavicle: a case series.

机构信息

Department of Medical Oncology, Dr BRA Institute Rotary Cancer Hospital, AIIMS, New Delhi 110 029, India.

出版信息

Indian Pediatr. 2011 Feb;48(2):133-4. doi: 10.1007/s13312-011-0038-5. Epub 2010 Nov 30.

DOI:10.1007/s13312-011-0038-5
PMID:21169648
Abstract

Clavicle is a rare primary site for Ewing sarcoma (ES). We analyzed 4 patients with clavicular ES under our follow up and reviewed the literature on management of this rare tumor. All our patients were females with a median age of 16 years and were non metastatic at presentation. After a median follow-up of 21.5 months, 3 out of 4 patients are in complete remission. Clavicular ES in contrast to ES of other sites seems to have a female preponderance and outcomes are similar to non metastatic ES of other common sites.

摘要

锁骨是尤文肉瘤(ES)的罕见原发部位。我们分析了在随访中 4 例锁骨 ES 患者,并复习了关于这种罕见肿瘤治疗的文献。我们所有的患者均为女性,中位年龄 16 岁,初诊时无转移。中位随访 21.5 个月后,4 例患者中的 3 例完全缓解。与其他部位的 ES 相比,锁骨 ES 似乎女性发病倾向更高,且预后与其他常见部位无转移的 ES 相似。

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引用本文的文献

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A Rare Case of Mid-clavicular Ewing Sarcoma Treated With Total Claviculectomy: A Case Report and Literature Review.1例采用全锁骨切除术治疗的锁骨中段尤因肉瘤罕见病例:病例报告及文献综述
Cureus. 2025 Feb 14;17(2):e78979. doi: 10.7759/cureus.78979. eCollection 2025 Feb.
2
Comprehensive Management of Distal Clavicle Ewing's Sarcoma: A Case Highlighting Surgical Resection, Oncologic Challenges, and Rehabilitation Outcomes.锁骨远端尤因肉瘤的综合管理:一个突出手术切除、肿瘤学挑战及康复结果的病例
Cureus. 2024 Aug 14;16(8):e66901. doi: 10.7759/cureus.66901. eCollection 2024 Aug.