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BMJ Case Rep. 2017 Jun 22;2017:bcr-2017-219722. doi: 10.1136/bcr-2017-219722.
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Establishment and characterization of novel patient-derived extraskeletal osteosarcoma cell line NCC-ESOS1-C1.新型患者来源的 extraskeletal 骨肉瘤细胞系 NCC-ESOS1-C1 的建立与鉴定。
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本文引用的文献

1
The Treatment and Outcomes of Extraskeletal Osteosarcoma: Institutional Experience and Review of The Literature.骨外骨肉瘤的治疗与预后:机构经验及文献综述
Iowa Orthop J. 2016;36:98-103.
2
Extraskeletal osteosarcoma: a case report and review of the literature.骨外骨肉瘤:一例病例报告及文献综述
J Radiol Case Rep. 2013 Jul 1;7(7):15-23. doi: 10.3941/jrcr.v7i7.1245. eCollection 2013 Jul.
3
Extraskeletal Osteosarcoma: An International Rare Cancer Network Study.骨外骨肉瘤:一项国际罕见癌症网络研究。
Am J Clin Oncol. 2016 Feb;39(1):32-6. doi: 10.1097/COC.0000000000000005.
4
Extraosseous osteosarcoma in Ibadan: case series over a 20-year period.伊巴丹的骨外骨肉瘤:20年病例系列
Rare Tumors. 2009 Jul 22;1(1):e3. doi: 10.4081/rt.2009.e3.
5
Extraskeletal osteosarcoma: analysis of outcome of a rare neoplasm.骨外骨肉瘤:一种罕见肿瘤的预后分析
Sarcoma. 2000;4(3):119-23. doi: 10.1080/13577140020008084.
6
EXTRASKELETAL OSSIFYING TUMORS.骨外骨化性肿瘤
Ann Surg. 1941 Jan;113(1):95-112. doi: 10.1097/00000658-194101000-00013.
7
Extraosseous osteogenic sarcoma.骨外骨肉瘤
J Chin Med Assoc. 2005 Nov;68(11):542-5. doi: 10.1016/s1726-4901(09)70091-7.
8
Extraosseous osteosarcoma: response to treatment and long-term outcome.骨外骨肉瘤:治疗反应及长期预后
J Clin Oncol. 2002 Jan 15;20(2):521-7. doi: 10.1200/JCO.2002.20.2.521.
9
Osteocalcin and osteonectin immunoreactivity in extraskeletal osteosarcoma: a study of 28 cases.骨外骨肉瘤中骨钙素和骨连接蛋白免疫反应性:28例研究
Hum Pathol. 1999 Jan;30(1):32-8. doi: 10.1016/s0046-8177(99)90297-6.
10
A review of 40 patients with extraskeletal osteosarcoma.对40例骨外骨肉瘤患者的回顾。
Cancer. 1995 Dec 1;76(11):2253-9. doi: 10.1002/1097-0142(19951201)76:11<2253::aid-cncr2820761112>3.0.co;2-8.

腹前壁骨外骨肉瘤,发生于主动脉旁放疗40年后。

Anterior abdominal wall extraosseous osteosarcoma, occurring 40 years after para-aortic irradiation.

作者信息

Furrukh Muhammad, Qureshi Asim, Mamoon Nadira, Fatima Menahil

机构信息

Radiation Oncology, Shifa Internal Hospital, Islamabad, Pakistan.

Pathology, Shifa International Hospital, Islamabad, Pakistan.

出版信息

BMJ Case Rep. 2017 Jun 22;2017:bcr-2017-219722. doi: 10.1136/bcr-2017-219722.

DOI:10.1136/bcr-2017-219722
PMID:28645924
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5534864/
Abstract

Extraskeletal osteosarcomas (OSs) are highly malignant soft tissue tumours associated with a poor prognosis. Only a few records of these rare aggressive neoplasms have been reported in the literature.We describe the case of a 49-year-old man, who presented to our tertiary care centre with a painful isolated lump around the umbilicus. After surgical biopsy, imaging and subsequent pathological analysis, the swelling was diagnosed to be a localised extraskeletal OS. He received previous radiation as treatment for testicular seminoma 40 years ago, which has been in remission ever since. He also happens to have testicular hydrocele since 10 years. He was subjected to resection and free flap reconstruction complicated by lower anterior abdominal wall haematoma and large pseudoaneurysm of the left femoral artery. Patient completed 60 Gy of adjuvant electron beam irradiation for close margins and is scheduled for adjuvant chemotherapy. We describe a brief account of his illness.

摘要

骨外骨肉瘤(OS)是一种高度恶性的软组织肿瘤,预后较差。文献中仅报道了少数关于这些罕见侵袭性肿瘤的记录。我们描述了一名49岁男性的病例,他因脐周出现疼痛性孤立肿块前来我们的三级护理中心就诊。经过手术活检、影像学检查及后续病理分析,该肿胀被诊断为局限性骨外骨肉瘤。他40年前曾接受放疗以治疗睾丸精原细胞瘤,此后一直处于缓解期。他还患有睾丸鞘膜积液10年。他接受了切除及游离皮瓣重建手术,术后出现下腹部前壁血肿和左股动脉大假性动脉瘤等并发症。患者因切缘阳性完成了60 Gy的辅助电子束照射,并计划接受辅助化疗。我们简要描述了他的病情。