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本文引用的文献

1
Aneurysmal bone cysts of soft tissue represent true neoplasms: a report of two cases.软组织动脉瘤样骨囊肿是真正的肿瘤:两例报告。
J Bone Joint Surg Am. 2011 May 4;93(9):e45. doi: 10.2106/JBJS.J.00534.
2
Unknown partner for USP6 and unusual SS18 rearrangement detected by fluorescence in situ hybridization in a solid aneurysmal bone cyst.在实体动脉瘤样骨囊肿中通过荧光原位杂交检测到USP6的未知伙伴和不寻常的SS18重排。
Cancer Genet. 2011 Apr;204(4):195-202. doi: 10.1016/j.cancergen.2011.01.004.
3
FOXL2 mutations in Chinese families with Blepharophimosis syndrome (BPES).FOXL2 基因突变与中国人先天性上睑下垂综合征(BPES)家系相关。
Transl Res. 2011 Jan;157(1):48-52. doi: 10.1016/j.trsl.2010.08.005. Epub 2010 Sep 8.
4
TRE17/USP6 oncogene translocated in aneurysmal bone cyst induces matrix metalloproteinase production via activation of NF-kappaB.TRE17/USP6 癌基因易位型骨囊肿通过激活 NF-κB 诱导基质金属蛋白酶的产生。
Oncogene. 2010 Jun 24;29(25):3619-29. doi: 10.1038/onc.2010.116. Epub 2010 Apr 26.
5
Metastatic potential of an aneurysmal bone cyst.动脉瘤样骨囊肿的转移潜能。
Virchows Arch. 2009 Nov;455(5):455-9. doi: 10.1007/s00428-009-0845-4. Epub 2009 Oct 17.
6
Mesenteric extraskeletal osteosarcoma with telangiectatic features: a case report.具有扩张性特征的肠系膜骨外骨肉瘤:一例报告
BMC Cancer. 2007 May 15;7:82. doi: 10.1186/1471-2407-7-82.
7
Soft-tissue aneurysmal bone cyst: report of a case with t(5;17)(q33;p13).软组织动脉瘤样骨囊肿:1例伴有t(5;17)(q33;p13)的病例报告
Pediatr Dev Pathol. 2007 Jan-Feb;10(1):46-9. doi: 10.2350/06-03-0070.1.
8
Extraosseous aneurysmal bone cyst in a 12-year-old girl.一名12岁女孩的骨外型动脉瘤样骨囊肿。
Pediatr Radiol. 2005 Dec;35(12):1240-2. doi: 10.1007/s00247-005-1560-1. Epub 2005 Sep 20.
9
Aneurysmal bone cyst variant translocations upregulate USP6 transcription by promoter swapping with the ZNF9, COL1A1, TRAP150, and OMD genes.动脉瘤样骨囊肿变异易位通过与ZNF9、COL1A1、TRAP150和OMD基因启动子交换上调USP6转录。
Oncogene. 2005 May 12;24(21):3419-26. doi: 10.1038/sj.onc.1208506.
10
USP6 and CDH11 oncogenes identify the neoplastic cell in primary aneurysmal bone cysts and are absent in so-called secondary aneurysmal bone cysts.USP6和CDH11癌基因可识别原发性动脉瘤样骨囊肿中的肿瘤细胞,而在所谓的继发性动脉瘤样骨囊肿中则不存在。
Am J Pathol. 2004 Nov;165(5):1773-80. doi: 10.1016/S0002-9440(10)63432-3.

一名10岁女孩的软组织动脉瘤样骨囊肿。

Soft tissue aneurysmal bone cyst in a 10-year-old girl.

作者信息

Hao Yongqiang, Wang Lei, Yan Mengning, Jin Fangchun, Ge Shengfang, Dai Kerong

机构信息

Department of Orthopaedics Shanghai Key Laboratory of Orthopaedic Implant, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, P.R. China.

出版信息

Oncol Lett. 2012 Mar;3(3):545-548. doi: 10.3892/ol.2011.530. Epub 2011 Dec 21.

DOI:10.3892/ol.2011.530
PMID:22740948
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3362609/
Abstract

We report the case of a 10-year-old girl with a soft tissue aneurysmal bone cyst (STABC) located in the posterior aspect of the left shoulder. Conventional radiography revealed an oblong mass with a calcified rim. On the computed tomography scan, the lesion appeared to have a non-uniform intralesional density with an incomplete rim. Magnetic resonance imaging revealed a multi-cavity lesion with fluid-fluid levels. Following pathological examination, the lesion was diagnosed as a STABC. This may be only the twentieth reported case in the English literature of this extremely rare benign tumor occurring in soft tissue. Eight months after surgery the patient was assessed at our outpatient clinic and found to have excellent mobility of her left shoulder and no sign of recurrence.

摘要

我们报告了一例10岁女孩的病例,其软组织动脉瘤样骨囊肿(STABC)位于左肩后部。传统X线摄影显示一个有钙化边缘的椭圆形肿块。在计算机断层扫描上,病变显示内部密度不均匀,边缘不完整。磁共振成像显示一个有多腔且有液-液平面的病变。经过病理检查,该病变被诊断为STABC。这可能是英文文献中报道的这种极其罕见的发生于软组织的良性肿瘤的第20例。手术后八个月,患者在我们的门诊接受评估,发现左肩活动度极佳,无复发迹象。