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本文引用的文献

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Clear cell sarcoma of soft tissue: a retrospective review and analysis of 31 cases treated at Istituto Ortopedico Rizzoli.软组织透明细胞肉瘤:Istituto Ortopedico Rizzoli 治疗的 31 例回顾性分析。
Eur J Surg Oncol. 2014 May;40(5):505-510. doi: 10.1016/j.ejso.2014.01.016. Epub 2014 Feb 2.
2
Clear cell sarcoma of the jejunum: a case report.空肠透明细胞肉瘤:一例报告。
World J Surg Oncol. 2013 Jan 25;11:17. doi: 10.1186/1477-7819-11-17.
3
Identification of biomarkers to distinguish clear cell sarcoma from malignant melanoma.鉴定生物标志物以区分透明细胞肉瘤与恶性黑色素瘤。
Hum Pathol. 2012 Sep;43(9):1463-70. doi: 10.1016/j.humpath.2011.10.022. Epub 2012 Mar 9.
4
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Int J Surg Pathol. 2012 Aug;20(4):401-6. doi: 10.1177/1066896911428073. Epub 2011 Dec 28.
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Intra-abdominal clear-cell sarcoma: a report of 3 cases, including 1 case with unusual morphological features, and review of the literature.腹腔内透明细胞肉瘤:3例报告,包括1例具有不寻常形态特征的病例,并文献复习
Int J Surg Pathol. 2012 Aug;20(4):378-85. doi: 10.1177/1066896911425485. Epub 2011 Nov 13.
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Soft tissue tumors associated with EWSR1 translocation.与 EWSR1 易位相关的软组织肿瘤。
Virchows Arch. 2010 Feb;456(2):219-34. doi: 10.1007/s00428-009-0854-3.
7
Clear cell sarcoma of the stomach.胃透明细胞肉瘤
Pediatr Blood Cancer. 2009 Aug;53(2):214-6. doi: 10.1002/pbc.22014.
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Targeting insulin-like growth factor 1 receptor in sarcomas.靶向肉瘤中的胰岛素样生长因子1受体。
Curr Opin Oncol. 2008 Jul;20(4):419-27. doi: 10.1097/CCO.0b013e328302edab.
9
Gastrointestinal melanoma or clear cell sarcoma? Molecular evaluation of 7 cases previously diagnosed as malignant melanoma.胃肠道黑色素瘤还是透明细胞肉瘤?7例先前诊断为恶性黑色素瘤病例的分子评估
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Molecular-targeted therapies in the treatment of squamous cell carcinomas of the head and neck.头颈部鳞状细胞癌治疗中的分子靶向疗法
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胰腺透明细胞肉瘤:一例病例报告及文献复习

Clear cell sarcoma of the pancreas: a case report and review of literature.

作者信息

Huang Jie, Luo Rong-Kui, Du Min, Zeng Hai-Ying, Chen Ling-Li, Ji Yuan

机构信息

Department of Pathology, Zhongshan Hospital, Fudan University Shanghai 200032, China.

出版信息

Int J Clin Exp Pathol. 2015 Feb 1;8(2):2171-5. eCollection 2015.

PMID:25973121
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4396256/
Abstract

Clear cell sarcoma (CCS), is an uncommon malignant soft tissue neoplasm that displays melanocytic differentiation with a distinct molecular profile. It is very rarely localized in gastrointestinal tract. We reported the first case of a primary CCS arising in pancreas. A 36-year-old man presented with jaundice for one month. A preoperative abdominal computer tomography showed a low-density mass in the head of pancreas. Whipple procedure was performed and the tumor was resected. Pathological examination showed polygonal or fusiform cells arranged in a uniform nested to fascicular growth pattern with thin fibrous septa. Immunohistochemical studies revealed positivity for HMB-45, Melan A, S-100, MiTF and vimentin protein. Fluorescence in situ hybridization on paraffin section showed a translocation involving the EWSR1 gene region. No BRAF and NRAS mutation was detected. The patient underwent transcatheter arterial chemoembolization (TACE) six times and eventually died of diffuse liver metastasis 10 months later. This case illustrates that the pancreas is a potential site for primary clear cell sarcoma and molecular studies play an important role in making a conclusive diagnosis.

摘要

透明细胞肉瘤(CCS)是一种罕见的恶性软组织肿瘤,具有黑素细胞分化特征及独特的分子谱。它极少定位于胃肠道。我们报告了首例发生于胰腺的原发性CCS。一名36岁男性因黄疸就诊1个月。术前腹部计算机断层扫描显示胰头有一低密度肿块。行Whipple手术并切除肿瘤。病理检查显示多边形或梭形细胞呈均匀的巢状至束状生长模式,伴有薄纤维间隔。免疫组化研究显示HMB - 45、Melan A、S - 100、MiTF和波形蛋白呈阳性。石蜡切片荧光原位杂交显示涉及EWSR1基因区域的易位。未检测到BRAF和NRAS突变。该患者接受了6次经动脉化疗栓塞(TACE),最终10个月后死于弥漫性肝转移。该病例表明胰腺是原发性透明细胞肉瘤的潜在发病部位,分子研究在做出明确诊断中起重要作用。