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中华诊断学电子杂志 ›› 2017, Vol. 05 ›› Issue (03) : 192 -195. doi: 10.3877/cma.j.issn.2095-655X.2017.03.013

所属专题: 文献

临床研究

腰椎原发尤文肉瘤的诊断学特征
卜凡1, 李毅1, 王文洋1, 冯强1,()   
  1. 1. 271000 泰安市中心医院检验科
  • 收稿日期:2017-05-20 出版日期:2017-08-26
  • 通信作者: 冯强
  • 基金资助:
    山东省医药卫生科技发展计划(2016WS0600)

Diagnostic features of Ewing′'s sarcoma of lumbar spine

Fan Bu1, Yi Li1, Wenyang Wang1, Qiang Feng1,()   

  1. 1. Department of Clinical Laboratory, Central Hospital of Taian City, Taian 271000, China
  • Received:2017-05-20 Published:2017-08-26
  • Corresponding author: Qiang Feng
  • About author:
    Corresponding author: Feng Qiang, Email:
引用本文:

卜凡, 李毅, 王文洋, 冯强. 腰椎原发尤文肉瘤的诊断学特征[J/OL]. 中华诊断学电子杂志, 2017, 05(03): 192-195.

Fan Bu, Yi Li, Wenyang Wang, Qiang Feng. Diagnostic features of Ewing′'s sarcoma of lumbar spine[J/OL]. Chinese Journal of Diagnostics(Electronic Edition), 2017, 05(03): 192-195.

目的

探讨腰椎原发尤文肉瘤的临床、病理学特征和影像学表现。

方法

对1例原发于腰椎尤文肉瘤患者的实验室检查、CT、磁共振、病理检查等进行分析并复习文献。

结果

患者实验室检查结果,除神经元特异性烯醇化酶111.30 μg/L外,余皆正常;X线显示T5椎体楔形变,相邻间隙变窄,CT结果示T5椎体楔形变,局部骨质后突。磁共振结果显示多椎体破坏,并局部软组织肿块形成。免疫组化结果:S-100散在+,突触核蛋白(Syn)局灶+,增值指数67(Ki-67):10%~30%,FLI-1弱+,波形蛋白(Vim)+,CD99+,CD56+,肌酸激酶(CK)-,CD3-,CD20-,甲状腺转录因子-1(TTF-1)-,髓过氧化物酶(MPO)-,CD34-,末端脱氧核苷酸转移酶(TdT)-,嗜铬蛋白A(CgA)-,CD7-,CD38-,B细胞特异性激活蛋白(PAX-5)-,CD138-,CD79a-,CK8/18-,病理诊断为尤文肉瘤。

结论

尤文肉瘤病程短,早期即可发生广泛转移,预后差,结合临床及影像学检查,可以对该病做出诊断。

Objective

To explore the clinical, pathological and imaging features of Ewing′s sarcoma in lumbar and to improve the understanding and diagnosis rate of the disease.

Methods

Laboratory tests, computed tomography (CT), magnetic resonance imaging (MRI), pathological examination of one patient with Ewing′s sarcoma in lumbar were analyzed and the related literatures were reviewed.

Results

Expect the level of Neuron Specific Enolization Enzyme was 111.30 μg/L, the rest of the laboratory test results were normal.The X-ray demonstrated T5 vertebral wedge deformation and adjacent gap narrowed.CT results showed T5 vertebral wedge deformation and local bone kyphosis.MRI results revealed multiple vertebral destruction, and local soft tissue mass formation.Immunohistochemical results: S-100, synuclein(Syn), proliferation index (Ki-67), FLI-1 were partial positive, vimentin(Vim), CD99, CD56 were positive, creatine kinase (CK), CD3, CD20, thyroid transcription factor-1(TTF-1), myeloperoxidase(MPO), CD34, terminal deoxynucleotidyl transferase(TdT), chromogranin A (CgA), CD7, CD38, B-cell specific activator protein(PAX-5), CD138, CD79a, CK8/18 were negative.Finally, pathological diagnosis of Ewing′s sarcoma were made.

Conclusions

Ewing′s sarcoma is characterized by short duration, early widespread metastases and poor prognosis.The disease can be diagnosed by clinical and imageological examination.

图1 腰椎原发尤文肉瘤患者胸部正侧位扫描图。a、b图示心肺膈未见明显异常,T5椎体楔形变,相邻间隙变窄(箭头所示)
图2 腰椎原发尤文肉瘤患者CT平扫及骨三维成像结果图。a、b 图示CT平扫示T5椎体压缩性骨折;c、d图示CT骨三维重建(箭头所示)
图3 腰椎原发尤文肉瘤患者MRI检查结果图。a,b,c 图示MR TIWI、T2WI、PDWI示T5椎体压缩性骨折;d图示MR椎体横断面平扫示骨折组织渗出(箭头所示)
[1]
Surdez D,Benetkiewicz M,Perrin V, et al.Targeting the EWSR1-FLI1 oncogene-induced protein kinase PKC-beta abolishes ewing sarcoma growth[J]. Cancer Res, 2012, 72(17): 4494-4503.
[2]
Staege M S,Hutter C,Neumann I, et al. DNA microarrays reveal relationship of Ewing family tumors to both endothelial and fetal neural crest-derived cells and define novel targets[J]. Cancer Res, 2004, 64(22): 8213-8221.
[3]
Novik VI,Krasil′nikova LA,Kolygin BA, et al. [Cytological diagnosis and prognosis in Ewing's sarcoma in children][J]. Arkh Patol, 2005, 67(2): 22-25.
[4]
Borinstein SC,Beeler N,Block JJ, et al. A Decade in Banking Ewing Sarcoma: A Report from the Children's Oncology Group[J]. Front Oncol, 2013, 3: 57.
[5]
von Eisenhart-Rothe R,Toepfer A,Salzmann M, et al.[Primary malignant bone tumors][J]. Orthopade, 2011, 40(12): 1121-1142.
[6]
Worch J,Matthay KK,Neuhaus J, et al.Ethnic and racial differences in patients with Ewing sarcoma[J]. Cancer, 2010, 116(4): 983-988.
[7]
Burningham Z,Hashibe M,Spector L, et al.The epidemiology of sarcoma[J]. Clin Sarcoma Res, 2012, 2(1): 14.
[8]
张锐,李绍林,张晓东, 等. 原发脊柱尤文肉瘤/原始神经外胚层肿瘤临床病理学特征与影像学分析[J]. 中华医学杂志, 2014, 94(23): 1808-1811.
[9]
李俊萍,边美玲,董爱华. 胃原发胚胎性横纹肌肉瘤临床诊断学特征及文献复习[J/CD]. 中华诊断学电子杂志, 2016, 4(4): 245-248.
[10]
Folpe AL,Goldblum JR,Rubin BP, et al.Morphologic and immunophenotypic diversity in Ewing family tumors: a study of 66 genetically confirmed cases[J]. Am J Surg Pathol, 2005, 29(8): 1025-1033.
[11]
Lezcano C,Clarke MR,Zhang L, et al.Adamantinoma-like Ewing sarcoma mimicking basal cell adenocarcinoma of the parotid gland: a case report and review of the literature[J]. Head Neck Pathol, 2015, 9(2): 280-285.
[12]
Kikuchi Y,Kishimoto T,Ota S, et al.Adamantinoma-like Ewing family tumor of soft tissue associated with the vagus nerve: a case report and review of the literature[J]. Am J Surg Pathol, 2013, 37(5): 772-779.
[13]
Weinreb I,Goldstein D,Perez-Ordoñez B. Primary extraskeletal Ewing family tumor with complex epithelial differentiation: a unique case arising in the lateral neck presenting with Horner syndrome[J]. Am J Surg Pathol, 2008, 32(11): 1742-1748.
[14]
Alexiev BA,Tumer Y,Bishop JA. Sinonasal adamantinoma-like Ewing sarcoma: A case report[J]. Pathol Res Pract, 2017, 213(4): 422-426.
[15]
Sumegi J,Nishio J,Nelson M, et al.A novel t(4;22)(q31;q12) produces an EWSR1-SMARCA5 fusion in extraskeletal Ewing sarcoma/primitive neuroectodermal tumor[J]. Mod Pathol, 2011, 24(3): 333-342.
[16]
Jing Z,WenYi L,JianLi L, et al.The imaging features of meningeal Ewing sarcoma/peripheral primitive neuroectodermal tumours (pPNETs)[J]. Br J Radiol, 2014, 87(1041): 20130631.
[17]
Kuleta-Bosak E,Kluczewska E,Machnik-Broncel J, et al.Suitability of imaging methods (X-ray, CT, MRI) in the diagnostics of Ewing's sarcoma in children - analysis of own material[J]. Pol J Radiol, 2010, 75(1): 18-28.
[18]
Tonyali S,Yazici S,Yesilirmak A, et al.The Ewing's sarcoma family of tumors of urinary bladder:a case report and review of the literature[J]. Balkan Med J, 2016, 33(4): 462-466.
[19]
Yu H,Ge Y,Guo L, et al.Potential approaches to the treatment of Ewing's sarcoma[J]. Oncotarget, 2017, 8(3): 5523-5539.
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