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CT诊断肩背部弹力纤维瘤14例 被引量:2

CT Diagnosis of Elastofibroma Dorsi
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摘要 目的探讨肩背部弹力纤维瘤的CT表现。方法回顾性分析14例接受胸部CT检查并经手术病理证实的EFD患者,其中12例接受CT平扫,2例同时接受CT增强扫描。分析EFD的临床特点及CT表现特征。结果 14例患者均为女性,临床表现病灶位于右侧4例、左侧8例、2例累及双侧。CT共发现16个病灶,呈扁丘状或半圆形肿块,主要呈肌样密度,内见条纹状脂肪密度,增强扫描病灶未见明显强化。结论中老年女性单侧或双侧肩胛下角区无症状性扁丘状肿块,CT表现为肌样密度伴条纹状脂肪密度无明显强化者,应考虑EFD。应双侧对照,以利于发现体表不易触及的亚临床阶段的病灶。 Objective To explore the CT findings of elastofibroma dorsi(EFD) .Methods Fourteen pa-tients with EFD confirmed by pathology were collected retrospectively .All patients underwent plain chest CT , while 2 of them underwent contrast enhanced before surgery .clinicalfeatures and CT characteristics of EFD were、all analyzed .Results Fourteen patients were all female .Clinical manifestation shown that lesions were on theright side in 4 patients ,on the left in 8 patients ,and bilateral lesion were detected in 2 patients .Masses were flat mound-like or semi-circular ,mainly were muscular-like density ,and fat density were seen of masses ,pre-senting as spaced stripe .The lesion did not enhance in 2 patients .Conclusions EFD should be considered when unilateral or bilateral subscapular areas asymptomatic masses presenting as muscle-like with striated fatspaced , not enhancing were detected on CT in middle-aged women .Bilateral CT examination is necessary for detecting sub-clinical stage lesions .
出处 《内蒙古医学杂志》 2015年第2期189-190,共2页 Inner Mongolia Medical Journal
关键词 弹力纤维瘤 X线计算机 体层摄影术 elastofibroma dorsi X-ray computed tomography
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参考文献8

  • 1Battaglia M,Vanel D,Pollastri P,et al.Imaging patterns in elastofibroma dorsi[J].Eur J Radiol,2009,72(1):16-21.
  • 2Mccomb EN,Feely MG,Neff JR,et al.Cytogentic instability predominantly involving chromosome 1,is characteristic of elastofibroma[J].Cancer Genet Cytogenet,2001,126(1):68-72.
  • 3丁长伟,刘鹏,张军,王秋实,潘诗农,郭启勇.CT诊断背部弹力纤维瘤[J].中国医学影像技术,2012,28(6):1195-1198. 被引量:14
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二级参考文献12

  • 1Fibla J, Molins L, Marco V, et al. Bilateral elastofibroma dorsi. Joint Bone Spine, 2007,74(2) : 194-196.
  • 2Battaglia M, Vanel D, Pollastri P, et al. Imaging patterns in elastofibroma dorsi. Eur J Radiol, 2009,72(1) : 16-21.
  • 3Nishida A, Uetani M, Okimoto T, et al. Bilateral elastofibroma of the thighs with concomitant subseapular lesions. Skeletal Radi- ol, 2003,32(2):116-118.
  • 4Parratt MT, Donaldson JR, Flanagan AM, et al. Elastofibroma dorsi: Mmanagement, outcome and review of the literature. J Bone Joint Surg Br, 2010,92(2) :262-266.
  • 5Malghem J, Baudrez V, Lecouvet F, et al. Imaging study find- ings in elastofibroma dorsi. Joint Bone Spine, 2004, 71 (6) : 536 541.
  • 6Hayes AJ, Alexander N, Clark MA, et al. Elastofibroma: A rare soft tissue tumour with a pathognomonic anatomical location and clinical symptom. Eur J Surg Oncol, 2004,30(4):450-453.
  • 7Mccomb EN, Feely MG, Neff JR, et al. Cytogenetic instability, predominantly involving chromosome 1, is characteristic of elasto- fibroma. Cancer Genet Cytogenet, 2001,126(1):68-72.
  • 8Ahmed MA, Subramanian SK, A1-Hashmi I, et al. Bilateral elastofibroma dorsi. Sultan Qaboos Univ Med J, 2011, 11 (3): 415-416.
  • 9Antonio B, Roberto C, Di Renzo M, et al. Elastofibroma dorsi. Surg Today, 2000,30(2) :147-152.
  • 10Alouini R, Allani M, Harzallah L, et al. Elastofibroma: Ima- ging features. J Radiol, 2005,86(11) : 1712-1715.

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