期刊文献+

软组织恶性纤维组织细胞瘤影像诊断与鉴别诊断 被引量:4

下载PDF
导出
摘要 目的探讨经手术和病理确诊的软组织恶性纤维组织细胞瘤的CT和MRI特点。方法回顾分析山东省菏泽市立医院放射科2008~2013年经手术和病理确诊的21例软组织恶性纤维组织细胞瘤患者。CT扫描17例,MRI扫描2例,CT和MRI扫描2例。平扫16例,CT增强2例,MRI增强2例,CT和MRI均增强者1例。结果 21例软组织恶性纤维组织细胞瘤患者中发生于下肢12例,上肢5例,胸骨和胸壁2例,肾脏1例,盆腔1例。其中上下肢发病率最高,占81%。不规则分叶状17例,规则类圆形4例,其中,不规则分叶状比例最高,占81%。21例中伴囊变坏死者5例,占24%。5例增强扫描病例中,均可见早期不均匀明显强化。结论软组织恶性纤维组织细胞瘤的临床和影像学特点具有相对特征性,充分认识其特征,有助于提高术前诊断正确率。 Objective To discuss the CT and MRI features of malignant ifbrohistiosarcoma of soft tissue conifrmed by operation and pathology. Methods 21 cases from 200 to 2013 in the radiology department of our hospital were reviewed. 17 cases scanned with CT, 2 cases scanned with MRI, 2 cases scanned with CT and MRI. 16 cases scanned with CT pre-contrast, and 2 cases used CT post contrast, 2 cases used MRI post contrast, 1 case scanned with CT and MRI post contrast. Results 12 cases occurred in the lower limbs, 5 cases upper limbs, 2 cases of sternum and chest wall, 1 case kidney, 1 case pelvic. The upper and lower limbs accounting for 81%. Irregular and lobulated mass 17 cases, accounted for 81%, roundly mass 4 cases, Masses with deterioration were found in 5 patients, accounted for 24%. 5 cases of post contrast enhanced unequally and early. Conclusion The clinical and imaging of malignant ifbrohistiosarcoma of soft tissue are relatively characteristic, fully understand its characteristics, will help to improve the accuracy rate of preoperative diagnosis.
作者 刘伟娟
出处 《当代医学》 2014年第28期70-71,共2页 Contemporary Medicine
关键词 软组织 恶性纤维组织细胞瘤 影像诊断 Soft tissue Malignant fibrohistiosarcoma Imaging diagnosis
  • 相关文献

参考文献2

二级参考文献13

  • 1王敏,李勇刚,张景峰,王仁法,吴翠环,李小明,张伶,夏黎明,王承缘.骨原始神经外胚叶肿瘤影像学表现[J].临床放射学杂志,2005,24(6):531-534. 被引量:7
  • 2张碧云,陈自谦,肖慧.外周性原始神经外胚层肿瘤的CT与MRI表现[J].中国医学影像技术,2006,22(1):129-131. 被引量:22
  • 3郁万江,杜湘珂,徐爱德.骨与软组织周围性原始神经外胚层肿瘤的临床影像诊断[J].中华放射学杂志,2007,41(1):69-71. 被引量:5
  • 4Khong PL, Chan GC, Shek TW, et al. Imaging of peripheral PNET: common and uncommon locations. Clin Radiol, 2002,57 (4) :272-277.
  • 5Tsao AS, Roth LM, Sandier A, et al. Cervical primitive neuroectodermal tumor. Gynecol Oneol, 2001,83(1) : 138-142.
  • 6Ishii N, Hiraga H, Sawamura Y, et al. Alternative EWS-FLI1 fusion gene and MIC2 expression in peripheral and central primitive neuroectodermal tumors. Neuropathology, 2001,21 ( 1 ) : 40-44.
  • 7Mobley BC, Roulston D, Shah GV, et al. Peripheral primitive neuroectodermal tumour/Ewing's sarcoma of the craniospinal vault: ease reports and review. Hum Pathol, 2006, 37 (7): 845-853.
  • 8Kampman WA, Kros JM, De Jong TH, et al. Primitive neuroectodermal tumours (PNETs) located in the spinal canal; the relevance of classification as central or peripheral PNET: case report of a primary spinal PNET occurrence with a critical literature review. J Neurooncol, 2006,77(1) :65-72.
  • 9Furuno Y, Nishimura S, Kamiyama H, et al. lntracranial peripheral type primitive neuroectodermal tumor. Neurol Med Chit (Tokyo), 2008,48(2) :72-76.
  • 10Utsunomiya A, Uenohara H, Suzuki S, et al. A case of peripheral-type primitive neuroeetodermal tumor arising in the duramater at the frontal base. No To Shinkei, 2004,56(3):237 241.

共引文献29

同被引文献71

  • 1O' brien JE, Stout AP. Malignaent fibrous xanthomas [ J]. Cancer, 1964,17 : 1445 - 1455.
  • 2Romeo S, Bovee JV, Kroon HM, et al. Malignant fibrous histiocytoma and fibrosarcoma of bone: a re - assessment in the lightofcurrently employed morphological,immunohistochemical and molecular approa- ches[J]. Irchows Arch,2012,461 (5) :561 -570.
  • 3Bohn OL, de Leen EA, Lezama O, et al. Pulmonary artery sarcoma with angiosarcoma phenotype mimicking pleomorphicma lignant fi- brous histiocytoma : a casereport [ J ]. Diagn Pathol,2012,7 : 154.
  • 4Choi BH, Yoon SH, Lee S,et al. Primary malignant fibrous histiocyto- ma in mediastinum : imaging with ( 18 ) F - FDG PET/CT [ J ]. Nucl Med Mol Imaging,2012,46(4) :304 -307.
  • 5Faizi NA, Thulkar S, Sharma R, et al. Magnetic resonance imaging and positron emission tomography - computed tomography evaluation of soft tissue sarcoma with surgical and histopathological correlation [J]. Indian J Nucl Med,2012,27(4) :213 -220.
  • 6Yao D, Dai C. Clinical characteristics of the primary hepatic malig- nant fibrous histiocytoma in China : case report and review of the liter- ature[ J]. World J Surg Oneol,2012,10( 1 ) :2.
  • 7Mertens F, Romeo S, Bovee JV. Reclassification and subtyping of so - called malignant fibrous histiocytoma of bone : comparison with cy- togenetic features[ J]. Clin Sarcoma Res,2011,1 (1) :10.
  • 8Matsuo T, Shimose S, Kubo T, et al. Alternative lengthening of telo- meres as a prognostic factor in malignant fibrous histiocytomas of bone[ J]. Anticaneer Res,2010,30( 12 ) :4959 -4962.
  • 9Otsuka T, Harada A, Wakida K, et al. Resection of malignant fibrous histiocytoma through a combined thoracic and abdominal wall ap- proach[ J]. Kyobu Geka,2012,65 (5) :389 - 392.
  • 10Vasileios KA, Eward WC, Bfigman BE. Surgical treatment and prog- nosis in patients with high - grade soft tissue malignant fibrous histio- eytoma of the extremities [ J ]. Arch Orthop Trauma Surg, 2012,132 (7) :955 -961.

引证文献4

二级引证文献20

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部