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弥漫性脂肪纤维瘤病1例诊治 被引量:3

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摘要 脂肪纤维瘤病是一种罕见的软组织交界性肿瘤,术后易复发,但不转移,因少见易造成误诊。本病国内外报道较少,其临床表现为无痛性、生长缓慢肿块[1-2]。本文报告1例颈背部弥漫性脂肪纤维瘤病患者的诊治。1病例资料患者女,47岁,2005年因颈、背部肿物(约10 cm×10 cm)就诊于当地医院,考虑为脂肪瘤,遂行手术切除。2008年患者颈背部肿物复发,就诊于我院。超声及CT检查提示:颈、背部脂肪样组织堆积。
出处 《解放军医学院学报》 CAS 2013年第8期868-868,872,共2页 Academic Journal of Chinese PLA Medical School
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参考文献8

  • 1哈英娣,任芳,高自芳.脂肪纤维瘤病的临床病理特点[J].罕少疾病杂志,2009,16(4):6-8. 被引量:7
  • 2崔金平,肖斌.1例脂肪纤维瘤病的诊治[J].军医进修学院学报,2011,32(1):88-89. 被引量:5
  • 3Fetsch JF,Miettinen M,Laskin WB. A clinicopathologic study of 45 pediatric soft tissue tumors with an admixture of adipose tissue and fibroblastic elements,and a proposal for classification as lipofibromatosis[J].{H}American Journal of Surgical Pathology,2000,(11):1491-1500. 被引量:1
  • 4Ayadi L,Charfi S,Ben Hamed Y. Pigmented lipofibromatosis in unusual location:case report and review of the literature[J].{H}VIRCHOWS ARCHIV-AN INTERNATIONAL Journal OF PATHOLOGY,2008,(04):465-467. 被引量:1
  • 5Nuruddin M,Osmani M,Mudhar HS. Orbital lipofibromatosis in a child:a case report[J].Orbit,2010,(06):360-362. 被引量:1
  • 6Deepti AN,Madhuri V,Walter NM. Lipofibromatosis:report of a rare paediatric soft tissue tumour[J].{H}Skeletal Radiology,2008,(06):555-558. 被引量:1
  • 7Greene AK,Karnes J,Padua HM. Diffuse lipofibromatosis of the lower extremity masquerading as a vascular anomaly[J].{H}Annals of Plastic Surgery,2009,(06):703-706. 被引量:1
  • 8Walton JR,Green BA,Donaldson MM. Imaging characteristics of lipofibromatosis presenting as a shoulder mass in a 16-month-old girl[J].{H}Pediatric Radiology,2010,(Suppl 1):S43-S46. 被引量:1

二级参考文献17

  • 1唐浩,刘义成,涂茜,刘海滨,梅海清,舒章华.颅内脂肪瘤伴脑挫伤1例[J].罕少疾病杂志,2007,14(2):38-39. 被引量:1
  • 2王坚,朱雄增.软组织肿瘤病理学.北京:人民卫生出版社,2008:490. 被引量:43
  • 3A. N. Deeptil, Vrisha gadhuri , Noel Malcolm Walterl2 and Rekha Aley Cherian3, Lipofibromatosis: report of a rare paediatric soft tissue tumour, Skeletal Radiology, 2008, (37),6:555-558. 被引量:1
  • 4B. Herrmann, L. Dehner, J. Forsen, Jr. Lipofibromatosis presenting as a pediatric neck mass, International Journalof Pediatric Otorhinolaryngology, Volume 68, Issue 11, Pages 1545-1549. 被引量:1
  • 5J.F. Fetsch, M Miettinen, W.B. Laskin, M. Michal, F.M. Enzinger, h clinicopathotogic study of 45 pediatric soft tissue tumors with an admixture of adipose tissue and fibroblastic elements, and a proposal for classification as lipofibromatosis, Am. J. Surg. Pathol. 24(2000)1491- 1500. 被引量:1
  • 6Fetsch JF, Miettinen M, Laskin WB, et al. A clinicopathologic study of 45 pediatric soft tissue tumors with an admixture of adipose tissue and fibroblastic elements, and a proposal for classification as lipofibromatosis [J ] . Am J Surg Pathol, 2000, 24 ( 11 ) : 1491- 1500. 被引量:1
  • 7孙保存.软组织与骨肿瘤病理学与遗传学(世界卫生组织肿瘤分类及诊断标准系列)[M].1版.北京:人民卫生出版社,2006:65-66. 被引量:1
  • 8Deepti AN, Madhuri V, Walter NM, et al. Lipofibromatosis : report of a rare paediatric soft tissue tumour [ J ] . Skeletal Radiol, 2008, 37 (6) : 555-558. 被引量:1
  • 9KenneyB, Richkind KE, Friedlaender G, et al. Chromosomal rearrangements in lipofibromatosis [ J ] . Cancer Genet Cytogenet, 2007, 179 (2): 136-139. 被引量:1
  • 10Ayadi L, Charfi S, Ben Hamed Y, et al. Pigmented lipofibromatosis in unusual location : case report and review of the literature [ J ] . Virchows Arch, 2008, 452 ( 1 ) : 115-117. 被引量:1

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