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Maffucci综合征一例报告 被引量:2

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摘要 目的探讨Maffucci综合征的临床、病理及影像特点。方法对1例Maffucci综合征的临床资料、病理学、影像学表现进行回顾性分析。结果本例为17岁女性,因发现右手及右足出现多个肿物就诊。既往曾因右手多发内生软骨瘤行手术治疗。专科检查见右手及右足散在分布数十个大小不等肿物,有紫红色素沉着,压之不褪色。摄X线骨片示右手示指、中指、无名指及第二掌骨均可见骨干膨大,有不规则透亮区,骨皮质变薄,有硬化边缘及沙粒样钙化;MRI示右手及右足软组织见多个类圆形长T1长T2信号影,边界清楚。行手术治疗,术后病理报告:海绵状血管瘤(Maffucci综合征)。随访半年未见复发。结论 Maffucci综合征为多发内生软骨瘤合并血管瘤,诊断需要临床、影像和病理学三者相结合。
作者 张书田
出处 《临床误诊误治》 2012年第12期20-21,共2页 Clinical Misdiagnosis & Mistherapy
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参考文献11

  • 1Lewis R J, Ketcham A S. Maffucci syndrome: functional and neoplastic significance. Case report and review of the lit- erature[J]. J Bone Joint Surg Am, 1973,55(7) :1465-1479.
  • 2Flemming D J, Murphey M D. Enchondroma and chondrosarco- ma [ J ]. Semin Musculoskelet Radiol, 2000,4 ( 1 ) :59-71.
  • 3Sun T C, Swee R C, Shires T C, et al. Chondrosarcoma in Maffucci syndrome[JJ. J Bone Joint Surg Am, 1985,67(8) : 1214-1219.
  • 4Kaplan R P, Wang J T, Amron D M, et al. Maffuccig syn- drome: two case reports with a literature review [ J]. J Am Acad Dermatol, 1993,29(5 Pt 2) :894-899.
  • 5Schwartz H S, Zimmerman N B, Simon M A, et al. The ma- lignant potential of enchondronaatosis [ J ]. J Bone Joint Surg Am, 1987,69(2) :269-274.
  • 6Yanez S, Val-Bernal J F, Mira C, et al. Spindle cell he- mangioendotheliomas associated with multiple skeletal en- chondromas : a variant of Maffucci syndrome [ J ]. Gen Diagn Pathol, 1998,143 (5-6) :331-335.
  • 7陈曌,郭友,郑晓林,唐承富.Maffucci综合征的影像诊断(文献复习并1例报告)[J].罕少疾病杂志,2008,15(4):44-47. 被引量:8
  • 8Ahmed S K, Lee W C, Irving R M, et al. Is Ollier disease an understaging of Maffucci "s syndrome? [ J ]. J Laryngol Otol, 1999,113(9) :861-864.
  • 9Matzaroglou C, Megas P, Panagiotopoulos E, et al. A "re- verse" Maffucci syndrome: case report and short review of the literature[J]. Hell J Nucl Med, 2005,8(2) :129-131.
  • 10杨秋佳,闫庆国,黄高昇.Maffucci综合征类似Kaposi肉瘤1例[J].第四军医大学学报,2004,25(11):1056-1056. 被引量:5

二级参考文献20

  • 1杨秋佳,闫庆国,黄高昇.Maffucci综合征类似Kaposi肉瘤1例[J].第四军医大学学报,2004,25(11):1056-1056. 被引量:5
  • 2Fletcher C D M,Unni K K,Mertens F.WHO classification of tumours,pathology and genetics of tumours of soft tissue and bone[M].Lyon:IARC Press,2002:241-2.
  • 3Fukunaga M,Suzuki K,Saegusa N,Folpe A L.Composite hemangioendothelioma:report of 5 cases including one with Maffucci syndrom[J].Am J Surg Pathol,2007(10):1567-72.
  • 4Walid M S,Troup E C.Cerebellar anaplastic astrocytoma in a teenager with Ollier Disease[J].J Neurooncol,2008,89(1):59-62.
  • 5White M S,Martin P L,McLean T W.Acute myelogenous leukemia associated with Ollier disease[J].Pediatr Blood Cancer,2008,50(3):645-6.
  • 6Couvineau A,Wouters V,Bertrand G,et al.PTHR1 mutations associated with Ollier disease result in receptor loss of function[J].Hum Mol Genet,2008,17(18):2766-75.
  • 7McDermott AL, Dutt SN, Chavda SV, et al. Maffucci's syndrome: clinical and radiological features of a rare condition[J]. J Laryngol Otol, 2001;115(10):845-847.
  • 8Anburg JC, Meis-Kindblom JM, Rosenberg AE. Multiple enchondromas associated with spindle-cell hemangioendotheliomas. An overlooked variant of Maffucci's syndrome[J]. Am J Surg Pathol, 1995;19(9):1029-1038.
  • 9Resnick D, Kyriakos M, et al. Tumors and tumor-like lesions of bone: imaging and pathology of specific lesions [M]. In: Resnick D, ed. Diagnosis of bone and joint disorders. 3rd ed. Philadelphia, Pa: Saunders, 1995; 3705 3707, 4214-4215.
  • 10Yanez S, Val-Bernal JF, et al. Spindle cell hemangioendotheliomas associated with multiple skeletal enchondromas: a variant of Maffucci' s syndrome [J]. Gen Diagn Pathol 1998; 143: 331-335.

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  • 1Lewis RJ,Ketcham AS.Maffucci's syndrome:functional and neoplastic significance-csae report and review of the literature[J].J Bone Joint Surg Am,1973,55(7):1465-1479.

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