Primary Orbital Myxoid Liposarcoma: A Case Report and Review of Literature

Authors

  • Chen Niu Department of Radiology, The First Affiliated Hospital of Xi’an, Jiaotong University
  • Netra Rana Department of Radiology, The First Affiliated Hospital of Xi’an, Jiaotong University
  • Zhi Gang Min Department of Radiology, The First Affiliated Hospital of Xi’an, Jiaotong University
  • Ming Zhang Department of Radiology, The First Affiliated Hospital of Xi’an, Jiaotong University

DOI:

https://doi.org/10.3126/ajms.v4i4.8311

Keywords:

orbital myxoid liposarcoma, radiotherapy, computed tomography, magnetic resonance imaging

Abstract

Liposarcomas are common malignant soft-tissue tumors, which come from primitive mesenchymal cells and differentiate into adipose tissue. These tumors are more commonly found in lower limbs and retroperitoneal region but also reported in pharynx, lung, liver, digestive tract, diaphragm, as well as in the spermatic cord. We reported a case of primary orbital myxoid liposarcoma in a 20-year-old female patient presented with a painless proptosis of the right eye. The mass was pathologically diagnosed as a myxoid liposarcoma. The tumor recurred in 9 months after surgical intervention. The second surgery was performed and followed by postoperative local radiotherapy. No recurrence has been reported after one year of follow-up. We highlighted the role of CT and MRI findings in the tumor diagnosis and the importance of local radiotherapy after surgery.

Asian Journal of Medical Science, Volume-4 (2013), Pages 28-32

DOI: http://dx.doi.org/10.3126/ajms.v4i4.8311

 

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Published

2013-08-11

How to Cite

Niu, C., Rana, N., Min, Z. G., & Zhang, M. (2013). Primary Orbital Myxoid Liposarcoma: A Case Report and Review of Literature. Asian Journal of Medical Sciences, 4(4), 28–32. https://doi.org/10.3126/ajms.v4i4.8311

Issue

Section

Case Report and Review of Literature