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Information Journal Paper

Title

RETROPERITONEAL MESENCHYMAL CHONDROSARCOMA A CASE REPORT

Pages

  0-0

Keywords

1)CANCER 2) MESENCHYMAL CHONDROSARCOMA 3) CHONDROID TUMORS 4) RETROPERITONEAL TUMORSQ4

Abstract

 Mesenchymal chondrosarcoma(MC) was first described in 1959. MC is a rare tumor arising in bone or soft tissue which is composed of well differentiated cartilage with in a proliferation of primitive mesenchymal cell. MC occurs most often in the second and third decades of life. The prognosis is poor, local recurrence and metastases are frequent. A 32 year old, white female consulted a physician for abdominal pain, nausea and vomiting. Computed tomographic(CT) scan of the abdomen disclosed a huge retroperitoneal mass with large area of necrosis located at the left side. With probable diagnosis of kidney tumor, left nephrectomy and splenectomy was performed for the patient. While surgery a retroperitoneal mass occupying the left side with adhesion to the adjacent viscera was detected and removed. Histologic examination revealed mesenchymal chondrosarcoma.

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  • Cite

    APA: Copy

    SHAYANFAR, N., AMINI, E., & MIRZAMANI, N.. (2003). RETROPERITONEAL MESENCHYMAL CHONDROSARCOMA A CASE REPORT. RAZI JOURNAL OF MEDICAL SCIENCES (JOURNAL OF IRAN UNIVERSITY OF MEDICAL SCIENCES), 10(33), 0-0. SID. https://sid.ir/paper/360670/en

    Vancouver: Copy

    SHAYANFAR N., AMINI E., MIRZAMANI N.. RETROPERITONEAL MESENCHYMAL CHONDROSARCOMA A CASE REPORT. RAZI JOURNAL OF MEDICAL SCIENCES (JOURNAL OF IRAN UNIVERSITY OF MEDICAL SCIENCES)[Internet]. 2003;10(33):0-0. Available from: https://sid.ir/paper/360670/en

    IEEE: Copy

    N. SHAYANFAR, E. AMINI, and N. MIRZAMANI, “RETROPERITONEAL MESENCHYMAL CHONDROSARCOMA A CASE REPORT,” RAZI JOURNAL OF MEDICAL SCIENCES (JOURNAL OF IRAN UNIVERSITY OF MEDICAL SCIENCES), vol. 10, no. 33, pp. 0–0, 2003, [Online]. Available: https://sid.ir/paper/360670/en

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