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Information Journal Paper

Title

PRIMITIVE NEUROECTODERMAL TUMOR OF THE KIDNEY (CASE REPORT)

Pages

  123-126

Abstract

PRIMITIVE NEUROECTODERMAL TUMOR (PNET) is an uncommon malignancy of bone and soft tissue witch rarely occurs in the KIDNEY. In more than 90% of the cases, the tumor cells relieves a balanced translocation (11, 22) (q24, q12). Immunohistochemical staining may be required for diagnosis of PNET. The cells of tumor express CD99, vimentin, NSE, FL1 but do not express Ck, LCA, myogenin, and WT1. We present a 36-year –old female with left-side tender abdominal swelling, and history of trauma to abdominal. CT imaging confirmed a huge solid mass of KIDNEY, also extending into renal pelvis. Histological section of the lesion showed a malignant proliferation of small round cells in rosette-like pattern with foci of necrosis area. Tumor cells expressed high level of CD 99 antigen. The diagnosis of the lesion was PRIMITIVE NEUROECTODERMAL TUMORs (PNET). Following-up after 6 months showed no recurrence.

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  • Cite

    APA: Copy

    JAFARIAN, AMIR HOSSEIN, OMIDI, ABBAS ALI, SHAMSA, ALI, & KHAJEH AHMADI, SAEEDEH. (2013). PRIMITIVE NEUROECTODERMAL TUMOR OF THE KIDNEY (CASE REPORT). IRANIAN JOURNAL OF PATHOLOGY (IJP), 8(2), 123-126. SID. https://sid.ir/paper/595999/en

    Vancouver: Copy

    JAFARIAN AMIR HOSSEIN, OMIDI ABBAS ALI, SHAMSA ALI, KHAJEH AHMADI SAEEDEH. PRIMITIVE NEUROECTODERMAL TUMOR OF THE KIDNEY (CASE REPORT). IRANIAN JOURNAL OF PATHOLOGY (IJP)[Internet]. 2013;8(2):123-126. Available from: https://sid.ir/paper/595999/en

    IEEE: Copy

    AMIR HOSSEIN JAFARIAN, ABBAS ALI OMIDI, ALI SHAMSA, and SAEEDEH KHAJEH AHMADI, “PRIMITIVE NEUROECTODERMAL TUMOR OF THE KIDNEY (CASE REPORT),” IRANIAN JOURNAL OF PATHOLOGY (IJP), vol. 8, no. 2, pp. 123–126, 2013, [Online]. Available: https://sid.ir/paper/595999/en

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