Title of article :
Primitive Neuroectodermal Tumor of the Kidney
Author/Authors :
Jafarian، Amir Hossein نويسنده Department of Pathology, Ghaem Hospital, Mashhad University of Medical Sciences, Mashhad, Iran , , Omidi، Abbas Ali نويسنده Dept of Pathology, Mashhad University of Medical Sciences, Mashhad , , Shamsa، ALI نويسنده , , Khajeh Ahmadi، Saeedeh نويسنده ,
Issue Information :
فصلنامه با شماره پیاپی 30 سال 2013
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.
Journal title :
Iranian Journal of Pathology (IJP)
Journal title :
Iranian Journal of Pathology (IJP)