Primitive neuroectodermal tumor (PNET) is a member of the Ewing's sarcoma family of tumors (ESFT). We report a case of PNET in a 66-year-old male who presented with a large solid tumor within the parenchyma of the middle pole of the left kidney with metastases to the left adrenal gland and right ischium. A fine-needle biopsy was performed and showed a small round cell tumor. Results of immunohi...

A 13-year-old boy presented with a primitive neuroectodermal tumor (PNET) with unusual extracranial extension. Precontrast computed tomography showed the tumor as a ring-shaped high-density area which was enhanced postcontrast, with a low-density center. Magnetic resonance imaging showed the tumor as a low-intensity area on the T1-weighted images with marked enhancement by gadolinium-diethylene...

Neuroendocrine tumors (NETs) describe a heterogeneous group of tumors with a wide range of morphologic, functional, and behavioral characteristics. These tumors are generally slow growing and behave in an indolent fashion. However, they have the potential to spread, primarily to the liver and when they do, they can be life threatening and difficult to treat with current modalities. A subset of ...

Primitive neuroectodermal tumor (PNET) arise from Kulchitsky cells and are rarely seen in the female genital tract. Differential diagnosis of PNET can be made based on immunohistochemical profiles and genetic analyses. Genital tract pNETs are very aggressive pathologies with different clinical and molecular manifestations and there are no standard guidelines for treatment. We aimed to present t...

Objective To investigate the clinicopathological feature, immunological phenotype, therapy and prognosis of primary renal primitive neuroectodermal tumor (primitive neuroectodermal tumor, PNET). Method To report diagnose and treat condition of a child with renal PNET and review relevant literature. Result The male patient aged 13 years old. Color-ultrasound found 3.5 cm × 3.0cm mass of left kid...

Ewing/PNET (peripheral neuroepithelioma) tumors are rare aggressive bone sarcomas occurring in young people. Rare-disease clinical trials can require global collaborations and many years. In vivo models that as accurately as possible reflect the clinical disease are helpful in selecting therapeutics with the most promise of positive clinical impact. Human Ewing/PNET sarcoma cell lines developed...

1. department of pathology, burdwan medical college, burdwan, west bengal, india 2. department of pathology, bankura sammilani medical college, bankura, west bengal, india                   corresponding author: nirmalya chakrabarti, md; tel: (+91) 9477882332 email: [email protected] received: 06 july 2014 accepted: 03 feb. 2015 iran j cancer prev. 2015; 2:129-33.     abstract among...