نتایج جستجو برای: neuroectodermal tumor ppnet

تعداد نتایج: 430336  

Journal: :Arkhiv patologii 2001
A P Kuczynski E S Gugelmin R A Netto

OBJECTIVES: To characterize primitive neuroectodermal tumor of the kidney as a differential diagnosis for Wilms tumor, and to emphasize the severity of the disease. METHODS: We report the case of a patient with a diagnosis of primitive neuroectodermal tumor of the kidney who underwent nephrectomy and complete tumor resection combined with chemotherapy. RESULTS: Initially, the response of the pa...

Journal: :Journal of Medical Sciences 2018

Journal: :Journal of Indian Association of Pediatric Surgeons 2007

Journal: :American Journal of Clinical Pathology 2022

Abstract Introduction/Objective Ewing sarcoma is a cancer involving the bones or tissue around bones. It second most common malignant bone tumour comprising 10-15% of all primary tumours, commonly affecting children and young adults. can also be seen in adults also. Males are more affected then females. Any but lower extremity, pelvis, upper axial skeleton ribs, face cases. Similar histology tu...

2015
Cheng Yang Hanjiang Xu Jun Zhou Zongyao Hao Jianzhong Wang Changmin Lin Li Zhang Xia Zhu Chaozhao Liang

Primitive neuroectodermal tumor (PNET) is a malignant small round cell tumor and typically arises from bone or soft tissue in adolescents and young adults. Renal PNET is extraordinarily rare and exhibits highly aggressive biological behavior with poor prognosis.We present here a new case of renal PNET in a 31-year-old female. The patients were referred to our hospital because of left flank pain...

2015
Monica Malik Irukulla Deepa M Joseph

Introduction: Ewing sarcoma family of tumors (ESFT) are a group of small round cell tumors showing varying degrees of neuroectodermal differentiation with Ewing sarcoma being the least differentiated. Primitive neuroectodermal tumors (PNET) show neuroectodermal differentiation by light microscopy, immune histochemistry (IHC) or electron microscopy [1]. According to WHO classification of bone an...

Journal: :Neoplasia 2005
Timothy R Gershon Orit Oppenheimer Steven S Chin William L Gerald

Neuroectodermal tumor cells, like neural crest (NC) cells, are pluripotent, proliferative, and migratory. We tested the hypothesis that genetic programs essential to NC development are activated in neuroectodermal tumors. We examined the expression of transcription factors PAX3, PAX7, AP-2alpha, and SOX10 in human embryos and neuroectodermal tumors: neurofibroma, schwannoma, neuroblastoma, mali...

Journal: :iranian journal of radiology 0
davood sharifi doloui department of gastroenterology and liver disease, ghaem hospital, mashhad university of medical sciences, mashhad, iran tahereh fakharian department of gastroenterology and liver disease, ghaem hospital, mashhad university of medical sciences, mashhad, iran; department of gastroenterology and liver disease, ghaem hospital, mashhad university of medical sciences, mashhad, iran. tel:+98-5113645225, fax: +98-5118409612 vahid yahyavi department of gastroenterology and liver disease, ghaem hospital, mashhad university of medical sciences, mashhad, iran sirous nekooei department of radiology, ghaem hospital, mashhad university of medical sciences, mashhad, iran hamid reza zivarifar department of gastroenterology and liver disease, ghaem hospital, mashhad university of medical sciences, mashhad, iran kamran ghafarzadegan department of pathology, razavi hospital, mashhad, iran

primitive neuroectodermal tumor (pnet) is usually an aggressive, rapidly progressing and metastasizing tumor. occurrence of this type of tumor in the kidney is considered as unusual and few cases have been reported so far. we present a metastatic pnet arising probably from the kidney in a 17-year-old female patient with local invasion and metastasis to the stomach. pnet should be considered as ...

Journal: :Cancer research 1990
C Raffel F E Gilles K I Weinberg

The loss of genetic material from specific chromosomal locations has been identified for a number of pediatric tumors. This loss has been taken as evidence for the importance of tumor suppressor genes at these loci in the genesis of these tumors. One of these pediatric tumors, the primitive neuroectodermal tumor of the central nervous system, has not been well studied. In this report, an analys...

2011
Farah Farzaneh Hamidreza Rezvani Parisa Taherzadeh Boroujeni Farzaneh Rahimi

INTRODUCTION Peripheral primitive neuroectodermal tumor of the cervix uteri is extremely rare. Between 1987 and 2010, there were only nine cases reported in the English literature, with considerably different management policies. CASE PRESENTATION A 45-year-old Iranian woman presented to our facility with a primitive neuroectodermal tumor of the cervix uteri. Her clinical stage IB2 tumor was ...

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