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Ewings sarcoma-primitive neuroectodermal tumor (PNET)

Known as: primitive neuroectodermal tumor, peripheral, Neuroectodermal Tumor, Peripheral Primitive, Neuroectodermal Neoplasm, Peripheral Primitive 
A group of highly cellular primitive round cell neoplasms which occur extracranially in soft tissue and bone and are derived from embryonal neural… Expand
National Institutes of Health

Related topics

Related topics

42 relations
AnemiaBlood supply aspectsEWSR1 geneEWSR1-PATZ1 Fusion Protein Expression
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Narrower (3)

Askin's tumorExtraosseous Ewings sarcoma-primitive neuroepithelial tumorPeripheral Neuroblastoma

Broader (5)

Bone neoplasmsNeuroectodermal Tumor, PrimitiveNeuroectodermal TumorsPrimary malignant neoplasm
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Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2013
Highly Cited
2013
MEK162 for patients with advanced melanoma harbouring NRAS or Val600 BRAF mutations: a non-randomised, open-label phase 2 study.
BACKGROUND Patients with melanoma harbouring Val600 BRAF mutations benefit from treatment with BRAF inhibitors. However, no… Expand
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Highly Cited
2002
Highly Cited
2002
Primary Ewing's Sarcoma/Primitive Neuroectodermal Tumor of the Kidney: A Clinicopathologic and Immunohistochemical Analysis of 11 Cases
Ewing's sarcoma/primitive neuroectodermal tumor (ES/PNET) is an extraordinarily rare primary tumor in the kidney and can be… Expand
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Review
2000
Review
2000
Molecular biology of the Ewing's sarcoma/primitive neuroectodermal tumor family.
Ewing's sarcoma (ES) and primitive neuroectodermal tumor (PNET) are members of a tumor family consistently associated with… Expand
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Highly Cited
2000
Highly Cited
2000
Immunohistochemical Detection of FLI-1 Protein Expression: A Study of 132 Round Cell Tumors With Emphasis on CD99-Positive Mimics of Ewing's Sarcoma/Primitive Neuroectodermal Tumor
The histologic and immunohistochemical differentiation of Ewing's sarcoma/primitive neuroectodermal tumor (ES/PNET) from other… Expand
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Highly Cited
1999
Highly Cited
1999
Cancer incidence and survival among children and adolescents: United States SEER Program 1975-1995.
 
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Highly Cited
1999
Highly Cited
1999
Development of peripheral lymphoid organs and natural killer cells depends on the helix–loop–helix inhibitor Id2
Transcription factors with a basic helix–loop–helix (HLH) motif have been shown to be crucial for various cell differentiation… Expand
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Highly Cited
1996
Highly Cited
1996
Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood: definition of an entity.
Clinical and pathological features of 52 infants and children with atypical teratoid/rhabdoid tumor (ATT/RhT) of the central… Expand
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Highly Cited
1996
Highly Cited
1996
Insulin-like growth factor I receptor-mediated circuit in Ewing's sarcoma/peripheral neuroectodermal tumor: a possible therapeutic target.
The disappointingly low survival rate observed in Ewing's sarcoma (ES)/peripheral neuroectodermal tumor (PNET) despite the… Expand
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Highly Cited
1994
Highly Cited
1994
Abnormal development of peripheral lymphoid organs in mice deficient in lymphotoxin.
Mice rendered deficient in lymphotoxin (LT) by gene targeting in embryonic stem cells have no morphologically detectable lymph… Expand
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Review
1993
Review
1993
Primitive Neuroectodermal Tumor and Ewing's Sarcoma
  • Louis P. Dehner
  • The American journal of surgical pathology
  • 1993
    • Corpus ID: 37201238
Many of the major solid, malignant tumors of childhood have histologic similarities that reflect their dysembryonic and primitive… Expand
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