Results 141 to 150 of about 12,013 (184)
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Primitive Neuroectodermal Tumor (Peripheral Neuroblastoma)

Ultrastructural Pathology, 1985
(1985). Primitive Neuroectodermal Tumor (Peripheral Neuroblastoma) Ultrastructural Pathology: Vol. 9, No. 1-2, pp. 59-64.
J M, Nesland   +3 more
openaire   +2 more sources

Peripheral Primitive Neuroectodermal Tumor - PNET

Acta chirurgiae orthopaedicae et traumatologiae Cechoslovaca, 2006
The authors describe three cases of peripheral primitive neuroectodermal tumor. The tumor was found in soft tissues of the crus, shoulder girdle and perineum, and was also located paravertebrally and epidurally at the level of L1-L2 vertebrae. Radiological findings were not specific for this disease. The results of imaging methods (sonography, CT, MRI,
J, Koudelová   +5 more
openaire   +2 more sources

A case report of neonatal orbital peripheral primitive neuroectodermal tumor and literature review

European Journal of Ophthalmology, 2020
Primitive neuroectodermal tumors are rare malignant neoplasms from primitive neural crest cells. Most primitive neuroectodermal tumors occur in the central and sympathetic nervous systems.
Yian Li   +6 more
semanticscholar   +1 more source

Malignant peripheral primitive neuroectodermal tumor of the kidney

Cancer Genetics and Cytogenetics, 2002
Ewing family of tumors is a group of highly aggressive neoplasias that occur most commonly in the first two decades of life. These tumors are most frequently localized in bones, less frequently in soft tissues. They usually appear as undifferentiated small round-cell tumors. With current treatment regiments, 5-year disease-free survival rates exceed 60%
Ales, Vicha   +8 more
openaire   +2 more sources

Primary Peripheral Primitive Neuroectodermal Tumor of the Prostate on 18F-DCFPyL PET/CT.

Clinical Nuclear Medicine, 2020
Peripheral primitive neuroectodermal tumor (PNET) is a group of malignant tumors composed of small round cells. Peripheral PNET usually originates in the skeletal system. However, the presence of PNET lesion in prostate is extremely rare.
Yachao Liu, Baixuan Xu
semanticscholar   +1 more source

Mouth metastasis of peripheral primitive neuroectodermal tumor

Oral Diseases, 2005
We describe a case of oral metastasis of peripheral primitive neuroectodermal tumor (pPNET) in a 68‐year‐old man, who presented the primary lesion in the chest. Oral metastasis of pPNETs is very rare and we have not found any similar case reported in the English literature.
C M, Pereira   +4 more
openaire   +2 more sources

Ovarian Primitive Neuroectodermal Tumor: Are You Central or Peripheral?

International Journal of Gynecological Pathology, 2021
Primitive neuroectodermal tumors (PNETs) of the ovary are rare, highly aggressive neoplasms with fewer than 100 cases described. PNETs of the ovary can be classified as either peripheral or central types.
S. Bachert   +3 more
semanticscholar   +1 more source

A case of peripheral primitive neuroectodermal tumor of the ovary

International Journal of Gynecological Cancer, 2004
Peripheral primitive neuroectodermal tumor (PNET) belongs to the PNET/Ewing's sarcoma family. PNET is a small round cell tumor of putative neuroectoderm origin and is the second most common sarcoma among children and young adults. It may occur anywhere in the body and within any age group; however, it is most likely to occur in the bone and soft ...
K-J, Kim   +4 more
openaire   +2 more sources

Primary vulvar Ewing sarcoma/peripheral primitive neuroectodermal tumor with pelvic lymph nodes metastasis: A case report and review of literature

The journal of obstetrics and gynaecology research, 2020
Ewing sarcoma (ES) and peripheral primitive neuroectodermal tumors (pPNET) are soft tissue tumors that generally affect the bones. Extraosseous ES/pPNET has been rarely reported.
A. El Housheimi   +8 more
semanticscholar   +1 more source

Peripheral Primitive Neuroectodermal Tumor After Radiotherapy

Clinical Orthopaedics & Related Research, 2003
A 41-year-old man had a peripheral neuroectodermal tumor develop at the distal third of the fibula 4 years after radiotherapy for relapsed villonodular synovitis. This type of sarcoma usually is classified into the heterogeneic group of small round-cell bone tumors as a subdivision of Ewing's sarcomas.
Juan L, Cebrián   +5 more
openaire   +2 more sources

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