Zobrazeno 1 - 10
of 325
pro vyhledávání: '"ependymoblastoma"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 15, Iss 11, Pp 24-27 (2021)
Introduction: Small blue round cell tumours are heterogeneous group of neoplasms characterised by small, round and relatively undifferentiated cells. These tumours pose a great challenge to the histopathologist for definite diagnosis and Immunohi
Externí odkaz:
https://doaj.org/article/5fc10a68cadc45f89819cace25f953cc
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Ependymoblastoma is a rare embryonal neoplasm of the nervous system, and the entity is even rare with distant metastasis. This case can help refine the existing literature and provide lessons for the management of other patients with ependymoblastoma
Externí odkaz:
https://doaj.org/article/360829b26ed44fe99019358592244307
Autor:
Cleciton Braga Tavares, Francisca das Chagas Sheyla Almeida Gomes-Braga, Emerson Brandão Sousa, Camilla Aniele Areia Ferreira, José Nazareno Pearce de Oliveira Brito
Publikováno v:
Brazilian Neurosurgery, Vol 36, Iss 04, Pp 247-250 (2017)
The embryonal tumor with abundant neuropil and true rosettes (ETANTR) is an extremely rare variant of the primitive neuroectodermal tumor (PNET). About 80 cases have been reported since its first description in the literature, in 2000. The ETANTR occ
Externí odkaz:
https://doaj.org/article/e2ca07718f3d43158145aa2b535884c7
Autor:
Nguyen Minh Duc, Pham Minh Thong
Publikováno v:
Neurology International
Ependymoblastoma is an uncommon, exceedingly malignant brain neoplasm that adversely influences children’s quality of life. Ependymoblastoma represents a subtype of primitive neuroectodermal tumors, categorized as grade IV, according to the 2007 Wo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e86fcccf91c56e4afb320087e277476e
https://doi.org/10.3390/neurolint12030010
https://doi.org/10.3390/neurolint12030010
Akademický článek
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Autor:
Canan Akyüz, Susan L. McGovern, Nancy Philip, Ali Varan, Mary Frances McAleer, Sergio Jaramillo, David R. Grosshans, Anita Mahajan
Publikováno v:
Clinical and Translational Radiation Oncology
Clinical and Translational Radiation Oncology, Vol 15, Iss, Pp 31-37 (2019)
Clinical and Translational Radiation Oncology, Vol 15, Iss, Pp 31-37 (2019)
Highlights • ETMRs are rare but highly aggressive tumors occurring in young children. • The role of radiation in the treatment of ETMRs is poorly defined. • Of 18 long term (>36 months) survivors in the literature, 17 received radiation. • Of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f574b19dfaecc07ee4d9e88fbcfb130a
https://doi.org/10.1016/j.ctro.2018.11.002
https://doi.org/10.1016/j.ctro.2018.11.002
Autor:
Camilla Aniele Areia Ferreira, Emerson Brandão Sousa, Francisca das Chagas Sheyla Almeida Gomes-Braga, Cléciton Braga Tavares, José Nazareno Pearce de Oliveira Brito
Publikováno v:
Brazilian Neurosurgery, Vol 36, Iss 04, Pp 247-250 (2017)
The embryonal tumor with abundant neuropil and true rosettes (ETANTR) is an extremely rare variant of the primitive neuroectodermal tumor (PNET). About 80 cases have been reported since its first description in the literature, in 2000. The ETANTR occ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7eb7c22d210ac49a5a423188212e703d
https://doi.org/10.1055/s-0037-1607358
https://doi.org/10.1055/s-0037-1607358
Autor:
Jennifer Reichbach, Jamie Shoag, Joicy B Estevez, Edward Ziga, Antonello Podda, Alyssa A Cavanaugh
Publikováno v:
Biomedical Journal of Scientific & Technical Research. 26
Medulloepitheliomas (MEPLs) are rare embryonal tumors characterized by histological features that resemble those of the neural tube, the embryonic precursor to the Central Nervous System
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a54f469824167e05698acea764a37641
https://doi.org/10.26717/bjstr.2020.26.004368
https://doi.org/10.26717/bjstr.2020.26.004368
Publikováno v:
Asian Journal of Neurosurgery
Primitive neuroectodermal tumors (PNETs) are aggressive, poorly differentiated tumors in children and young adults. However, the embryonal tumor group did not include the central nervous system (CNS) PNET title and ependymoblastoma subtitle in the 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e1d2f84e436f9dd59385e7fddffb97a
https://doi.org/10.4103/ajns.ajns_30_17
https://doi.org/10.4103/ajns.ajns_30_17
Autor:
Pravin Salunke, Ridhi Sood, Bishan Dass Radotra, Amita Trehan, Richa Jain, Renu Madan, Debajyoti Chatterjee, Kirti Gupta, Chirag Kamal Ahuja
Publikováno v:
Annals of Diagnostic Pathology. 53:151745
Background Embryonal tumor with multilayered rosettes (ETMR) are a heterogenous group clinically, pathologically and topographically. Due to limited cases, data regarding its molecular genetics, pathology and prognostic factors is evolving. We retros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab53a6097f1b8204b6759f4f5b2c07ea
https://doi.org/10.1016/j.anndiagpath.2021.151745
https://doi.org/10.1016/j.anndiagpath.2021.151745