Results 161 to 170 of about 14,338 (204)

Sinonasal teratocarcinosarcoma: a case report of a 41-year-old female. [PDF]

Am J Transl Res
Liu M, Yang W, Zhang A, Geng H, Li G, Shi S.   +5 more
europepmc   +1 more source

[Primitive neuroectodermal tumor].

Polish journal of pathology : official journal of the Polish Society of Pathologists, 2002
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Long-Term Survival after Surgical Resection and Radiotherapy for Anterior Mediastinal Neuroblastoma in an Older Patient: A Case Report. [PDF]

Surg Case Rep
Hirai A, Kanekatsu K, Kato T.
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Primary Ewing sarcoma of the uterine cervix: a case report and comprehensive review. [PDF]

Korean J Clin Oncol
Halder S, Singhal S, Mathur S, Bakhshi S, Pandey R, Kulshrestha V, Dhamija E, Malhotra N.   +7 more
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Updates in the Management of Malignant Ovarian Germ Cell Tumors. [PDF]

O G Open
Yang J, Peng P, Xiang Y, Yang J.
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Primitive neuroectodermal tumors

Critical Reviews in Neurosurgery, 1998
The primitive neuroectodermal tumors (PNETs) of Hart and Earle constitute an important fraction of pediatric brain tumors that are clinically characterized by their aggressive behavior. In 1983, Rorke expanded the term "PNET" to include all small cell embryonal neoplasms of neuroectodermal origin, regardless of the location of the tumor. More recently,
, Nishio, , Morioka, , Fukui
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Multiple primitive neuroectodermal tumors

Journal of the American Academy of Dermatology, 1994
Primitive neuroectodermal tumors are rare, highly aggressive neoplasms that affect both sexes and occur in all age groups. They are a large group of neoplasms with neuroepithelial differentiation, including cutaneous neuroblastomas. Histopathologically they are characterized by a rather uniform population of small, dark cells, with or without Homer ...
O P, Sangüeza, P, Sangüeza, L R, Valda, C K, Meshul, L, Requena   +4 more
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