Results 31 to 40 of about 44,148 (341)

Pediatric extraspinal sacrococcygeal ependymoma (ESE): an Italian AIEOP experience of six cases and literature review [PDF]

open access: yes, 2018
Background: Primary pediatric extraspinal sacrococcygeal ependymoma (ESE) is a very rare disease, poorly described in literature, whose diagnostic, therapeutic, and follow-up approach is still controversial.
Antonelli, Manila   +6 more
core   +1 more source

An interesting case of spinal primary peripheral primitiveneuroectodermal tumor: Rarest of the rare

open access: yesJournal of Spinal Surgery, 2016
Primitive neuroectodermal tumors (PNETs) are fast-growing undifferentiated tumors that share a common cell of origin. Primitive neuroectodermal tumors constitute less than 1% of all primary spinal tumors.
T P Jeyaselva Senthilkumar   +5 more
doaj   +1 more source

Sacrococcygeal extradural ependymoma [PDF]

open access: yesCancer, 1989
A case of lumbosacral extradural myxopapillary ependymoma is reported. The clinical, embryologic, and therapeutic features of this rare lesion are presented. The unusual entity is discussed in the light of previous experience with extradural ependymoma in the lumbosacral region.
A, Lemberger   +5 more
openaire   +2 more sources

Clinical presentation, diagnostic findings and outcome of dogs with presumptive spinal-only meningoencephalomyelitis of unknown origin [PDF]

open access: yes, 2017
Objectives: To summarise clinical presentation, diagnostic findings and long-term outcome for dogs clinically diagnosed with meningoencephalomyelitis of unknown origin affecting the spinal cord alone.
Cardy   +13 more
core   +2 more sources

Haemangioma, an uncommon cause of an extradural or intradural extramedullary mass: case series with radiological pathological correlation

open access: yesInsights into Imaging, 2015
Haemangiomas of the vertebrae, usually regarded as having little or no consequence, may display aggressive features, including extension into the extradural space, and cause significant neurological symptoms and signs necessitating treatment ...
S. McEvoy   +3 more
semanticscholar   +1 more source

Transdural Spread of Glioblastoma with Endonasal Growth in a Long-Term Survivor Patient: Case Report and Literature Review. [PDF]

open access: yes, 2016
Glioblastoma (GBM) is the most aggressive primary tumor of the central nervous system (CNS) in adults. Its growth has been always described as locally invasive. This tumor rarely penetrates dura mater and invades extracranial structures.
Antonelli, Manila   +7 more
core   +1 more source

Case Report: Recurrence of an Extradural Spinal Epidermoid Cyst Following Surgical Excision in a Dog

open access: yesFrontiers in Veterinary Science, 2022
Congenital epidermoid cysts are slow-growing, mass lesions caused by the abnormal inclusion of neuroectodermal tissue within the developing central nervous system.
Dillon Devathasan   +4 more
doaj   +1 more source

Spontaneous Intracranial Extradural Hematoma in Sickle Cell Disease

open access: yesJournal of Neurological Surgery Reports, 2015
Spontaneous extradural hematoma is rare in patients with sickle cell disease. We report a clinical case of a 19-year-old young man with sickle cell anemia who presented a sickle cell crisis complicated by the development of multiple acute extradural and ...
D. N’dri Oka   +3 more
semanticscholar   +1 more source

Cervical intraspinal extradural primitive neuroectodermal tumour in an adult

open access: yesForum of Clinical Oncology, 2014
Intraspinal extradural primitive neuroectodermal tumours (PNET) represent a rare entity that almost always carry a poor prognosis. A recent literature research revealed only four cases reported in adults.
Gogou Pinelopi V   +6 more
doaj   +1 more source

Extradural hematoma: comparative radiological study between, comatous and noncomatous patients [PDF]

open access: yes, 1992
A series of 129 patients harbouring extradural hematomas was analysed considering the neurological state immediately before operation as the most consistent variable. Seventy eight patients were considered to be comatous (Group I) and 51 were noncomatous.
Braga, Fernando M.   +2 more
core   +3 more sources

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