Results 31 to 40 of about 187,996 (306)

Undifferentiated nasopharyngeal carcinoma with isolated central nervous system metastasis [PDF]

Archive of Oncology, 2004
Central nervous system (CNS) metastasis from nasopharyngeal carcinoma is an extremely rare event. Here, we report a case of nasopharyngeal carcinoma with isolated CNS metastases 45 months after the successful treatment of primary tumor.
Ozyar Enis, Yazici Gozde, Tezel Gaye, Cila Aysenur, Ozcan-Ekin Osman   +4 more
doaj   +1 more source

A Rare Case of Spontaneous Remission and Relapse of a Primary Central Nervous System Lymphoma

Acta Médica Portuguesa, 2018
Primary central nervous system lymphoma remission after steroid treatment is a well-known phenomenon, but remission without any type of treatment is extremely rare. We present a rare case of spontaneous remission of a diffuse large B-cell lymphoma of the
Rui Ramos, João Soares Fernandes, Marta Almeida, Rui Almeida   +3 more
doaj   +1 more source

Intracranial transplantation of the tumor induced by adenovirus type 12 in Syrian hamster--an experimental brain tumor model [PDF]

, 1971
A method of intracranial transplantation of the tumor induced by adenovirus type 12 in syrian hamster has been described. The incidence of intracranial tumor development was 86 (90.5 %) out of 95 animals and the average survival time and tumor size at ...
Tabuchi, Kazuo
core   +1 more source

Brainstem cavernous malformation

Brazilian Neurosurgery, 2013
Cavernous malformation (CM) of the central nervous system (CNS) are acquired or developmental vascular malformations that represent the 5% to 15% of all vascular malformations of the CNS.
Ariel Roberto Estramiana, Diana Lara Pinto de Santana, Eberval Gadelha Figueiredo, Manoel Jacobsen Teixeira   +3 more
doaj   +1 more source

CLINICAL, DEMOGRAPHIC, ANATOMOPATHOLOGICAL, AND MOLECULAR FINDINGS IN PATIENTS WITH MEDULLOBLASTOMA TREATED IN A SINGLE HEALTH FACILITY

Revista Paulista de Pediatria, 2020
Objective: To describe the clinical, demographic, anatomopathological, molecular, and survival characteristics of patients with medulloblastoma. Methods: Retrospective study based on patient information obtained from the review of medical records ...
Iva Loureiro Hoffmann, Izilda Aparecida Cardinalli, José Andrés Yunes, Ana Luiza Seidinger, Ricardo Mendes Pereira   +4 more
doaj   +2 more sources

Long-term survival for a cohort of adults with cerebral palsy [PDF]

, 2006
The aim of this study was to investigate long-term survival and examine causes of death in adult patients with cerebral palsy (CP). A 1940–1950 birth cohort based on paediatric case referral allows for long-term survival follow-up.
Blair, Cox, Evans, Evans, Hutton, Hutton, Hutton, Jane L Hutton, Karla Hemming, Maudsley, Peter O D Pharoah, Strauss, Strauss, Strauss, Strauss, Surveillance of Cerebral Palsy in Europe., Woods, Woods, Woods   +18 more
core   +1 more source

Cerebellar large B-cell lymphoma: a case report

Journal of Medical Case Reports, 2018
Background Primary central nervous system lymphoma is a rare, malignant non-Hodgkin lymphoma that can arise in the brain, spinal cord, eye, leptomeninges, or cranial nerves.
Malik Ghannam, Shaden Mansour, Fareed Jumah, Brent Berry, Albertine Beard   +4 more
doaj   +1 more source

Central nervous system manifestations as initial presentation of plasma cell disorders: Differential management of 3 cases based on disease extent

Current Problems in Cancer: Case Reports, 2023
Central nervous system (CNS) manifestations of plasma cell neoplasms are exceedingly uncommon. CNS multiple myeloma (MM) carries a dismal prognosis, and limited evidence exists to guide management of these patients.
Kyle McGrath, Graeme A. Fenton, Robert P. Seifert, Keith R. Peters, John W. Hiemenz, Erin A. Dean   +5 more
doaj   +1 more source

Tumors in von Hippel–Lindau Syndrome: From Head to Toe—Comprehensive State-of-the-Art Review [PDF]

, 2018
Von Hippel–Lindau syndrome (VHL) is an autosomal-dominant hereditary tumor disease that arises owing to germline mutations in the VHL gene, located on the short arm of chromosome 3.
Bhalla, Sanjeev, Ganeshan, Dhakshinamoorthy, Lubner, Meghan G., Menias, Christine O., Pickhardt, Perry J., Ramalingam, Preetha, Sandrasegaran, Kumaresan   +6 more
core   +1 more source

Neurofibromatosis 2

Medical Journal of Dr. D.Y. Patil University, 2015
Neurofibromatosis 2 is a rare autosomal dominant neurocutaneous disorder classically characterized by bilateral acoustic schwannomas. Multiple other central, as well as peripheral central nervous system neoplasms as meningiomas and ependymomas, are also ...
Abhijit M Patil, Shubreet Randhawa, Abhimanyu B Kelkar, Rushikesh A Naik   +3 more
doaj   +1 more source