Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

41 results
Display

The Continuing Value of Ultrastructural Observation in Central Nervous System Neoplasms in Children

Kim NR, Park SH

Central nervous system (CNS) neoplasms are the second most common childhood malignancy after leukemia and the most common solid organ neoplasm in children. Diagnostic dilemmas with small specimens from CNS...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Neurilemmomatosis

Lee SC, Chun IK, Kim YP

Neurilemmomatosis is a clinical entity consisting of multiple cutaneous neurilemmomas, central nervous system tumors, and neurologic disorders. Since Shishiba et al first described the disorder in 1984, several cases have...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Primary CNS Lymphoma Presenting as a Huge Intraventricular Mass

Jang MU, Hong HJ, Lee YK, Bae JS, Go SM, Park SS, Kim MK, Kim BJ

  • KMID: 1572323
  • J Korean Neurol Assoc.
  • 2006 Apr;24(2):178-180.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Epidemiology of Primary Brain and Central Nervous System Tumors in Korea

Lee CH, Jung KW, Yoo H, Park S, Lee SH

OBJECTIVE: The aim of this report is to provide accurate nationwide epidemiologic data on primary central nervous system (CNS) tumors in Korea. Despite its importance, there are no accurate statistics...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Chordoid Glioma : A Case Report of Unusual Location and Neuroradiological Characteristics

Kim JW, Kim JH, Choe G, Kim CY

Since the World Health Organization (WHO) classification for central nervous system neoplasms was declared in 2000, chordoid glioma of the third ventricle has been noted as a newly recognized tumor...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Neurilemmomatosis Associated with CNS Tumors

Yoon SY, Cho JH, Kang H, Lee JD, Cho SH

  • KMID: 1931211
  • Korean J Dermatol.
  • 2005 Sep;43(9):1277-1279.
Neurilemmomatosis is a clinical entity clearly distinguished from neurofibromatosis of von Recklinghausen's disease, and characteristically consists of multiple, cutaneuos neurilemmomas, central nervous system tumors, and neurologic disorders. A 52-year-old man,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Radiation Therapy against Pediatric Malignant Central Nervous System Tumors : Embryonal Tumors and Proton Beam Therapy

Lim DH

Radiation therapy is highly effective for the management of pediatric malignant central nervous system (CNS) tumors including embryonal tumors. With the increment of long-term survivors from malignant CNS tumors, the...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Cervical Ganglioglioma

Shin JJ, Oh SH, Yoon DH, Kim TS

  • KMID: 1956009
  • J Korean Neurosurg Soc.
  • 2001 Feb;30(2):239-243.
Gangliogliomas are benign tumors, composed of neoplastic astrocytes and nerve cells. They are rare, account for 0.4-6.25% of all primary central nervous system neoplasms. Gangliogliomas affect predominantly infants or young...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Current Status of Immunotherapeutic Strategies for Central Nervous System Tumors

Yang MY, Khan-Farooqi H, Prins RM, Liau LM

  • KMID: 2189078
  • J Korean Neurosurg Soc.
  • 2006 Oct;40(4):217-226.
Malignant gliomas are the most common type of primary brain tumor and are in great need of novel therapeutic approaches. Advances in treatment have been very modest, significant improvement in...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
The Status of Central Nervous System Tumors in Chonnam and Chonbuk Provinces

Yoon KS, Cho KY, Kim HI, Kim TY, Cho KG, Shin H, Kang SS, Woo JH

  • KMID: 2187725
  • J Korean Neurosurg Soc.
  • 1990 Jul;19(7):973-984.
The authors analized statistically 635 cases of pathologically confirmed central nervous system tumors in the Chonnam and Chonbuk provinces from 1987 to 1989. The results were as follows ; 1)...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Survival improvement with combined radio-chemotherapy in the primary central nervous system lymphomas

Wu HG, Kim IH, Ha SW, Park CI, Bang YJ, Huh DS

The benefits of radio-chemotherapy in HIV-negative primary central nervous system (CNS) lymphomas were analyzed in 40 patients, who received radiotherapy to the brain or craniospinal axis with the total dose...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Intracranial Cavernous Hemangioma after Radiotheraphy for Astrocytoma

Jung JM, Kim JS, Kim KJ, Hwang SH, Park IS, Kim ES, Han JW, Kim YK

  • KMID: 1812802
  • J Korean Neurosurg Soc.
  • 2001 Nov;30(11):1324-1327.
Radiation is a common treatment modality for central nervous system neoplasms. However, secondary tumor development must be considered in the differential diagnosis in patients with new or recurring symptoms after...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Extranodal Marginal Zone B-Cell Lymphoma of Mucosa-Associated Tissue Type Involving the Dura

Choi JY, Chung JH, Park YJ, Jung GY, Yoon TW, Kim YJ, Lim TK, Kim BS, Nam SH

Primary central nervous system marginal zone B-cell lymphoma (MZBCL) is very rare, with only a few reported cases worldwide. It has an indolent disease course with high cure potential. We...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Angiographic Characteristics of Central Neurocytoma Suggest the Origin of Tumor

Paek SH, Kim JE, Kim DG, Han MH, Jung HW

The authors retrospectively analyzed the angiographic findings performed in 17 cases with central neurocytoma to document the angiographic characteristics and suggested the origin of tumor based on the angiographic findings....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Cytogenetic Characterizations of Central Nervous System Tumors: The First Comprehensive Report from a Single Institution in Korea

Kim KE, Kim KU, Kim DC, Park JI, Han JY

The World Health Organization (WHO) classification of central nervous system (CNS) tumors incorporates morphology, cytogenetics, molecular genetics, and immunologic markers. Despite the relatively large number of CNS tumors with clonal...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Combination Therapy with Rituximab and Temozolomide for Recurrent and Refractory Primary Central Nervous System Lymphoma

Murakami M, Fujimaki T, Asano S, Nakaguchi , Yamada SM, Hoya K, Yamazaki K, Ishida Y, Matsuno A

High-dose methotrexate-based chemotherapy has extended survival in patients with primary central nervous system lymphoma (PCNSL). However, although salvage treatment is necessary in recurrent and refractory PCNSL, this has not been...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Intradural Extramedullary and Subcutaneous Tumors in Neonate : Atypical Myxoid Spindle Cell Neoplasm

Yu DW, Choi JH, Lee ES, Kim SH

Tumors of the central nervous system are common in the pediatric population and constitute the second most prevalent tumor type in children. Within this group, spinal cord tumors are relatively...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Central Nervous System Myelomatosis with Complex Chromosome Aberrations

Bang HI, Yoo JY, Kim KH, Park R, Shin JW, Choi TY, Lee SC, Park HS, Won JH

Involvement of the central nervous system is very uncommon in multiple myeloma, observed in approximately 1% of the multiple myeloma patients. We report a case of central nervous system myelomatosis...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Disseminated Hemangioblastomatosis of the Central Nervous System without von Hippel-Lindau Disease: A Case Report

Kim HR, Suh YL, Kim JW, Lee JI

We report a very rare case of hemangioblastomatosis that developed after surgical removal of a solitary cerebellar hemangioblastoma (HB). A 51-yr-old man presented with back pain 10 yr after undergoing...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Diencephalic syndrome: a frequently neglected cause of failure to thrive in infants

Kim A, Moon JS, Yang HR, Chang JY, Ko JS, Seo JK

PURPOSE: Diencephalic syndrome is an uncommon cause of failure to thrive in early childhood that is associated with central nervous system neoplasms in the hypothalamic-optic chiasmatic region. It is characterized...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr