- A Case of Bilateral Optic Nerve Glioma
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Lee GH, Huh W
- KMID: 1949137
- J Korean Ophthalmol Soc.
- 1987 Feb;28(1):223-227.
Optic nerve gliomas are uncommon, and they and derived from altrocyte or oligodendrocyte of the optic nerve. The peak incidence is from 2 to 6 years of age. In most... -
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- Glioma of the Optic Nerve and Optic Chiasm
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Hong KS, Han WS, Kim OK
- KMID: 1967561
- Ewha Med J.
- 1984 Jun;7(2):107-110.
- doi: 10.12771/emj.1984.7.2.107
Most optic gliomas are benign astrocytomas that might better be considered hamartomas than true neoplasms. Optic gliomas rerely becomemalignant and their morbidity is mainly due to enlargement of the tumor.... -
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- Optic Nerve Glioma: A Case of Surgical Treatment to the Optic Chiasm Tumor
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Jang HJ, Min EJ, Park BI
- KMID: 2204984
- J Korean Ophthalmol Soc.
- 1991 May;32(5):397-400.
A twenty nine-year-old woman has suffered for ten years from progressive proptosis and loss of vision in the right eye. Her right eye had deviated out-and-upwards, and its visual acuity... -
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- Optic Neuritis Mimicking Ischemic Optic Neuropathy and Optic Glioma
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Kang EM, Kwon KY, Choi MJ, Kim CY, Seong GJ, Hong S
- KMID: 2216625
- J Korean Ophthalmol Soc.
- 2014 Nov;55(11):1721-1725.
- doi: 10.3341/jkos.2014.55.11.1721
PURPOSE: To report a case of optic neuritis difficult to differentiate from ischemic optic neuropathy and optic nerve glioma. CASE SUMMARY: A 63-year-old male visited our clinic because of a sudden... -
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- A Case of Optic Nerve Glioma
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Lee SH, Kim JJ, Jo JC
- KMID: 1948589
- J Korean Ophthalmol Soc.
- 1968 Dec;9(4):27-31.
A case of optic nerve glioma is presented. This 11 years old Korean boy was seen because of proto nasion of the risht eye ball of 2 months duration. Vision... -
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- A Case of Optic Nerve Glioma
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Lee YH, Lee MJ, Shyn KH
- KMID: 2042578
- J Korean Ophthalmol Soc.
- 1986 Dec;27(6):1121-1125.
Gliomas of the optic nerve are relatively uncommon. We have experienced one case of glioma of the optic nerve recently. The patient was 17 year old boy who had exophthalmos... -
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- Neurofibromatosis Type 1 with Cerebellar Piloytic Astrocytoma
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Jeon IS, Kim JS, Kim JH, Kim NR
- KMID: 1654707
- Korean J Pediatr.
- 2004 Apr;47(4):458-461.
Neurofibromatosis type 1(NF1) is one of the most common inherited disorders, clinically characterized by cafe-au-lait spots, Lisch nodules and neurofibromas. In addition, the affected individuals usually develop benign and malignant... -
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- Clinical Characteristics, Including Endocrinological Changes, of Optic Glioma in Children
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Yu JS, Kim SY, Shin CH, Kim KJ, Yang SW, Hwang YS
- KMID: 2335373
- J Korean Pediatr Soc.
- 1998 Aug;41(8):1111-1119.
PURPOSE: Optic glioma is a primary tumor arising from the optic nerve and/or chiasm. When located in the hypothalamus, it can produce endocrine signs such as diencephalic syndrome, diabetes insipidus,... -
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- Fractionated Stereotactic Radiosurgery(FSRS) for Sella and Parasella Tumors Adjacent to Optic Apparatus
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Park HJ, Yee GT, Choi CY, Sohn MJ, Lee DJ, Whang CJ
- KMID: 1588437
- J Korean Neurosurg Soc.
- 2004 Oct;36(4):281-285.
OBJECTIVE: Compared with other neural structures, optic apparatus are particularly sensitive to radiation. If tumors are adjacent to or in contact with optic apparatus, a number of limitations need to... -
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- Ophthalmic Manifestations in Patients With Neurofibromatosis
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Bang J, Yang HS, Ahn JH, Kook KH, Chang YH
- KMID: 2337743
- J Korean Ophthalmol Soc.
- 2008 Nov;49(11):1829-1838.
PURPOSE: To report the ophthalmic manifestations of neurofibromatosis in Korea. METHODS: Ophthalmologic examinations were performed from November 2001 to January 2008 for 153 consecutive patients who were diagnosed with neurofibromatosis according... -
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- Glioblastoma in a Patient with Neurofibromatosis Type 1: A Case Report and Review of the Literature
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Jeong TS, Yee GT
- KMID: 1734666
- Brain Tumor Res Treat.
- 2014 Apr;2(1):36-38.
- doi: 10.14791/btrt.2014.2.1.36
Neurofibromatosis type 1 (NF1) is an autosomal dominantly inherited familial tumor syndrome. Benign tumors such as pilocytic astrocytoma, optic glioma make up the majority of intracranial neoplasms in patients with... -
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- A Case of Radiologically Suspected Mesenteric Plexiform Neurofibromas in a Patient with Type I Neurofibromatosis
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Oh SM, Kim YO, Son YJ, Woo YJ
- KMID: 2329433
- J Korean Child Neurol Soc.
- 2009 Nov;17(2):226-230.
Neurofibromatosis type I(NF-1) is an autosomal dominant neurocutaneous syndrome characterized by cafe-au-lait spots, optic glioma, skeletal dysplasia, and iris hamartoma. Mesenteric plexiform neurofibromas(PNF) have been rarely reported in NF-1, especially... -
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- An orbital hemangioendothelioma of fetus detected by prenatal ultrasonography
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Bae JG, Lim SY, Rhee JH, Kim JI, Park JC
- KMID: 2274068
- Korean J Obstet Gynecol.
- 2011 Aug;54(8):464-467.
- doi: 10.5468/KJOG.2011.54.8.464
Most orbital tumors of infants include retinoblastoma, dermoid cyst (teratoma), optic nerve glioma and nevus, and hemangioendothelioma is found in rare cases. Hemangioendothelioma, the tumor of intermediate malignancy between angiosarcoma... -
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- A Novel c.6766_6767insAA Mutation in the Neurofibromin Gene in a Patient with Neurofibromatosis Type 1-Associated Glioblastoma
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Yang EH, Kim YM, Kim KJ, Cha SH, Kwak MJ
- KMID: 2435231
- J Korean Child Neurol Soc.
- 2018 Sep;26(3):175-179.
- doi: 10.26815/jkcns.2018.26.3.175
Neurofibromatosis type 1 (NF-1) is an autosomal dominant neurocutaneous syndrome caused by mutations in the neurofibromin gene. NF-1 patients have a high risk of tumors, and optic glioma is the... -
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- Optochiasmatic Cavernous Angioma with Rapid Progression after Biopsy Despite Radiation Therapy
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Jo KW, Kim SD, Chung EY, Park IS
- KMID: 1442619
- J Korean Neurosurg Soc.
- 2011 Feb;49(2):120-123.
- doi: 10.3340/jkns.2011.49.2.120
We present a rare case of optochiasmatic cavernous angioma (CA) that progressed despite radiation therapy. A 31-year-old female patient presented with sudden loss of left visual acuity and right homonymous... -
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- Computed tomography of orbital diseases in childhood
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Kim OH, Lee JM, Bahk YW
- KMID: 2462387
- J Korean Radiol Soc.
- 1985 Dec;21(6):883-892.
- doi: 10.3348/jkrs.1985.21.6.883
We anlized CT of 29 cases of various orbital disease in pediatric age group. Diagnoses were confirmed byeither operation or direct ophthalmoscopy. The patients were examined during the period of... -
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- A Case of Colon Cancer in a Patient with Neurofibromatosis Type I
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Kim KJ, Choi SR, Sohn SH, Lee S, Hong KB, Keum DJ, Jee SR, Lee JH, Han SY, Shin WW
- KMID: 1864985
- Korean J Gastroenterol.
- 2002 Dec;40(6):402-405.
Neurofibromatosis type I is an autosomal dominant disorder that occurs once in 3,000 births. It is characterized by neurofibromas and caf au lait spots of the skin. Neurofibromatosis type... -
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- A Case of Neurofibromatosis Type I with Moyamoya Syndrome and Ganglioneuroma in Lung
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Sim JY, Lim JS, Han YS, Kim JY, Kim WS
- KMID: 2329432
- J Korean Child Neurol Soc.
- 2009 Nov;17(2):221-225.
Neurofibromatosis type I is one of the most common neurocutaneous syndrome which is inherited by autosomal dominant manner, characterized by cafe au-lait spots, axillary freckling, Lisch nodules in iris, multiple... -
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- Solitary Pigmented Plexiform Neurofibroma in Lower Eyelid: A Case Report
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Yoon HJ, Yoon KC, Kim GE, Choi W
- KMID: 2371915
- J Korean Ophthalmol Soc.
- 2017 Mar;58(3):333-336.
- doi: 10.3341/jkos.2017.58.3.333
PURPOSE: Solitary plexiform neurofibroma of the eyelid without neurofibromatosis is a rare disease. We report a case of solitary plexiform pigmented neurofibroma of the eyelid without neurofibromatosis. CASE SUMMARY: A 12-year-old... -
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- A Case of Moyamoya Disease with Neurofibromatosis Type I
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Lee MA, Eum JP, Lee HY, Cha BH
- KMID: 2279609
- Korean J Pediatr.
- 2005 Jan;48(1):93-96.
Neurofibromatosis type I is an autosomal dominant disorder with varied manifestations in bone, soft tissue, the nervous system and skin. This is characterized by cafe-au-lait spots, neurofibromas, Lisch nodules, optic... -
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