Retinal astrocytic tumors

Christopher Seungkyu Lee, Sungchul Lee, Arun D. Singh

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Retinal astrocytic tumors are benign tumors representing two clinical types: astrocytic hamartoma and “acquired” retinal astrocytoma. Retinal astrocytic hamartomas are frequently associated with tuberous sclerosis complex (TSC). “Acquired” retinal astrocytomas are rare astrocytic tumors that develop in somewhat older individuals who have no clinical manifestations of TSC or other systemic syndromes.

Original languageEnglish
Title of host publicationClinical Ophthalmic Oncology
Subtitle of host publicationRetinal Tumors
PublisherSpringer Berlin Heidelberg
Pages35-44
Number of pages10
ISBN (Electronic)9783642394898
ISBN (Print)9783642394881
DOIs
Publication statusPublished - 2014 Jan 1

Fingerprint

Retinal Neoplasms
Tuberous Sclerosis
Hamartoma
Astrocytoma
Neoplasms

All Science Journal Classification (ASJC) codes

  • Medicine(all)

Cite this

Lee, C. S., Lee, S., & Singh, A. D. (2014). Retinal astrocytic tumors. In Clinical Ophthalmic Oncology: Retinal Tumors (pp. 35-44). Springer Berlin Heidelberg. https://doi.org/10.1007/978-3-642-39489-8_4
Lee, Christopher Seungkyu ; Lee, Sungchul ; Singh, Arun D. / Retinal astrocytic tumors. Clinical Ophthalmic Oncology: Retinal Tumors. Springer Berlin Heidelberg, 2014. pp. 35-44
@inbook{624e81c91c774838959f436511c06727,
title = "Retinal astrocytic tumors",
abstract = "Retinal astrocytic tumors are benign tumors representing two clinical types: astrocytic hamartoma and “acquired” retinal astrocytoma. Retinal astrocytic hamartomas are frequently associated with tuberous sclerosis complex (TSC). “Acquired” retinal astrocytomas are rare astrocytic tumors that develop in somewhat older individuals who have no clinical manifestations of TSC or other systemic syndromes.",
author = "Lee, {Christopher Seungkyu} and Sungchul Lee and Singh, {Arun D.}",
year = "2014",
month = "1",
day = "1",
doi = "10.1007/978-3-642-39489-8_4",
language = "English",
isbn = "9783642394881",
pages = "35--44",
booktitle = "Clinical Ophthalmic Oncology",
publisher = "Springer Berlin Heidelberg",

}

Lee, CS, Lee, S & Singh, AD 2014, Retinal astrocytic tumors. in Clinical Ophthalmic Oncology: Retinal Tumors. Springer Berlin Heidelberg, pp. 35-44. https://doi.org/10.1007/978-3-642-39489-8_4

Retinal astrocytic tumors. / Lee, Christopher Seungkyu; Lee, Sungchul; Singh, Arun D.

Clinical Ophthalmic Oncology: Retinal Tumors. Springer Berlin Heidelberg, 2014. p. 35-44.

Research output: Chapter in Book/Report/Conference proceedingChapter

TY - CHAP

T1 - Retinal astrocytic tumors

AU - Lee, Christopher Seungkyu

AU - Lee, Sungchul

AU - Singh, Arun D.

PY - 2014/1/1

Y1 - 2014/1/1

N2 - Retinal astrocytic tumors are benign tumors representing two clinical types: astrocytic hamartoma and “acquired” retinal astrocytoma. Retinal astrocytic hamartomas are frequently associated with tuberous sclerosis complex (TSC). “Acquired” retinal astrocytomas are rare astrocytic tumors that develop in somewhat older individuals who have no clinical manifestations of TSC or other systemic syndromes.

AB - Retinal astrocytic tumors are benign tumors representing two clinical types: astrocytic hamartoma and “acquired” retinal astrocytoma. Retinal astrocytic hamartomas are frequently associated with tuberous sclerosis complex (TSC). “Acquired” retinal astrocytomas are rare astrocytic tumors that develop in somewhat older individuals who have no clinical manifestations of TSC or other systemic syndromes.

UR - http://www.scopus.com/inward/record.url?scp=84956503105&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84956503105&partnerID=8YFLogxK

U2 - 10.1007/978-3-642-39489-8_4

DO - 10.1007/978-3-642-39489-8_4

M3 - Chapter

SN - 9783642394881

SP - 35

EP - 44

BT - Clinical Ophthalmic Oncology

PB - Springer Berlin Heidelberg

ER -

Lee CS, Lee S, Singh AD. Retinal astrocytic tumors. In Clinical Ophthalmic Oncology: Retinal Tumors. Springer Berlin Heidelberg. 2014. p. 35-44 https://doi.org/10.1007/978-3-642-39489-8_4