Sporadic Hemangioblastoma in the Pituitary Stalk: A Case Report and Review of the Literature
Hemangioblastomas in the pituitary stalk are especially rare. Most pituitary stalk hemangioblastomas reported in the literature were associated with von Hippel-Lindau (VHL) disease. Here, we report only the 3rd case of sporadic pituitary stalk hemangioblastoma diagnosed in a 60-year-old woman. Despi...
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Published in | Journal of Korean Neurosurgical Society Vol. 57; no. 6; pp. 465 - 468 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Korea (South)
The Korean Neurosurgical Society
01.06.2015
대한신경외과학회 |
Subjects | |
Online Access | Get full text |
ISSN | 2005-3711 1598-7876 |
DOI | 10.3340/jkns.2015.57.6.465 |
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Abstract | Hemangioblastomas in the pituitary stalk are especially rare. Most pituitary stalk hemangioblastomas reported in the literature were associated with von Hippel-Lindau (VHL) disease. Here, we report only the 3rd case of sporadic pituitary stalk hemangioblastoma diagnosed in a 60-year-old woman. Despite the danger of potential complications due to excessive vascularity or proximity to important neural structures, the tumor in our case was successfully removed while preserving pituitary function. In this case, complete surgical excision was shown to be an effective treatment option for symptomatic pituitary stalk hemangioblastoma, and we suggest careful evaluation of any highly enhancing mass with a signal void in the pituitary stalk preoperatively, even if no VHL disease is evident. |
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AbstractList | Hemangioblastomas in the pituitary stalk are especially rare. Most pituitary stalk hemangioblastomas reported in the literature were associated with von Hippel-Lindau (VHL) disease. Here, we report only the 3rd case of sporadic pituitary stalk hemangioblastoma diagnosed in a 60-year-old woman. Despite the danger of potential complications due to excessive vascularity or proximity to important neural structures, the tumor in our case was successfully removed while preserving pituitary function. In this case, complete surgical excision was shown to be an effective treatment option for symptomatic pituitary stalk hemangioblastoma, and we suggest careful evaluation of any highly enhancing mass with a signal void in the pituitary stalk preoperatively, even if no VHL disease is evident.Hemangioblastomas in the pituitary stalk are especially rare. Most pituitary stalk hemangioblastomas reported in the literature were associated with von Hippel-Lindau (VHL) disease. Here, we report only the 3rd case of sporadic pituitary stalk hemangioblastoma diagnosed in a 60-year-old woman. Despite the danger of potential complications due to excessive vascularity or proximity to important neural structures, the tumor in our case was successfully removed while preserving pituitary function. In this case, complete surgical excision was shown to be an effective treatment option for symptomatic pituitary stalk hemangioblastoma, and we suggest careful evaluation of any highly enhancing mass with a signal void in the pituitary stalk preoperatively, even if no VHL disease is evident. Hemangioblastomas in the pituitary stalk are especially rare. Most pituitary stalk hemangioblastomas reported in the literature were associated with von Hippel-Lindau (VHL) disease. Here, we report only the 3rd case of sporadic pituitary stalk hemangioblastoma diagnosed in a 60-year-old woman. Despite the danger of potential complications due to excessive vascularity or proximity to important neural structures, the tumor in our case was successfully removed while preserving pituitary function. In this case, complete surgical excision was shown to be an effective treatment option for symptomatic pituitary stalk hemangioblastoma, and we suggest careful evaluation of any highly enhancing mass with a signal void in the pituitary stalk preoperatively, even if no VHL disease is evident. KCI Citation Count: 5 Hemangioblastomas in the pituitary stalk are especially rare. Most pituitary stalk hemangioblastomas reported in the literature were associated with von Hippel-Lindau (VHL) disease. Here, we report only the 3rd case of sporadic pituitary stalk hemangioblastoma diagnosed in a 60-year-old woman. Despite the danger of potential complications due to excessive vascularity or proximity to important neural structures, the tumor in our case was successfully removed while preserving pituitary function. In this case, complete surgical excision was shown to be an effective treatment option for symptomatic pituitary stalk hemangioblastoma, and we suggest careful evaluation of any highly enhancing mass with a signal void in the pituitary stalk preoperatively, even if no VHL disease is evident. |
Author | Choi, Kyu-Sun Kim, Choong-Hyun Lee, Gun-Ill Kim, Jae-Min |
AuthorAffiliation | Department of Neurosurgery, Hanyang University Guri Hospital, Guri, Korea |
AuthorAffiliation_xml | – name: Department of Neurosurgery, Hanyang University Guri Hospital, Guri, Korea |
Author_xml | – sequence: 1 givenname: Gun-Ill surname: Lee fullname: Lee, Gun-Ill organization: Department of Neurosurgery, Hanyang University Guri Hospital, Guri, Korea – sequence: 2 givenname: Jae-Min surname: Kim fullname: Kim, Jae-Min organization: Department of Neurosurgery, Hanyang University Guri Hospital, Guri, Korea – sequence: 3 givenname: Kyu-Sun surname: Choi fullname: Choi, Kyu-Sun organization: Department of Neurosurgery, Hanyang University Guri Hospital, Guri, Korea – sequence: 4 givenname: Choong-Hyun surname: Kim fullname: Kim, Choong-Hyun organization: Department of Neurosurgery, Hanyang University Guri Hospital, Guri, Korea |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26180617$$D View this record in MEDLINE/PubMed https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002012014$$DAccess content in National Research Foundation of Korea (NRF) |
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CitedBy_id | crossref_primary_10_1097_PAP_0000000000000176 crossref_primary_10_1016_j_wneu_2018_03_114 crossref_primary_10_14791_btrt_2019_7_e40 crossref_primary_10_7759_cureus_9107 crossref_primary_10_1016_j_clineuro_2018_03_010 crossref_primary_10_1055_s_0041_1734335 |
Cites_doi | 10.3171/jns.1968.28.4.0365 10.2214/ajr.180.5.1801480 10.1007/BF01402059 10.1016/0090-3019(84)90010-7 10.1016/j.clineuro.2006.11.007 10.1227/00006123-199402000-00021 10.1016/0140-6736(91)91705-Y 10.3171/jns.1996.84.6.1046 10.3340/jkns.2013.53.5.297 10.1016/j.surneu.2006.08.073 10.1017/S0317167100010945 10.1016/S0090-3019(01)00482-7 10.3171/2008.4.17532 10.3171/jns.1989.70.1.0024 |
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Keywords | Pituitary stalk Hemangioblastoma Suprasellar tumor |
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