Surgical resection of sporadic and hereditary hemangioblastoma: Our 10-year experience and a literature review

URN to cite this document:

urn:nbn:de:bvb:355-epub-314123 Copy

Bründl, Elisabeth ; Schoedl, Petra ; Odo-Winfried, Ullrich ; Brawanski, Alexander ; Schebesch, Karl-Michael

Preview

PDF (670kB)

Date of publication of this fulltext: 04 Mar 2015 09:00

---

Alternative links to fulltext:DOIPubmedPublisher

---

Details

Item type:	Article
Journal or Publication Title:	Surgeal Neurology International
Publisher:	SNI
Volume:	5
Number of Issue or Book Chapter:	1
Page Range:	p. 138
Date:	22 September 2014
Institutions:	Medicine > Lehrstuhl für Neurochirurgie
Projects:	Open Access Publizieren (DFG)
Identification Number:	Value Type 10.4103/2152-7806.141469 DOI 25317353 PubMed ID
Keywords:	CNS hemangioblastoma, neurological outcome, posterior cranial fossa, von Hippel–Lindau disease
Dewey Decimal Classification:	600 Technology > 610 Medical sciences Medicine
Status:	Published
Refereed:	Yes, this version has been refereed
Created at the University of Regensburg:	Yes
Item ID:	31412

Preview

Export bibliographical data

ASCII CitationAtomBibTeXData Cite XMLDataCite XML OAIDublin CoreEndNoteHTML CitationMETSMODSOpenAPCRDF+N-TriplesRDF+N3RDF+XMLReferReference ManagerSimple MetadataXMLxMetaDissPlus

---

Abstract

Background: Hemangioblastomas (HBLs) are benign neoplasms that contribute to 1-2.5% of intracranial tumors and 7-12% of posterior fossa lesions in adult patients. HBLs either evolve hereditarily in association with von Hippel-Lindau disease (vHL) or, more prevalently, as solitary sporadic tumors. Only few authors have reported on the clinical presentation and the neurological outcome of HBL. ...

Abstract

Background: Hemangioblastomas (HBLs) are benign neoplasms that contribute to 1-2.5% of intracranial tumors and 7-12% of posterior fossa lesions in adult patients. HBLs either evolve hereditarily in association with von Hippel-Lindau disease (vHL) or, more prevalently, as solitary sporadic tumors. Only few authors have reported on the clinical presentation and the neurological outcome of HBL. Methods: We retrospectively analyzed the clinical, radiological, surgical, and histopathologic records of 24 consecutive patients (11 men, 13 women; mean age 51.3 years) with HBL of the posterior cranial fossa, who had been treated at our center between 2001 and 2012. We reviewed the current literature, and discussed our findings in the context of previous publications on HBL. The study protocol was approved by the local ethics committee (14-101-0070). Results: Mean time to diagnosis was 14 weeks. The extent of resection (EOR) was total in 20 and near total in 4 patients. Four patients required revision within 24 h because of relevant postoperative bleeding. One patient died within 14 days. One patient required permanent shunting. At discharge, 75% of patients [n = 18, modified Rankin scale (mRS) 0-1] showed no or at least resolved symptoms. Mean follow-up was 21 months. Two recurrences were detected during follow-up. Conclusions: In comparison to other benign entities of the posterior fossa, time to diagnosis was significantly shorter for HBL. This finding indicates the rather aggressive biological behavior of these excessively vascularized tumors. In our series, however, the rate of complete resection was high, and morbidity and mortality rates were within the reported range.

---

---

Metadata last modified: 02 Jun 2018 05:42

Owner only: item control page

Download Statistics

Download Statistics

Download Statistics

Download Statistics

Downloads

Downloads per month over past year

Altmetric

Altmetric

Altmetric

Alternative Statistics (altmetrics)

More literature (via CORE)

More literature (via CORE)

More literature (via CORE)

More literature (via CORE)