Literature DB >> 16130092

Edema is a precursor to central nervous system peritumoral cyst formation.

Russell R Lonser1, Alexander O Vortmeyer, John A Butman, Sven Glasker, Michael A Finn, Joshua M Ammerman, Marsha J Merrill, Nancy A Edwards, Zhengping Zhuang, Edward H Oldfield.   

Abstract

Despite the common occurrence and frequent clinical effects of peritumoral cysts in the central nervous system (CNS), the mechanism underlying their development and evolution is not understood. Because they commonly produce peritumoral cysts and because serial magnetic resonance imaging (MRI) is obtained in von Hippel-Lindau disease patients, hemangioblastomas provide an opportunity to examine the pathophysiology of CNS peritumoral cyst formation. Serial MRI was correlated with the clinical findings in 16 von Hippel-Lindau disease patients with 22 CNS hemangioblastomas (11 spinal cord; 11 cerebellar) that were associated with the appearance and evolution of peritumoral cysts. Hemangioblastoma-associated cyst wall histomorphological analysis was performed on postmortem tissues from three von Hippel-Lindau disease patients (not in the clinical series). Comparative proteomic profiling was performed on peritumoral cyst fluid and serum. Vascular endothelial growth factor levels were determined in peritumoral cysts. MRI clearly showed peritumoral edema that developed and slowly and progressively evolved into enlarging hemangioblastoma-associated cysts in all tumors (mean follow-up, 130 +/- 38 months; mean +/- standard deviation). Postcontrast MRI demonstrated convective leakage of gadolinium into cysts. Mean time required for edema to evolve into a cyst was 36 +/- 23 months (range, 8-72 months). Thirteen (59%) hemangioblastoma-cysts became symptomatic (mean time to symptom formation after cyst development, 35 +/- 32 months; range, 3-102 months) and required resection. Protein profiles of cyst fluid and serum were similar. Mean cyst fluid vascular endothelial growth factor concentration was 1.5 ng/ml (range, 0-5.4 ng/ml). Histology of the cyst walls was consistent with reactive gliosis. CNS peritumoral cyst formation is initiated by increased tumor vascular permeability, increased interstitial pressure in the tumor, and plasma extravasation with convective distribution into the surrounding tissue. When the delivery of plasma from the tumor exceeds the capacity of the surrounding tissue to absorb the extravasated fluid, edema (with its associated increased interstitial pressure) and subsequent cyst formation occur.

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Year:  2005        PMID: 16130092     DOI: 10.1002/ana.20584

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  28 in total

Review 1.  Vascular hyperpermeability as a hallmark of phacomatoses: is the etiology angiogenesis comparable with mechanisms seen in inflammatory pathways? Part I: historical observations and clinical perspectives on the etiology of increased CSF protein levels, CSF clotting, and communicating hydrocephalus: a comprehensive review.

Authors:  Yosef Laviv; Burkhard S Kasper; Ekkehard M Kasper
Journal:  Neurosurg Rev       Date:  2017-03-07       Impact factor: 3.042

2.  Biological and clinical impact of hemangioblastoma-associated peritumoral cysts in von Hippel-Lindau disease.

Authors:  Kristin Huntoon; Tianxia Wu; J Bradley Elder; John A Butman; Emily Y Chew; W Marston Linehan; Edward H Oldfield; Russell R Lonser
Journal:  J Neurosurg       Date:  2015-10-30       Impact factor: 5.115

3.  Characterization of the blood-brain barrier of metastatic and primary malignant neoplasms.

Authors:  Edjah K Nduom; Chunzhang Yang; Marsha J Merrill; Zhengping Zhuang; Russell R Lonser
Journal:  J Neurosurg       Date:  2013-04-26       Impact factor: 5.115

4.  Development of a small solid cerebellar haemangioblastoma into a large pseudocyst with a mural nodule in a patient without VHL; the importance of regular follow-up.

Authors:  Hansol Kim; Jin-Deok Joo; Young-Hoon Kim; Chae-Yong Kim
Journal:  BMJ Case Rep       Date:  2014-11-26

5.  Long-term outcome after resection of brainstem hemangioblastomas in von Hippel-Lindau disease.

Authors:  Joshua J Wind; Kamran D Bakhtian; Jennifer A Sweet; Gautam U Mehta; Jayesh P Thawani; Ashok R Asthagiri; Edward H Oldfield; Russell R Lonser
Journal:  J Neurosurg       Date:  2010-10-08       Impact factor: 5.115

6.  Blood-brain barrier. Response.

Authors:  Edjah K Nduom; Zhengping Zhuang; Russell R Lonser
Journal:  J Neurosurg       Date:  2014-01       Impact factor: 5.115

Review 7.  Application and implementation of selective tissue microdissection and proteomic profiling in neurological disease.

Authors:  Jay Jagannathan; Jie Li; Nicholas Szerlip; Alexander O Vortmeyer; Russell R Lonser; Edward H Oldfield; Zhengping Zhuang
Journal:  Neurosurgery       Date:  2009-01       Impact factor: 4.654

8.  Progressive peritumoral edema defining the optic fibers and resulting in reversible visual loss.

Authors:  Martin Baggenstos; Emily Chew; John A Butman; Edward H Oldfield; Russell R Lonser
Journal:  J Neurosurg       Date:  2008-08       Impact factor: 5.115

9.  Pathological satiety caused by brainstem hemangioblastoma.

Authors:  Debbie K Song; Russell R Lonser
Journal:  J Neurosurg Pediatr       Date:  2008-12       Impact factor: 2.375

10.  Protracted haemangioblastic proliferation and differentiation in von Hippel-Lindau disease.

Authors:  S B Shively; S Beltaifa; B Gehrs; H Duong; J Smith; N A Edwards; Rr Lonser; M Raffeld; A O Vortmeyer
Journal:  J Pathol       Date:  2008-12       Impact factor: 7.996

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