Systematic scoping review of papilledema in vestibular schwannoma without hydrocephalus

被引:4
|
作者
Mishra, Rakesh [1 ]
Konar, Subhas Kanti [2 ]
Shrivastava, Adesh [3 ]
Agrawal, Amit [3 ]
Nair, Suresh [4 ]
机构
[1] Banaras Hindu Univ, Inst Med Sci, Dept Neurosurg, Varanasi, Uttar Pradesh, India
[2] Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurosurg, Bengaluru, India
[3] All India Inst Med Sci AIIMS, Dept Neurosurg, Bhopal 462020, India
[4] Sree Chitra Tirunal Inst Med Sci, Dept Neurosurg, Trivandrum, Kerala, India
关键词
Vestibular schwannoma; papilledema; ventriculomegaly; optic nerve sheath fenestration; visual loss; hyperproteinorrhachia; CSF proteins; hydrocephalus; OPTIC DISC EDEMA; PRESSURE;
D O I
10.1080/02688697.2022.2039376
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Vestibular schwannoma is a common pathology encountered by neurosurgeons worldwide. Often vestibular schwannoma presents with obstructive hydrocephalus. Papilledema is present in 8% of the patients with vestibular schwannoma, primarily due to obstructive hydrocephalus. Hyperproteinorrhachia is believed to be responsible for papilledema in the absence of hydrocephalus in vestibular schwannoma. However, there is a paucity of literature on the mechanism of papilledema in vestibular schwannoma patients with hydrocephalus. Objective The aim of this study was to conduct a scoping review of scientific literature on papilledema in vestibular schwannoma patients without hydrocephalus. Methods Design: This was a systematic scoping review and critical appraisal. Literature Search from PubMed was done following PRISMA-ScR (Preferred Reporting Items for Systematic Reviews and Meta-Analyses Extension for Scoping Reviews) and Joanna Briggs Institute guidelines for conducting and reporting scoping reviews. Results A total of seven studies, including eight patients, were identified for inclusion in the review. The studies were heterogeneous in terms of reporting for various variables. All the included studies were case reports, with the earliest publication in 1954 and the latest publication in 2020. The mean age of the patients in the included studies was 35 years, with a minimum age of 20 years and maximum age of 64 years. Approximately 62.5% were females, and 37.5% were males in the included study. Only three studies have studied cerebrospinal fluid (CSF) proteins levels in these patients. Conclusions There is paucity in literature and a lack of evidence to conclusively state hyperproteinorrhachia as an antecedent to the development of papilledema in vestibular schwannoma patients without hydrocephalus. Younger age and female gender are risk factors for developing papilledema in the absence of hydrocephalus in vestibular schwannoma patients. Brainstem compression due to the large size of vestibular schwannoma can still have a patent aqueduct of Sylvius and no obstruction to CSF flow. The development of papilledema in vestibular schwannoma is a complex interplay of multiple factors that must be studied comprehensively for complete understanding.
引用
收藏
页码:127 / 136
页数:10
相关论文
共 50 条
  • [31] Vestibular Rehabilitation: Improving Symptomatic and Functional Outcomes of Persons With Vestibular Schwannoma: A Systematic Review
    Yap, Jayden
    Palmer, Gretta
    Graving, Kate
    Stone, Shona
    Gane, Elise M.
    PHYSICAL THERAPY, 2024, 104 (10):
  • [32] Characteristics and management of hydrocephalus associated with vestibular schwannomas: a systematic review
    Paolo di Russo
    Arianna Fava
    Alberto Vandenbulcke
    Akinori Miyakoshi
    Michihiro Kohno
    Alexander I. Evins
    Vincenzo Esposito
    Roberta Morace
    Neurosurgical Review, 2021, 44 : 687 - 698
  • [33] Characteristics and management of hydrocephalus associated with vestibular schwannomas: a systematic review
    di Russo, Paolo
    Fava, Arianna
    Vandenbulcke, Alberto
    Miyakoshi, Akinori
    Kohno, Michihiro
    Evins, Alexander, I
    Esposito, Vincenzo
    Morace, Roberta
    NEUROSURGICAL REVIEW, 2021, 44 (02) : 687 - 698
  • [34] Reported Hearing Outcome Measures Following Stereotactic Radiosurgery for Vestibular Schwannoma: A Scoping Review
    Almufarrij, Ibrahim
    Hannan, Cathal John
    King, Andrew Thomas
    Vail, Andy
    Heal, Calvin
    Whitfield, Gillian
    Pathmanaban, Omar Nathan
    Lloyd, Simon K. K.
    Munro, Kevin J. J.
    JOURNAL OF NEUROLOGICAL SURGERY PART B-SKULL BASE, 2024, 85 (02) : 123 - 130
  • [35] A Scoping Review on Vestibulopathy After Microsurgical Resection of Vestibular Schwannoma-The Forgotten Symptom
    Bambakidis, Evangeline
    Mowry, Sarah
    Amin-Hanjani, Sepideh
    NEUROSURGERY PRACTICE, 2024, 5 (04):
  • [36] Translabyrinthine Excision of Vestibular Schwannoma with Concurrent Cochlear Implantation: Systematic Review
    Thompson, Nicholas J.
    O'Connell, Brendan P.
    Brown, Kevin D.
    JOURNAL OF NEUROLOGICAL SURGERY PART B-SKULL BASE, 2019, 80 (02) : 187 - 195
  • [37] Cochlear Implant Outcomes Following Vestibular Schwannoma Resection: Systematic Review
    Wick, Cameron C.
    Butler, Margaret J.
    Yeager, Lauren H.
    Kallogjeri, Dorina
    Durakovic, Nedim
    McJunkin, Jonathan L.
    Shew, Matthew A.
    Herzog, Jacques A.
    Buchman, Craig A.
    OTOLOGY & NEUROTOLOGY, 2020, 41 (09) : 1190 - 1197
  • [38] Hearing preservation after stereotactic radiosurgery for vestibular schwannoma: A systematic review
    Yang, Isaac
    Aranda, Derrick
    Han, Seunggu J.
    Chennupati, Sravana
    Sughrue, Michael E.
    Cheung, Steven W.
    Pitts, Lawrence H.
    Parsa, Andrew T.
    JOURNAL OF CLINICAL NEUROSCIENCE, 2009, 16 (06) : 742 - 747
  • [39] Cost of Vestibular Schwannoma Treatment: A Systematic Review and Meta-Analysis
    Koester, Stefan W.
    Dambrino, Robert J.
    Bhamidipati, Akshay
    Wong, Gunther
    Liles, Campbell
    Feldman, Michael
    Chambless, Lola B.
    JOURNAL OF NEUROLOGICAL SURGERY PART B-SKULL BASE, 2024, 85 (06) : 659 - 665
  • [40] A case of hydrocephalus associated with vestibular schwannoma, treated by tumor removal
    Kanayama, S
    Kohno, M
    Okamura, K
    Yoshino, M
    Segawa, H
    Saito, I
    Sano, K
    NEUROLOGICAL SURGERY, 2006, 34 (04): : 391 - 395