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Hypoglossal schwannomas: A systematic review of the literature.
Bindal, Shivani; El Ahmadieh, Tarek Y; Plitt, Aaron; Aoun, Salah G; Neeley, Om James; El Tecle, Najib E; Barnett, Samuel; Gluf, Wayne.
Afiliação
  • Bindal S; Department of Neurological Surgery, The University of Texas Southwestern, Dallas, TX, United States.
  • El Ahmadieh TY; Department of Neurological Surgery, The University of Texas Southwestern, Dallas, TX, United States. Electronic address: tarek.elahmadieh@phhs.org.
  • Plitt A; Department of Neurological Surgery, The University of Texas Southwestern, Dallas, TX, United States.
  • Aoun SG; Department of Neurological Surgery, The University of Texas Southwestern, Dallas, TX, United States.
  • Neeley OJ; Department of Neurological Surgery, The University of Texas Southwestern, Dallas, TX, United States.
  • El Tecle NE; Department of Neurological Surgery, Saint Louis University Hospital, Saint Louis, MO, United States.
  • Barnett S; Department of Neurological Surgery, The University of Texas Southwestern, Dallas, TX, United States.
  • Gluf W; Department of Neurological Surgery, The University of Texas Southwestern, Dallas, TX, United States.
J Clin Neurosci ; 62: 162-173, 2019 Apr.
Article em En | MEDLINE | ID: mdl-30472335
ABSTRACT

BACKGROUND:

Schwannomas of the hypoglossal nerve are rare and account for a very small percentage of non-vestibular schwannomas.

OBJECTIVES:

In this systematic review of the literature, we examined the epidemiology, symptomatology, management, and outcomes of patients with hypoglossal schwannomas.

METHODS:

The electronic database Pubmed was searched for all reports of hypoglossal schwannomas with descriptions of symptoms, management, and outcome characteristics. Data was extracted from each study and compiled in a spreadsheet. Continuous variables were reported as means and medians. Categorical variables were reported as proportions. Additional analysis was not done due to inconsistent reporting of outcomes and small sample sizes.

RESULTS:

A total of 59 studies (94 total individual cases) were included. 64% of patients were female with mean age of 44.6 years. The majority were intracranial/extracranial (50%). The most common symptoms were tongue deviation or speech disturbance (38%) and headaches (33%). Hypoglossal nerve dysfunction was present in 80% of patients. Surgical excision was performed in 93%, with a 15% complication rate. Evidence of residual mass after surgery was noted in 29%. Permanent hypoglossal nerve deficits occurred in 67%. Recurrence of tumor burden was reported in 6 studies, with median time to recurrence of 16.5 months.

CONCLUSION:

Current evidence suggests overall favorable outcomes with surgical resection of hypoglossal schwannomas, with a large percentage of patients experiencing mild and usually well-tolerated neurologic deficit. Limitations of this study include the use of retrospective data taken from case reports/series with highly selected patients, selective reporting, and absence of control groups.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias dos Nervos Cranianos / Doenças do Nervo Hipoglosso / Neurilemoma Tipo de estudo: Systematic_reviews Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Clin Neurosci Assunto da revista: NEUROLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias dos Nervos Cranianos / Doenças do Nervo Hipoglosso / Neurilemoma Tipo de estudo: Systematic_reviews Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Clin Neurosci Assunto da revista: NEUROLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos