Literature DB >> 20737358

Meningiomas involving the sphenoid wing outcome after microsurgical treatment--a clinical review of 73 cases.

S Honig1, C Trantakis, B Frerich, I Sterker, R-D Kortmann, J Meixensberger.   

Abstract

OBJECTIVE: Sphenoid wing meningiomas represent a difficult to access subtype of intracranial meningiomas involving important neurovascular structures such as the optic nerve, cavernous sinus or carotid artery. They cause neurological compromises by direct compression of adjacent cranial nerves. Insidious and aggressive dural, bony, and orbital involvement produces several difficulties for adequate resection leading to higher rates of recurrence.
METHODS: This retrospective case analysis consists of 73 patients who were surgically treated for meningiomas involving the sphenoid wing, where a pterional approach was performed between April 2001 and February 2006. 51 women and 22 men with a mean age of 59.4 years were operated on. The follow-up period ranged from 3-75 months (mean 29.8 months). Patients were divided into the following groups based on the site of the tumor: group 1: outer part of the sphenoid ridge (lateral, n=16); group 2: middle part of the sphenoid ridge (intermediate, n=5); group 3: inner part of the sphenoid ridge (medial, n=22); and group 4: spheno-orbital meningioma (n=30).
RESULTS: The majority of patients presented with visual impairment (55%), followed by generalized headaches (36%) and visual field defects (33%). Total microscopic tumor resection was achieved in 35 patients (47.9%). Visual acuity improved in 58% of the patients, with 23% returning to normal vision. Preexisting cranial nerve deficits remained unchanged in the majority of patients (79%) and improved in 18%. Temporary new cranial nerve deficits occurred in 6 cases, and 1 patient (1%) developed permanent third nerve palsy. The mortality rate was 3% (2 patients) and the rate of permanent nonvisual morbidity was 7% (5 patients). 12 patients (16%) received postoperative radiotherapy. In 6 of 7 patients who were observed for at least 1 year after radiotherapy, stable tumor volume was noted at the follow-up review (mean 30.2 months, range 16-50 months), which provides a tumor growth control rate of 86%. The overall recurrence rate was 15% (11 of 73 patients).
CONCLUSION: The result of this study affirms the safety of microsurgical treatment strategies, so that sufficient tumor control can be achieved with minimal morbidity and satisfying functional results in most cases. © Georg Thieme Verlag KG Stuttgart · New York.

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Mesh:

Year:  2010        PMID: 20737358     DOI: 10.1055/s-0030-1261945

Source DB:  PubMed          Journal:  Cent Eur Neurosurg        ISSN: 1868-4904


  6 in total

1.  Impaired survival and long-term neurological problems in benign meningioma.

Authors:  Hanna van Alkemade; Michelle de Leau; Edith M T Dieleman; Jan W P F Kardaun; Rob van Os; W Peter Vandertop; Wouter R van Furth; Lukas J A Stalpers
Journal:  Neuro Oncol       Date:  2012-03-09       Impact factor: 12.300

2.  Sphenoid wing meningiomas: peritumoral brain edema as a prognostic factor in surgical outcome.

Authors:  Abdalrahman Nassar; Volodymyr Smolanka; Andriy Smolanka; Dipak Chaulagain; Oleg Devinyak
Journal:  Neurosurg Rev       Date:  2022-05-27       Impact factor: 2.800

3.  [Modern surgery of meningiomas affecting anterior visual pathways].

Authors:  F Grimm; F H Ebner; J Honegger
Journal:  Ophthalmologe       Date:  2013-05       Impact factor: 1.059

4.  Incidence, Clinico-Radiological Features and Outcome of Skull Base versus Non-Skull Base Meningiomas Treated in Kuala Lumpur General Hospital: A Five-Year Experience.

Authors:  Chan Chee Kong; Regunath Kandasamy; Saffari Haspani; Zamzuri Idris; Jafri Malin Abdullah
Journal:  Malays J Med Sci       Date:  2018-06-28

5.  Surgical Outcomes of Sphenoid Wing Meningioma with Periorbital Invasion.

Authors:  Ga-On Park; Hyun Ho Park; Jihwan Yoo; Chang-Ki Hong; Jiwoong Oh
Journal:  J Korean Neurosurg Soc       Date:  2022-03-03

6.  High-grade spheno-orbital meningioma in patients with systemic lupus erythematosus: Two case reports and literature review.

Authors:  Sarah Bin Abdulqader; Nasser Almujaiwel; Wafa Alshakweer; Gmaan Alzhrani
Journal:  Surg Neurol Int       Date:  2020-10-29
  6 in total

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