Progressive Double Arcuate Scotoma is a Rare Presentation in Falx Meningioma Cerebri

Authors

  • Zainal Abidin Mohd-Khairy Universiti Sains Malaysia
  • Wan Hitam Wan-Hazabbah Universiti Sains Malaysia

Keywords:

falx meningioma, glaucoma suspect, visual field defect, arcuate scotoma

Abstract

A 77-year-old woman with multiple comorbidities, who is a glaucoma suspect, presented with a progression of a double arcuate visual filed defect over a five-month period. The intraocular pressure was within normal limit, and the cup-to-disc ratio was between 0.6 to 0.7 in both eyes. A computed tomography (CT) scan of the brain revealed a large, well-circumsribed hyperdense mass in the right occipital lobe, with heterogenous enhancement post-contrast and obliteration of the third ventricle. Magnetic resonance imaging (MRI) showed a well-defined, extra-axial, rounded mass in the right parieto-occipital region, with a cerebrospinal fluid cleft, a dural tail sign and broad base consistent with a right parieto-occipital falx meningioma. The patient was advised to undergo surgical removal of the mass; however, she declined due to her advanced age and the absence of neurological abnormalities, except for the visual field defect. In conclusion, a high index of suspicion is warranted in patients who are glaucoma suspects and present with progressive visual field defects. A progressive double arcuate visual field defect may indicate an underlying silent occipital pathology.

Author Biographies

  • Zainal Abidin Mohd-Khairy, Universiti Sains Malaysia
    Department of Ophthalmology & Visual Science
  • Wan Hitam Wan-Hazabbah, Universiti Sains Malaysia
    Department of Ophthalmology & Visual Science

References

References

Chung SB, Kim CY, Park CK, Kim DG, Jung HW. Falx meningiomas: surgical results and lessons learned from 68 cases. J Korean Neurosurgical Soc. 2007:42(4):276-280. doi: 10.3340/jkns.2007.42.4.276.

Kedar S, Ghate D, Corbet JJ. Visual field in neuro-ophthalmology. Indian J Ophthalmol. 2011:59(2), 103-109. doi: 10.4103/0301-4738.77013.

Ostrom QT, Cioffi G, Gittleman H, Patil N, Waite K, Kruchko C, et al. CBTRUS statistical report: primary brain and other central nervous system tumors diagnosed in the United States in 2012–2016. Neuro Oncol. 2019;21(Suppl 5):v1-v100. doi: 10.1093/neuonc/noz150.

Watts J, Box G, Galvin A, Brotchie P, Trost N, Sutherland T. Magnetic resonance imaging of meningiomas: a pictorial review. Insights Imaging. 2014;5(1):113–122. doi: 10.1007/s13244-013-0302-4.

Buetow MP, Buetow PC, Smirniotopoulos JG. Typical, atypical, and misleading features in meningioma. Radiographics. 1991;11(6):1087–1106. doi: 10.1148/radiographics.11.6.1749851.

Heiss WD, Raab P, Lanfermann H. Multimodality assessment of brain tumors and tumor recurrence. J Nucl Med. 2011;52(10): 1585-1600. doi: 10.2967/jnumed.110.084210.

Goldbrunner R, Minniti G, Preusser M, Jenkinson MD, Sallabanda K, Houdart E, et al. EANO guidelines for the diagnosis and treatment of meningiomas. Lancet Oncol. 2016;17(9): e383-9. doi: 10.1016/S1470-2045(16)30321-7.

Maggio I, Franceschi E, Tosoni A, Nunno VD, Gatto L, Lodi R, Brandes AA. Meningioma: not always a benign tumor. A review of advances in the treatment of meningiomas. CNS Oncol. 2021;10(2):CNS72. doi: 10.2217/cns-2021-0003.

Karsy M, Guan J, Cohen A, Colman H, Jensen RL. Medical management of meningiomas: current status, failed treatments, and promising horizons. Neurosurg Clin N Am. 2016;27(2): 249-260. doi: 10.1016/j.nec.2015.11.002.

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Published

2025-08-04

Issue

Section

Journal of Biomedical and Clinical Sciences