Authors :
Dr. Komal S. Godase; Dr. Uday S. Mohite; Dr. Vivek S. Gosavi; Dr. Mayur Kulkarni
Volume/Issue :
Volume 9 - 2024, Issue 5 - May
Google Scholar :
https://tinyurl.com/4h2watxu
Scribd :
https://tinyurl.com/4hdp7wss
DOI :
https://doi.org/10.38124/ijisrt/IJISRT24MAY691
Note : A published paper may take 4-5 working days from the publication date to appear in PlumX Metrics, Semantic Scholar, and ResearchGate.
Abstract :
Purpose
To describe a presentation of Foster Kennedy
syndrome (FKS) with a distinct pattern: one eye shows
optic nerve atrophy due to compression by an
intracranial tumor, while the other eye exhibits optic disc
edema caused by heightened intracranial pressure. This
atypical presentation highlights how commonplace
clinical signs can mask a rare condition or disease
phenotype.
Case Report
A 26-year-old woman visited an ophthalmologist
reporting sudden vision loss in her left eye over the past
two months, accompanied by untreated headaches. She
had no other health concerns. Her best corrected visual
acuity was 6/36p in the right eye and PL+PR Faulty in the
left eye. A relative afferent pupillary defect of grade 2 was
observed in the left eye. Intraocular pressures were
normal. Extra ocular movements were normal. Fundus
examination revealed optic atrophy in left eye and frank
optic disc edema in right eye. MRI brain scan was advised
to patient to look for space occupying lesions. MRI
imaging showed a 3.1x3.4x3.8cm sized predominantly
cystic lesion involving sella and supra-sellar region
appearing hyper intense on both T2/FLAIR and T1 with
peripheral blooming and peripheral enhancement of solid
component with extensions s/o adamantinomatous
Craniopharyngioma with Superiorly-compression and
elevation of optic chiasma, bilateral optic tracts. And
hence patient is diagnosed as case of Foster Kennedy
syndrome. The patient was given Nepafenac 0.1% eye
drop once daily for two weeks. The patient was referred
for a neurosurgical consultation and Craniotomy with
aspiration was done by neurosurgeon and sample is sent
for cytology.
Conclusion
When encountering a patient with optic atrophy in
one eye along with optic disc edema in the other eye,
suspicion should arise regarding the presence of a space-
occupying lesion. A concise case history , extensive ocular
work up and cranial magnetic resonance imaging
showing sudden visual loss and raised intracranial
pressure which give rise to the diagnosis of sight
threatening, permanent and fatal condition such as Foster
Kennedy Syndrome.
Keywords :
Foster Kennedy Syndrome (FKS), Vision Loss, Optic Atrophy, Intracranial Hypertension.
References :
- Hata M, Miyamoto K. Causes and Prognosis of Unilateral and Bilateral Optic Disc Swelling. Neuroophthalmology. 2017 Aug;41(4):187-191.
- Eidet JR, Biernat D, Dahlberg D, Wiedmann MKH, Jørstad ØK. [Foster Kennedy Syndrome]. Tidsskr Nor Laegeforen. 2019 Jun 25;139(10) 3. Zehden J,
- Harish Bindiganavile S, Bhat N, Lee AG. Compressive Optic Disc Edema and Contralateral Papilledema: Type 2 Foster Kennedy Variant Syndrome. J Neuroophthalmol. 2021 Jun 01;41(2):e217-e219
- Ogasawara C, Philbrick BD, Adamson DC. Meningioma: A Review of Epidemiology, Pathology, Diagnosis, Treatment, and Future Directions. Biomedicines. 2021 Mar 21;9(3)
- Hang J, Sai K, Zhu ZQ, Lin FH, Wang ZF, Chen YM, Huang CY, Ye YL, Wang XL, Li YP, Sun SX, Zhong WY, Chen JB, Yang YQ. Prognostic factors for olfactory groove meningioma with nasal cavity extension. Oncotarget. 2018 Jan 12;9(4):4607-4613.
- Sun C, Dou Z, Wu J, Jiang B, Iranmanesh Y, Yu X, Li J, Zhou H, Zhong C, Peng Y, Zhuang J, Yu Q, Wu X, Yan F, Xie Q, Chen G. The Preferred Locations of Meningioma According to Different Biological Characteristics Based on Voxel-Wise Analysis. Front Oncol. 2020;10:1412.
- Ostrom QT, Cioffi G, Gittleman H, Patil N, Waite K, Kruchko C, Barnholtz-Sloan JS. CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2012-2016. Neuro Oncol. 2019 Nov 01;21(Suppl 5):v1-v100.
- Berry, S.; Lin, W.V.; Sadaka, A.; Lee, A.G. Nonarteritic anterior ischemic optic neuropathy: Cause, effect, and management. Eye Brain 2017, 9, 23–28.
- Hamard, H.; Desbordes, J.M. Pathologie iatrogène du nerf optique (Iatrogenic pathology of the optic nerve). L’Annee Ther. Clin. Ophtalmol. 1982, 33, 185–202.
- Pinazo-Duran, M.D.; Renau-Piqueras, J.; Guerri, C.; Strömland, K. Optic Nerve Hypoplasia in Fetal Alcohol Syndrome: An Update. Eur. J. Ophthalmol. 1997, 7, 262–270.
- Shams, P.N.; Plant, G.T. Optic neuritis: A review. Int. MS J. 2009, 16, 82–89.
- Musa, M.; Aluyi-Osa, G.; Zeppieri, M. Foster Kennedy Syndrome (FKS): A Case Report. Clin. Pract. 2022, 12, 527–532.
Purpose
To describe a presentation of Foster Kennedy
syndrome (FKS) with a distinct pattern: one eye shows
optic nerve atrophy due to compression by an
intracranial tumor, while the other eye exhibits optic disc
edema caused by heightened intracranial pressure. This
atypical presentation highlights how commonplace
clinical signs can mask a rare condition or disease
phenotype.
Case Report
A 26-year-old woman visited an ophthalmologist
reporting sudden vision loss in her left eye over the past
two months, accompanied by untreated headaches. She
had no other health concerns. Her best corrected visual
acuity was 6/36p in the right eye and PL+PR Faulty in the
left eye. A relative afferent pupillary defect of grade 2 was
observed in the left eye. Intraocular pressures were
normal. Extra ocular movements were normal. Fundus
examination revealed optic atrophy in left eye and frank
optic disc edema in right eye. MRI brain scan was advised
to patient to look for space occupying lesions. MRI
imaging showed a 3.1x3.4x3.8cm sized predominantly
cystic lesion involving sella and supra-sellar region
appearing hyper intense on both T2/FLAIR and T1 with
peripheral blooming and peripheral enhancement of solid
component with extensions s/o adamantinomatous
Craniopharyngioma with Superiorly-compression and
elevation of optic chiasma, bilateral optic tracts. And
hence patient is diagnosed as case of Foster Kennedy
syndrome. The patient was given Nepafenac 0.1% eye
drop once daily for two weeks. The patient was referred
for a neurosurgical consultation and Craniotomy with
aspiration was done by neurosurgeon and sample is sent
for cytology.
Conclusion
When encountering a patient with optic atrophy in
one eye along with optic disc edema in the other eye,
suspicion should arise regarding the presence of a space-
occupying lesion. A concise case history , extensive ocular
work up and cranial magnetic resonance imaging
showing sudden visual loss and raised intracranial
pressure which give rise to the diagnosis of sight
threatening, permanent and fatal condition such as Foster
Kennedy Syndrome.
Keywords :
Foster Kennedy Syndrome (FKS), Vision Loss, Optic Atrophy, Intracranial Hypertension.