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Blepharospasm, characterized by abnormal blinking and sensory hypersensitivity such as photophobia and ocular pain, is thought to arise from pathological sensorimotor integration. We report a rare case of a male teenager with a growth hormone-secreting giant pituitary adenoma compressing both the optic chiasm and bilateral trigeminal nerves. Initially, the patient presented with visual disturbances and bitemporal hemianopia, without photophobia or ocular pain. Following partial tumor resection, which relieved compression of the optic chiasm but not the trigeminal nerves, he developed severe photophobia, deep ocular pain, and bilateral secondary blepharospasm. These symptoms persisted despite pharmacologic interventions, including pregabalin and topical rebamipide. A second surgery, which decompressed the trigeminal nerves, led to the complete resolution of all symptoms. The clinical course suggests that trigeminal nerve compression, particularly of the ophthalmic branch (V1), may induce hypersensitivity states resulting in neuropathic pain, photophobia, and secondary blepharospasm. We hypothesize that initial optic chiasm compression suppressed photophobia by disrupting non-visual photophobia circuits through the suprachiasmatic nuclei to pulvinar nuclei. After decompression, restoration of this pathway unmasked the hypersensitivity induced by ongoing trigeminal compression. The complete resolution of symptoms following trigeminal decompression supports the role of peripheral sensory nerve compression in the pathogenesis of photophobia and secondary blepharospasm. This case provides novel clinical evidence for the interrelationship between the trigeminal and visual pathways in sensorimotor disorders.
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http://dx.doi.org/10.7759/cureus.91148 | DOI Listing |
Pract Neurol
September 2025
Neurology Department, Croydon University Hospital, London, England, UK
A 22-year-old woman had an 8-year history of progressive bilateral vision loss and of diabetes mellitus. Her mother had diabetes and two first cousins had severe congenital deafness. On examination, her visual acuities were 6/36 bilaterally, with absent colour vision and gross optic disc pallor.
View Article and Find Full Text PDFJ Neurooncol
September 2025
Department of Radiation Oncology, Massachusetts General Hospital, Boston, USA.
Purpose: Cranial irradiation is associated with health-related quality of life (HRQoL) deficits in childhood cancer survivors. We investigated the relationship between radiation dose to brain substructures and HRQoL in children with brain tumors treated with proton beam therapy (PBT).
Methods: Data were obtained from children in the Pediatric Proton/Photon Consortium Registry who received PBT for primary brain tumors between 2015 and 2021.
J Neurosurg Case Lessons
September 2025
Department of Neurosurgery, Kantonsspital Aarau, Switzerland.
Background: Meningioma en plaque (MEP) is a rare subtype of meningioma with a carpet-like growth pattern, often causing hyperostosis. Even rarer is the presentation of bilateral MEP posing diagnostic and therapeutic challenges. Management of MEP usually entails early complete resection.
View Article and Find Full Text PDFNeurol Neurochir Pol
September 2025
Institute of Medical Sciences, Collegium Medicum, University of Zielona Góra, Zielona Góra, Poland.
Front Psychiatry
August 2025
Department of Child and Adolescent Psychiatry, Faculty of Medicine Hospital, Necmettin Erbakan University, Konya, Türkiye.
Introduction: The aim of this study is to investigate, using magnetic resonance imaging (MRI), the optic nerve diameter, morphometric characteristics of the optic chiasm (OC), volumes of the lateral, third, and fourth ventricles, as well as the volumes of the corpus callosum (CC) and choroid plexus (CP) in children with autism spectrum disorder (ASD), and to compare these findings with those of a typically developing (TD) control group. Additionally, the study seeks to evaluate the impact of these neuroanatomical parameters on autism symptom severity and sensory sensitivity.
Methods: This study included 111 children with ASD and 143 TD control children, aged between 5 and 13 years.