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Tolosa-Hunt syndrome (THS) is a rare idiopathic granulomatous inflammation of the cavernous sinus, superior orbital fissure, or orbital apex, presenting with painful ophthalmoplegia. The exact etiology remains unclear, but it is believed to be immune-mediated. Early diagnosis is essential, as prompt corticosteroid therapy results in rapid symptom resolution. This case report highlights the clinical presentation, diagnostic workup, and management of a patient with Tolosa-Hunt syndrome, emphasizing the role of neuroimaging in confirming the diagnosis and the efficacy of corticosteroid treatment. A 55-year-old male presented with a persistent right-sided headache for 2.5 months, accompanied by diplopia for 5 days. Neurological and ophthalmic examination revealed right-sided ptosis, restricted extraocular movements, and binocular diplopia. MRI findings demonstrated an asymmetric enlargement of the right cavernous sinus with inflammatory changes extending into the orbital apex and superior orbital fissure, confirming Tolosa-Hunt syndrome. The patient was treated with high-dose corticosteroids, leading to significant clinical improvement. Following corticosteroid therapy, the patient experienced rapid resolution of headache and improvement in ocular motility. Repeat MRI after 6 weeks showed a marked reduction in inflammation. There was no recurrence of symptoms upon gradual steroid tapering. Tolosa-Hunt syndrome should be considered in patients with unilateral headache and painful ophthalmoplegia. MRI plays a crucial role in diagnosis, and corticosteroids remain the mainstay of treatment, leading to excellent outcomes. Early recognition and intervention can prevent long-term complications and disability.
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http://dx.doi.org/10.1016/j.radcr.2025.03.084 | DOI Listing |
Front Neurol
July 2025
Department of Neurology, Beijing Chaoyang Hospital, Capital Medical University, Beijing, China.
Objective: Investigating the clinical features and etiological diagnosis of early isolated ocular motor nerve palsy to deepen understanding of the condition.
Methods: We retrospectively enrolled 68 patients with isolated ocular motor nerve palsy admitted our hospital between 2017 and 2024. A retrospective analysis was conducted to assess their clinical and imaging characteristics.
Int J Surg Case Rep
August 2025
Department of Radiology, B and B hospital, Gwarko, Lalitpur, Nepal.
Introduction And Importance: There exist some potential complications following chiari decompression surgery but tolosa hunt syndrome(THS) as a possible complication has never been reported in medical literature. Despite considered as a diagnosis of exclusion, tolosa hunt syndrome as late complication following posterior fossa decompression surgery for chiari 1 malformation is a potential differential.
Case Summary: 20 years old male presented with headache and multiple ocular complaints 36 day after posterior fossa decompression surgery for Chiari I malformation.
Cureus
May 2025
Radiology, Dammam Medical Complex, Dammam, SAU.
Tolosa-Hunt syndrome (THS) is a rare neurological condition characterized by ophthalmoplegia preceded by retroorbital pain or headache. It mainly involves cranial nerves III, IV, and VI. The majority of the time, the cause is unknown; it is believed that the cause is nonspecific granulomatous inflammation of the cavernous sinus and superior orbital fissure or rarely beyond.
View Article and Find Full Text PDFNeurol Sci
September 2025
Department of Internal Medicine, Neurology Unit, Security Forces Hospital Makkah, Makkah, Kingdom of Saudi Arabia.
Background: Tolosa-Hunt Syndrome (THS) is a rare inflammatory condition characterized by painful ophthalmoplegia, often associated with granulomatous inflammation in the cavernous sinus. While typically idiopathic, THS can sometimes be linked to underlying autoimmune diseases. This report presents the first documented case of THS as the initial manifestation of Sjögren's Syndrome (SS).
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