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The vast majority of chondrosarcomas of the skull (CS) are located at the skull base and represent locally aggressive malignant tumors that account for 0.15% of all intracranial neoplasms. Complete surgical resection with wide surgical margins is currently the main treatment strategy, but can be hard to achieve due to the complex anatomy of the head and neck. The jugular foramen, situated in the floor of the posterior fossa and posterolaterally to the petro-occipital suture, is a remarkably rare location for CS. A case of primary CS of the jugular foramen in a 65-year-old patient is reported, presenting with otalgia, pulsatile tinnitus, and mild hearing loss in the left ear, accompanied by peripheral facial nerve paresis. Radiographic imaging showed a mass in the left mastoid, middle ear and jugular fossa with bone destruction of the jugular fossa and mastoid, while magnetic resonance imaging showed additional involvement of the petroclival fissure, hypoglossal canal, jugular bulb, and sigmoid sinus. The tumor was resected with wide margins through a Fisch infratemporal fossa approach type A, followed by radiotherapy. Results of the immunophenotyping along with histological features primarily matched moderately differentiated chondrosarcoma. The patient is recurrence free at 6 months after treatment. Middle ear discharge with facial palsy as a first manifestation of the CS has not been described to date. The unique localization, treatment details and histopathologic data are relevant in expanding the current level of knowledge on the subject.
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http://dx.doi.org/10.5152/iao.2025.231362 | DOI Listing |
Introduction: Cochlear implantation (CI) may be used as a viable method for restoring hearing in patients with sensorineural hearing loss (SNHL) caused by jugular foramen tumors.
Materials And Methods: 42-year-old female presenting with sudden-onset SNHL, pulsatile tinnitus, and otalgia, with a PTA of 119 dB and AzBio sentence score of 0% in quiet. Brain MRI identified a 22 mm tumor within the left jugular foramen and hypoglossal canal involving the cochlear aqueduct.
J Neurosurg Case Lessons
August 2025
Department of Neurosurgery, Kurashiki Central Hospital, Kurashiki, Japan.
Background: In dural arteriovenous fistulas, bridging veins are connecting vessels that drain venous blood from the surface of the brain to the surrounding dural sinus. It is rare for the fistulous point and the bridging vein to be at different levels.
Observations: A 71-year-old man presented with progressive spinal symptoms of 8 months' duration.
No Shinkei Geka
July 2025
Department of Neurosurgery, Tominaga Hospital.
Stereotactic radiation therapy, including stereotactic radiosurgery, is a well-established and effective treatment for cerebellopontine angle tumors such as meningiomas, vestibular schwannomas, trigeminal and jugular foramen schwannomas, and glomus tumors. It offers high rates of tumor control while preserving neurological function, particularly in tumors smaller than 3 cm, which are ideal candidates for stereotactic radiosurgery. Large tumors or those extending beyond the skull base can also be managed effectively using fractionated stereotactic radiation therapy.
View Article and Find Full Text PDFNo Shinkei Geka
July 2025
Department of Neurosurgery, Osaka Medical and Pharmaceutical University.
Jugular foramen schwannoma is a rare intracranial tumor, with few opportunities for surgeons to perform tumor excision. This study aimed to provide an outline of jugular foramen schwannoma and our surgical strategy for this tumor. The surgical approach depends on tumor growth patterns with or without extracranial extension.
View Article and Find Full Text PDFNo Shinkei Geka
July 2025
Department of Radiology, Kyorin University Faculty of Medicine.
MRI is the most effective imaging tool for diagnosing cerebellopontine angle tumors, although CT is also useful for evaluating bone changes and detecting calcification. Regarding MRI, it is recommended to efficiently use MR cisternography, a small imaging field of view, and a thin slice thickness. The most common tumor type is acoustic schwannoma, followed by meningioma, trigeminal, facial nerve, jugular foramen schwannoma, paraganglioma, and others.
View Article and Find Full Text PDF