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Calcifying pseudoneoplasms of the neuraxis (CAPNON) are rare non-neoplastic calcified lesions that can occur throughout the entire neuraxis. Cranial nerves may be involved in skull base lesions. Surgical resection usually has a good prognosis, with only a few cases of recurrence reported in the relevant literature. We experienced a recurrent case of CAPNON in Meckel's cave extending to the cerebellopontine cistern with involvement of the trigeminal nerve after initial resection of the cystic part of the lesion. A 48-year-old man presented with a 4-year history of right-sided ptosis. Magnetic resonance imaging revealed a calcified lesion arising in Meckel's cave, with a cystic lesion extending to the cerebellopontine cistern. The cystic part of the lesion was excised during the initial surgery using the right lateral suboccipital approach. However, the cystic lesion regrew to its preoperative size within 23 months. The right extradural subtemporal approach was used to successfully remove both the calcified mass in the right Meckel cave and the cystic lesion extending to the right cerebellopontine cistern during the resection of the lesion. The patient's neurological symptoms resolved postoperatively. CAPNON was identified during the histopathological examination. This report describes a rare case of CAPNON in Meckel's cave with a unique clinical course. After the first operation, cystic lesions recurred in the cerebellopontine cistern, but they were successfully treated by a second operation.
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http://dx.doi.org/10.1055/s-0045-1806859 | DOI Listing |
NMC Case Rep J
August 2025
Department of Neurosurgery, Osaka Neurological Institute, Toyonaka, Osaka, Japan.
Dural arteriovenous fistula can present with cerebral venous sinus thrombosis and retrograde leptomeningeal venous drainage. Given the associated intracranial hemorrhage risk, immediate retrograde leptomeningeal venous drainage obliteration is desirable. Herein, we report a case of dural arteriovenous fistula with acute cerebral venous sinus thrombosis and intracranial hemorrhage that was successfully managed using sinus thrombectomy alone.
View Article and Find Full Text PDFAsian J Neurosurg
September 2025
Department of Neurosurgery, Asahi University Hospital, Gifu, Japan.
Calcifying pseudoneoplasms of the neuraxis (CAPNON) are rare non-neoplastic calcified lesions that can occur throughout the entire neuraxis. Cranial nerves may be involved in skull base lesions. Surgical resection usually has a good prognosis, with only a few cases of recurrence reported in the relevant literature.
View Article and Find Full Text PDFSurg Neurol Int
July 2025
Department of Neurosurgery, Hospital Padilla de Tucuman, Tucuman, Argentina.
Background: Choroid plexus papillomas of the infratentorial compartment are rare, benign tumors, commonly arising from the inferior roof of the fourth ventricle, with frequent extension into the foramina of Magendie and Luschka and toward the cerebellopontine cistern. Clinical presentation often reflects intracranial hypertension due to cerebrospinal fluid obstruction and, occasionally, hypersecretion. Neurological deficits may include cranial nerve palsies, cerebellar signs, and altered mental status secondary to brainstem and cerebellar compression.
View Article and Find Full Text PDFSurg Neurol Int
July 2025
Department of Neurological Surgery Urayasu, Chiba, Japan.
Background: Hemifacial spasms are involuntary paroxysmal muscle contractions commonly presenting as unilateral involvement of the orbicularis oculi and oris muscles.
Case Description: A 62-year-old woman presented with spasms of progressively increasing frequency for 2 months in the right orbicularis oculi muscle, with subsequent involvement of the orbicularis oris muscle. Cerebral magnetic resonance imaging revealed an intensely enhanced dural-based tumor in the right posterior fossa.
World Neurosurg
June 2025
Department of Neurosurgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA; Semmes Murphey Clinic, Memphis, Tennessee, USA. Electronic address:
Intracranial epidermoid cysts are rare, benign lesions accounting for 1% of intracranial tumors. They may arise from misplaced squamous epithelium during neural tube closure, and are found in the paramedian position, cerebellopontine angle, or parasellar region with other locations considered rare. The far lateral approach and its extensions enables access and visualization of ventral and ventrolateral lesions at the craniocervical junction without retraction.
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