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Background: Inflammatory pseudotumor is non-neoplastic lesions that form tumor-like masses, typically occurring in the lungs and orbits, with rare involvement of intracranial regions such as the Meckel cave. While neuroimaging can assist in differential diagnosis, definitive diagnosis may remain challenging. Some cases are associated with immunoglobulin G4 (IgG4)-related disease, highlighting the importance of histopathological confirmation to guide appropriate management.
Case Description: A case of a 42-year-old woman presented with facial numbness and headache. Magnetic resonance imaging revealed a 25-mm enhancing mass in the left Meckel cave, initially suspected to be a trigeminal schwannoma. Craniotomy and tumor resection were performed. Intraoperative findings and rapid pathology indicated marked inflammatory cell infiltration without features of schwannoma. The final diagnosis was inflammatory pseudotumor, with no evidence of IgG4-related disease or malignancy. Postoperative symptoms improved, and only a short course of steroids was administered.
Conclusion: This case underscores the diagnostic difficulty of distinguishing inflammatory pseudotumor from neoplastic lesions in skull base regions. Surgical biopsy or resection is critical for definitive diagnosis, especially in cases with progressive symptoms. Individualized treatment planning based on disease activity and neurological impact remains essential due to the absence of standardized treatment guidelines.
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http://dx.doi.org/10.25259/SNI_447_2025 | DOI Listing |
Neurosurg Focus
September 2025
Objective: The therapy of choice for classical trigeminal neuralgia (TN) is usually microvascular decompression (MVD). Although in most surgical procedures the view with the operating microscope is sufficient to inspect the entire course of the trigeminal nerve from the brainstem to Meckel's cave, anatomical abnormalities may hinder the view. In these conditions, visualization with an endoscope with an angulated view provides additional exposure and may identify a compression that was hidden on microscopic view.
View Article and Find Full Text PDFReports (MDPI)
August 2025
Department of ENT, Medical University of Sofia, 1431 Sofia, Bulgaria.
: Petrous bone cholesteatoma is a rare and complex condition that poses significant challenges in terms of its diagnosis and treatment. This benign yet locally aggressive lesion can cause extensive destruction of the surrounding structures, potentially leading to serious complications. : We present a case of extensive petrous bone cholesteatoma involving nearly the entire skull base.
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, Interzonal General Acute Hospital Petrona V. de Cordero, Ministry of Health, San Fernando, Argentina.
Background: An enlarged suprameatal tubercle (EST) has been described as an uncommon anatomical variant that may be encountered during cerebellopontine angle surgery. It can limit exposure during microvascular decompression (MVD) of the trigeminal nerve, particularly when the neurovascular conflict is located distal to the root entry zone (REZ), potentially posing a surgical challenge.
Case Description: We present the case of a 66-year-old woman with a history of medically refractory left-sided V2-V3 typical trigeminal neuralgia, previously treated with radiofrequency ablation without clinical improvement.
Surg Neurol Int
July 2025
Department of Neurosurgery, Ohnishi Neurological Center, Akashi, Hyogo, Japan.
Background: Inflammatory pseudotumor is non-neoplastic lesions that form tumor-like masses, typically occurring in the lungs and orbits, with rare involvement of intracranial regions such as the Meckel cave. While neuroimaging can assist in differential diagnosis, definitive diagnosis may remain challenging. Some cases are associated with immunoglobulin G4 (IgG4)-related disease, highlighting the importance of histopathological confirmation to guide appropriate management.
View Article and Find Full Text PDF