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Meningioma subtypes classification is a real-world multiclass problem from the realm of neuropathology. The major challenge in solving this problem is the inherent complexity due to high intra-class variability and low inter-class variation in tissue samples. The development of computational methods to assist pathologists in characterization of these tissue samples would have great diagnostic and prognostic value. In this article, we proposed an optimized evolutionary framework for the classification of benign meningioma into four subtypes. This framework investigates the imperative role of RGB color channels for discrimination of tumor subtypes and compute structural, statistical and spectral phenotypes. An evolutionary technique, Genetic Algorithm, in combination with Support Vector Machine is applied to tune classifier parameters and to select the best possible combination of extracted phenotypes that improved the classification accuracy (94.88%) on meningioma histology dataset, provided by the Institute of Neuropathology, Bielefeld. These statistics show that computational framework can robustly discriminate four subtypes of benign meningioma and may aid pathologists in the diagnosis and classification of these lesions.
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http://dx.doi.org/10.1002/jemt.22874 | DOI Listing |
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 PDFDiagn Cytopathol
September 2025
Department of Pathology, University of Health Science, Istanbul Training and Research Hospital, Istanbul, Turkey.
This case report presents the cytological characteristics of an extracranial anaplastic meningioma-an exceptionally rare entity rarely sampled via fine-needle aspiration. We aim to highlight specific cytomorphological features that may aid in the preoperative identification of the anaplastic subtype.
View Article and Find Full Text PDFCureus
July 2025
Radiation Oncology, Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, MAR.
While meningiomas are the most frequent among adult primary intracranial tumors, they remain a rare condition in children, accounting for less than 5% of pediatric central nervous system tumors. These tumors have been linked to conditions like neurofibromatosis type 2 and radiation exposure, and they usually present with increased intracranial pressure and other neurological symptoms. Diagnosis relies on magnetic resonance imaging (MRI), which reveals heterogeneous masses often mistaken for other types of tumors.
View Article and Find Full Text PDFInt J Surg Case Rep
August 2025
Department of Medicine, An Najah National University, Nablus, Palestine.
Introduction And Importance: Meningiomas are the most common primary tumors of the central nervous system. Atypical meningiomas, classified as World Health Organization (WHO) grade II, are relatively rare, accounting for 5-7 % of cases, and are known for their aggressive behaviour, including higher recurrence rates and potential brain invasion. Early detection and intervention are crucial, even in asymptomatic patients.
View Article and Find Full Text PDFNo Shinkei Geka
July 2025
Department of Neurosurgery, the University of Tokyo.
Neurofibromatosis type 2 (NF2), now redefined as NF2-related schwannomatosis (NF2-SWN), is a hereditary tumor syndrome characterized by bilateral vestibular schwannomas, multiple meningiomas, and other central nervous system tumors. The revised diagnostic criteria incorporate genetic testing and consideration of somatic mosaicism, enabling a more accurate and earlier diagnosis. A strong genotype-phenotype correlation has been established: truncating mutations are associated with an earlier onset and severe clinical course, whereas missense or splice-site mutations are often linked to milder phenotypes and better functional outcomes.
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