[Frontal chondroma of the falx cerebri].

Rev Clin Esp

Published: November 1953

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Article Synopsis
  • This study focuses on analyzing the CT and MR imaging characteristics of intracranial extra-axial chondromas in six patients, highlighting their distinct appearances based on location.
  • The researchers found that frontal chondromas typically showed calcification and mixed signals on imaging, while cavernous sinus chondromas displayed bone erosion and intense hyperintensity on T2-weighted images without calcification.
  • The study concludes that while there are various imaging features, specific traits like absence of restricted diffusion and distinct signal patterns can suggest the presence of an intracranial chondroma, aiding in diagnosis.
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Background: Intracranial chondromas account for 0.2-0.3% of all intracranial neoplastic lesions and less than a quarter arise in the convexity or falx.

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An Intracerebral Type of Cranial Chondroma.

Brain Tumor Res Treat

April 2020

Department of Neurosurgery, Dongsan Hospital, Keimyung University School of Medicine, Daegu, Korea.

The vast majority of intracranial chondromas are located in the base of the cranium. Their presentation as an intracerebral neoplasm is considered to be extremely rare. A previously healthy 45-year-old man experienced recurrent seizure attacks over a period of 6 months.

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BACKGROUND Intracranial chondroma is a rare benign tumor that more commonly arises from the skull base. Chondroma arising from the falx cerebri is very rare, with only 19 cases previously reported in the literature. The imaging characteristics of intracranial chondroma and meningioma can be similar.

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Distinguishing Falcine Chondrosarcomas from Their Mimics and Management.

World Neurosurg

October 2018

Departments of Neurosurgery, National Institute of Neurology Tunis, Tunisia Faculty of Medicine, University of Tunis El Manar, Tunis, Tunisia.

Background: Primary intracranial chondrosarcoma is an extremely rare malignant tumor of the central nervous system, which accounts for <0.16% of all primary intracranial tumors. This rare tumor has a high associated morbidity from the tumor itself as well as from treatment modalities.

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