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Case Reports
. 2024 Oct 6;16(10):e70950.
doi: 10.7759/cureus.70950. eCollection 2024 Oct.

Giant Chondromyxoid Fibroma Associated With Epileptic Seizures: A Case Report

Affiliations
Case Reports

Giant Chondromyxoid Fibroma Associated With Epileptic Seizures: A Case Report

Corneliu Toader et al. Cureus. .

Abstract

This case report presents an exceedingly rare instance of skull base chondromyxoid fibroma (CMF) managed surgically. Chondromyxoid fibromas are very rare tumors (<1% of benign bone tumors), the occurrence in the skull area being even more rare. The location of tumors at the skull base makes their surgical resection extremely challenging, usually resulting in subtotal resection (STR). One aspect that makes this case stand out is its unique clinical presentation, particularly the presence of epileptic seizures. Patients suffering from skull base CMFs must receive regular follow-up exams in order to track disease progress, maintain quality of life, and prevent further complications.

Keywords: chondromyxoid fibroma; epileptic seizures; neurosurgery; skull base; subtotal resection.

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Conflict of interest statement

Human subjects: Consent was obtained or waived by all participants in this study. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

Figures

Figure 1
Figure 1. Sagittal section of the MRI examination
The MRI shows a voluminous, expansive, multilobulated process in the right temporal lobe with an infratentorial component that engulfs both the middle cerebral artery and the apex of the basilar artery.
Figure 2
Figure 2. Transverse section of the MRI
An infiltrative component is observed in the right half of the clivus, the right half of the sella turcica, and the cavernous sinus.
Figure 3
Figure 3. (A) Lobules have stellate cells in a myxoid background and reside in lacunae in chondroid areas (H&E 10X); (B) Lobules have stellate cells in a myxoid background and reside in lacunae in chondroid areas (H&E 40x); (C) Myxoid to chondroid stroma, representing various stages of cartilaginous development (H&E 20x); (D) Paucicellular chondroid proliferation consisting of relatively monomorphic chondrocytic type cells mixed with fibroblastic type cells with a stellate or spindle shape appearance (H&E 40x); (E) Slightly lobular chondroid tumor formation showing on the periphery a fragment of sclerotic bone tissue and skeletal muscle fibers (H&E 4x); (F) Come chondroid areas are sequestered in compact bone tissue with areas of osteosclerosis (H&E 4x)
Figure 4
Figure 4. Surgical resection of the tumor
Sub-total resection of the tumoral mass
Figure 5
Figure 5. MRI with contrast showed a minimal area of tumor recurrence in the right basal frontotemporal region, without mass effect or indication for surgery.
Figure 6
Figure 6. A cranial CT scan, both native and with contrast, demonstrated minimal area of tumor recurrence in the right basal frontotemporal region, without mass effect or surgical indication.

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