Primary Extraskeletal Falcine Myxoid Chondrosarcoma—A Case Report and Review of Literature

Author:

Narayanan Rajasekhar1,Venugopal Renjith T.1,L. Suresh Kumar K.1,B. Jose P.1,Bahuleyan Anjana2,P. Reshmi C.3,Varghese Thomas1,Pillai Marthanda A.1

Affiliation:

1. Department of Neurosurgery, Ananthapuri Hospitals and Research Institute, Thiruvananthapuram, Kerala, India

2. Department of Pathology, Ananthapuri Hospitals and Research Institute, Thiruvananthapuram, Kerala, India

3. Department of Radiodiagnosis, Ananthapuri Hospitals and Research Institute, Thiruvananthapuram, Kerala, India

Abstract

AbstractIntracranial chondrosarcomas are rare malignant lesions. Both skull base and dural-based extraosseous chondrosarcomas have been reported to occur intracranially. Dural-based chondrosarcomas arising from the falx cerebri are rare lesions with only 19 cases reported till date. Although conventional, mesenchymal, and myxoid variants of chondrosarcomas have been reported intracranially, myxoid variant are the rarest with only 17 cases reported till date, among which only 2 were falcine. We are reporting the third case of falcine myxoid chondrosarcoma in a 32-year-old man who presented with seizures and subtle lower limb weakness. Radiological findings were suggestive of an atypical meningioma in the falcine region. Macroscopically total resection of the tumor was done. Histopathological examination confirmed myxoid chondrosarcoma, grade 1. Postoperative period was uneventful, and the patient remains asymptomatic 34 months after the surgery without the application of any adjuvant therapy. Falcine myxoid chondrosarcomas are extremely rare lesions with variable aggressiveness as suggested by the three cases reported till now including the present case.

Publisher

Georg Thieme Verlag KG

Reference24 articles.

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