open access

Vol 48, No 4 (2014)
Case reports
Submitted: 2014-02-22
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A rare tentorial mesenchymal chondrosarcoma in posterior cranial fossa: Case report

Anqi Xiao1, Zhenlin Li2, Xin He3, Chao You1
DOI: 10.1016/j.pjnns.2014.06.001
·
Neurol Neurochir Pol 2014;48(4):287-291.
Affiliations
  1. Department of Neurosurgery, West China Hospital, Sichuan University, Chengdu
  2. Department of Radiology, West China Hospital, Sichuan University, Chengdu
  3. Department of Pathology, West China Hospital, Sichuan University, Chengdu

open access

Vol 48, No 4 (2014)
Case reports
Submitted: 2014-02-22

Abstract

Intracranial extraskeletal mesenchymal chondrosarcoma is a very rare malignant tumor with predilection site of frontoparietal falx cerebri. Only few cases of mesenchymal chondrosarcoma in posterior cranial fossa are reported. Here, we report a 23-year-old young man with a dura-attached mass in left posterior cranial fossa misdiagnosed as a tentorial meningioma preoperatively. According to the following operation, the lesion was confirmed as mesenchymal chondrosarcoma surgically and pathologically. On MRI, the tumor was characterized by lobulated soft-tissue mass with dura-attached base, patchy calcifications and heterogeneous signal intensities. On contrast-enhanced MRI, it was well-defined, with marked enhancement. We consider that these imaging features above might remind us to consider the diagnosis of mesenchymal chondrosarcoma in posterior cranial fossa. The postoperative treatment of radiotherapy is still controversial. As for our case, according to the 24 months follow-up after postoperative γ-knife, our patient shows an optimistic prognosis so far.

Abstract

Intracranial extraskeletal mesenchymal chondrosarcoma is a very rare malignant tumor with predilection site of frontoparietal falx cerebri. Only few cases of mesenchymal chondrosarcoma in posterior cranial fossa are reported. Here, we report a 23-year-old young man with a dura-attached mass in left posterior cranial fossa misdiagnosed as a tentorial meningioma preoperatively. According to the following operation, the lesion was confirmed as mesenchymal chondrosarcoma surgically and pathologically. On MRI, the tumor was characterized by lobulated soft-tissue mass with dura-attached base, patchy calcifications and heterogeneous signal intensities. On contrast-enhanced MRI, it was well-defined, with marked enhancement. We consider that these imaging features above might remind us to consider the diagnosis of mesenchymal chondrosarcoma in posterior cranial fossa. The postoperative treatment of radiotherapy is still controversial. As for our case, according to the 24 months follow-up after postoperative γ-knife, our patient shows an optimistic prognosis so far.

Get Citation

Keywords

Posterior cranial fossa, Tentorium cerebella, Mesenchymal chondrosarcoma, Computerized Tomography, Magnetic Resonance Imaging

About this article
Title

A rare tentorial mesenchymal chondrosarcoma in posterior cranial fossa: Case report

Journal

Neurologia i Neurochirurgia Polska

Issue

Vol 48, No 4 (2014)

Pages

287-291

Page views

314

Article views/downloads

633

DOI

10.1016/j.pjnns.2014.06.001

Bibliographic record

Neurol Neurochir Pol 2014;48(4):287-291.

Keywords

Posterior cranial fossa
Tentorium cerebella
Mesenchymal chondrosarcoma
Computerized Tomography
Magnetic Resonance Imaging

Authors

Anqi Xiao
Zhenlin Li
Xin He
Chao You

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