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Background: Dural chondrosarcoma is a very rare intracranial tumor, given that meninges do not normally contain cartilaginous tissue from which it can originate. We present a case of primary extraosseous dural chondrosarcoma.
Case Presentation: A 48-year-old woman presented to our tertiary center neurosurgery consultation with progressive headache, vomiting, vertigo, and gait instability of 5 months' duration. An initial brain CT revealed a large parietal mass with gross calcifications and subtle hyperostosis of the inner table. Subsequent brain MRI showed a heterogeneous expansive lesion with a honey-comb enhancement. Discussion of intra- or extra-axial location was warranted, and finally, initial presurgical suspicion of meningioma arose although some atypical imaging features were detected. The differential diagnosis included solitary fibrous tumor-hemangiopericytoma and dural metastasis. Total resection of the lesion was performed, extra-axial origin was confirmed, and pathology resulted in a primary dural chondrosarcoma.
Conclusion: The importance of this case presentation lies in the unusual nature of the final diagnosis, the brief literature review and differential diagnosis with emphasis on imaging pearls, as well as the useful reminder for physicians to consider less frequent diseases when key findings do not unambiguously lead to the usual suspects.
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http://dx.doi.org/10.1186/s12883-021-02515-y | DOI Listing |
Cureus
July 2025
Pathology, Guntur Medical College, Guntur, IND.
Primary vulvar Ewing sarcoma (ES) is exceedingly rare, particularly in postmenopausal women. To date, only 14 cases have been confirmed through molecular cytogenetic analysis. We report the case of a 55-year-old woman presenting with a painful, ulcerated vulvar mass.
View Article and Find Full Text PDFHead Neck
August 2025
Head of the Research, Development, and Technological Innovation Department, Fundación Oftalmológica de Santander, Floridablanca, Colombia.
Background: Extraosseous Ewing sarcomas account for approximately 20%-30% of all Ewing sarcomas. Among these, 5%-10% occur in the head and neck region, representing approximately 1%-3% of all Ewing sarcomas.
Methods: We report the case of a 33-year-old female patient with a progressively enlarging mass in the frontal scalp over the course of 18 months.
Int J Surg Case Rep
August 2025
Urology Department, University of Medicine and Pharmacy at Ho Chi Minh City, 217 Hong Bang Street, Ward 11, District 5, Ho Chi Minh City 70000, Viet Nam; Urology Department, University Medical Center, 215 Hong Bang Street, Ward 11, District 5, Ho Chi Minh City 70000, Viet Nam; Binh Dan Hospital, Ho
Introduction And Importance: Primary renal extraosseous osteosarcoma is a rare, aggressive tumor with nonspecific features, often diagnosed via histopathology and immunohistochemistry.
Case Presentation: A 56-year-old man with no symptoms was incidentally found to have a calcified left renal mass on contrast-enhanced CT during routine health screening. Imaging showed a 4 × 5 × 5 cm heterogeneous lesion at the renal hilum, abutting the left psoas muscle.
Cancers (Basel)
August 2025
Department of Orthopaedics and Sports Orthopaedics, TUM Klinkum Rechts der Isar, Ismaninger Str. 22, 81675 Munich, Germany.
Background/objectives: The quality of surgical margins has been shown to be a prognostic factor in many sarcoma entities, yet its role in osteosarcoma remains controversial. While previous studies have shown that the outcome was not related to the margin width in bone, the impact of the extraosseous margin width (margin at the soft tissue invasion)-which needs to be close sometimes due to neurovascular structures-needs to be assessed. This study aims to evaluate the influence of soft tissue surgical margins on local recurrence and overall survival in patients with high-grade osteosarcoma.
View Article and Find Full Text PDFJ Neurosurg Case Lessons
July 2025
Virginia Tech Carilion School of Medicine, Roanoke, Virginia.
Background: Ewing sarcoma is a rare malignant tumor that primarily affects children and young adults, commonly metastasizing to the lungs, bone, and bone marrow. CNS involvement is extremely rare, especially with the primary presentation of intracranial hemorrhage. Current protocols do not include routine neuroimaging, potentially delaying the detection of brain metastasis.
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