منابع مشابه
Intracranial extraskeletal mesenchymal chondrosarcoma.
Intracranial extraskeletal mesenchymal chondrosarcoma is a rare malignant variant of chondrosarcomas. We present a 5-year-old Saudi male child who was brought to the Emergency Department with the complaints of headache, irritability, vomiting, and unsteadiness of gait with right hemiparesis. Radiological studies confirmed the presence of a space-occupying lesion in the left cerebral hemisphere ...
متن کاملManagement of renal extraskeletal mesenchymal chondrosarcoma
BACKGROUND Primary mesenchymal chondrosarcoma of the kidney is an extremely rare malignant tumor. To our best knowledge, only 9 such cases have been reported so far. CASE PRESENTATION In the current paper, we present the case of a 67 year-old patient with recurrent left lumbar pain, increased fatigability and intermittent macroscopic hematuria. He underwent a surgical resection of the left ki...
متن کاملPrimary extraskeletal mesenchymal chondrosarcoma of the vulva
Extraskeletal chondrosarcoma is rare, making up only 1% of reported chondrosarcoma. We experienced 3 cases of extraskeletal chondrosarcoma, especially in vulva. They were suspected as lipoma of the vulva. The patients had noticed a small but growing mass on their vulva which had been palpated earlier. The masses were excised with a 2 cm resection margin. The final pathological reports confirmed...
متن کاملRetroperitoneal Extraskeletal Mesenchymal Chondrosarcoma: A Very Rare Case Report
Chondrosarcoma is an uncommon malignant neoplasm of cartilaginous origin. Extraskeletal chondrosarcomas are far less common than their intraosseous counterparts, representing approximately 2% of all soft tissue sarcomas. Clinically, extraskeletal mesenchymal chondrosarcoma (EMC) shows a very fast progression. It also has a high incidence of local recurrence and distant metastasis. The most comm...
متن کاملExtraskeletal Mesenchymal Chondrosarcoma of Shoulder: An Extremely Rare Case
INTRODUCTION Extraskeletal chondrosarcoma (EMC) is a rare, aggressive neoplasm which has been seen in the soft tissue area. This soft tissue sarcoma is classified to myxoid and mesenchymal based on histologic criteria. The mesenchymal subtype has a poor prognosis. In approximately 50% of patient with EMC, we could observe soft tissue lesion and stippled calcification in the conventional radiogr...
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ژورنال
عنوان ژورنال: Archives of Pathology & Laboratory Medicine
سال: 2018
ISSN: 0003-9985,1543-2165
DOI: 10.5858/arpa.2017-0109-rs