The authors report a new case of mesenchymal chondrosarcoma (MCS), occurring in the upper jaw bone of a 19 year-old woman. Radiographic picture in the bone shows an aggressive osteolytic tumor suspect of malignancy. An incisional biopsy was practiced and the histologic examination has confirmed the diagnosis of MCS. Treatment have consisted of a large resection of maxilla with additional irradiation therapy. The postoperative course was marked by recurrence of the lesion one year later.
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Cir Cir
October 2005
Instituto Nacional de Cancerología, Omecihuatl 37, Col. Adolfo Ruiz Cortines, 04630 México, D.F., México.
Maffucci syndrome is a rare, congenital disease, which is associated with the appearance of multiple enchondromas (possibility of malignant transformation in 20 to 100%), soft tissue hemangiomas and other mesenchymatous injuries. Case 1 is a 33-year-old female who presented with multiple nodules predominantly in upper extremities. Upon examination, there was deformity in articulation and nodules on the hands, which were soft and moveable.
View Article and Find Full Text PDFRev Chir Orthop Reparatrice Appar Mot
May 2004
Service d'Anatomie et de Cytologie Pathologiques, Institut Salah Azaiez-Bab Saadoun, 1006 Tunis, Tunisie.
We report a new case of mesenchymal chondrosarcoma in a 25-Year-old woman who presented a tumefaction of the anteromedial aspect of the mid left leg which had developed over two Years. Computed tomography of the lower left limb demonstrated the presence of a soft tIssue tumor limited to the gastrocnemus medial. The 7.
View Article and Find Full Text PDFTunis Med
January 2001
Service d'anatomie pathologique, Hôpital Charles Nicolle, Tunis.
The authors report a new case of mesenchymal chondrosarcoma (MCS), occurring in the upper jaw bone of a 19 year-old woman. Radiographic picture in the bone shows an aggressive osteolytic tumor suspect of malignancy. An incisional biopsy was practiced and the histologic examination has confirmed the diagnosis of MCS.
View Article and Find Full Text PDFNeurochirurgie
March 1996
Service de Neurochirurgie, Hôpital Sainte-Marguerite, Marseille.
The authors report a case of chondrosarcoma of the skull base with a myxoïd histology, developed from the right sphenotemporal junction. Twenty six months after enlarged tumour removal, there are no clinical or neuroradiological signs of recurrence. A review of the 180 published cases emphasizes the rarity of this tumour originating of the skull base synchondrosis and occurring in young patients.
View Article and Find Full Text PDFNeurochirurgie
March 1990
Hôpital Neurologique et Neurochirurgical Pierre-Wertheimer, Lyon.
Cartilaginous tumours represent 0.16% of all intracranial tumours; among them 14% are chondrosarcomas (Ch-S). A majority (56%) arise from the skull base, especially from the spheno-occipital and spheno-temporal synchondroses.
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