Clinicopathological and histological behavior of mesenchymal chondrosarcoma involving maxilla (original) (raw)

Mesenchymal chondrosarcoma of maxilla in paediatric patient

BMJ Case Reports, 2019

Chondrosarcoma (CS) is a malignant tumour of long and flat bone characterised by the formation of cartilage. Mesenchymal chondrosarcoma (MCS) is a rare subtype of CS that is more aggressive and may lead to erroneous diagnosis in a limited biopsy. The diagnosis is mainly based on the histopathological appearance of biphasic pattern of undifferentiated small round cells separated by islands of well-differentiated hyaline cartilage. We report a case of 13-year-old boy who initially presented with gum swelling and the biopsy result suggested a benign fibrous lesion. Following an extensive lesion shown in radiologic findings, the tumour excision was done and finally was diagnosed as an MCS of the maxilla. The patient was given postoperative chemotherapy (EURO-EWING 99 regimen), and now on regular follow-up for monitoring of local recurrence or tumour metastasis.

Mesenchymal chondrosarcoma of the maxilla

The Journal of Laryngology & Otology, 1994

We report, to our knowledge, the 10th recorded case of mesenchymal chondrosarcoma (MC) occurring in the maxilla. Our case is the youngest person reported with a tumour in this location. The prognosis for cure is poor with a high incidence of local recurrence as well as metastases. Treatment is based on radical surgery. Radiotherapy and chemotherapy have a adjuvant role but additional experience with this tumour is required to define the most efficacious treatment.

Mesenchymal Chondrosarcoma of the Mandible

Asian Journal of Oral and Maxillofacial Surgery, 2008

This report describes a 33-year-old man diagnosed with mesenchymal chondrosarcoma. The patient was referred with a painless, elastic hard mass in the retromolar region. Radiologically, the tumour presented as an expansion of the right mandibular ramus partly extending to the inferior masseter. A segmental mandibulectomy was performed during the initial surgery. Histopathologically, the tumour showed well-differentiated hyaline cartilage tissue in the lobules with cartilaginous islands and small cells. Immunohistochemically, the tumour cells reacted positively to clusters of differentiation99 and S-100 protein. The tumour recurred in the right inferior temporal fossa 3 years after the initial surgery. Although radical right maxillectomy and dissection of the inferior temporal fossa were carried out immediately, the patient developed multiple pulmonary metastases after 10 months.

Mesenchymal Mandibular Chondrosarcoma: A Case Report and Review of Literature

Open Journal of Stomatology

Introduction: Chondrosarcomas (CS) are malignant cartilaginous tumors of rare maxillary localization. Their evolution is generally slow in time. They have a high tendency for locoregional recurrence after surgical treatment. Their prognosis depends on their degree of differentiation and the quality of resection. The authors report a clinical case of mesenchymal mandibular chondrosarcoma (MC), which is considered to be a subtype of CS, and specify the epidemiological, diagnostic, therapeutic and evolutionary features of this tumor. Case Report: A 73-year-old woman reported in February 2018 in our department complained of a slowly enlarging mass involving the right part of the lower jaw for the last 18 months. On examination a firm multilobular painful mass was palpated with cortical expansion, occupying the right side. A CT scan with 3D reconstruction was achieved and showed osteolysis lesions and cortical thickening. The mass biopsy for histological examination found a grade I well-differentiated bone chondrosarcoma. We performed a hemi-mandibulectomy with complete resection of the tumor. The anatomopathologic examination of the resection specimen was in favour of a grade II mesenchymal chondrosarcoma. No radiotherapy was needed. The patient's follow up was uneventful. Discussion: CS grading is the key to its management. Low grade CS (grades I and II) of the facial skeleton are luckily the most common, they are best treated with a local resection using 1.5 cm margins for bone and soft tissue. According to published literature, CS was historically considered as a radio resistant tumor. Radiotherapy and chemotherapy were therefore mainly reserved for high-grade tumors and for non-operable lesions. However, radical local surgery appears to be the treatment of choice for low grade chondrosarcoma. Conclusion: CS's definitive diagnosis depends on appropriate radiographic evaluation along with adequate biopsy with meticulous histopathological examination and adjunctive immunohistochimical analysis. Neither chemotherapy nor radiotherapy is indicated as primary treatment. A long period follow-up should be advised as recurrence How to cite this paper: Abouchadi, A.,

Mesenchymal Chondrosarcoma of the Jaws: A Series of two Rare Cases

2012

Chondrosarcoma (CS) is a malignant neoplasm that results in abnormal bone and cartilage growth. Although CS is rare, it is the second most common primary bone malignancy. Mesenchymal chondrosarcoma (MC) is a rare histological variant of CS that accounts for only about 1% of all CS and has high predilection for the head and neck region. It is usually seen in younger age group compared to conventional CS and the maxillary alveolus is the most common site. The tumor is unique because of its aggressive growth with a high tendency for late recurrence and delayed metastasis. We present two cases of MC, one case involving the mandibular condyle and the second, a metastatic CS with the primary in the clavicle.

Mesenchymal chondrosarcoma: An unusual lump in posterior maxilla

International Journal of Case Reports and Images, 2017

International Journal of Case Reports and Images (IJCRI) is an international, peer reviewed, monthly, open access, online journal, publishing high-quality, articles in all areas of basic medical sciences and clinical specialties. Aim of IJCRI is to encourage the publication of new information by providing a platform for reporting of unique, unusual and rare cases which enhance understanding of disease process, its diagnosis, management and clinico-pathologic correlations. IJCRI publishes Review Articles, Case Series, Case Reports, Case in Images, Clinical Images and Letters to Editor.

Chondrosarcoma of the maxilla. Case report.

Anil, S., V. T. Beena, et al. (1998). "Chondrosarcoma of the maxilla. Case report." Australian dental journal 43(3): 172-174. Chondrosarcoma is a rare malignant neoplasm of the jaws. The diagnosis of this lesion is mainly based on the histopathological appearance. A case of chondrosarcoma of the maxilla is reported. The origin of this rare tumor in the maxilla, a bone with exclusive membranous ossification, is discussed.