mesenchymal chondrosarcoma: a report of two cases with immunohistochemical study

Authors

reeby sara thomas

herald j sherlin

anuja natesan

priya premkumar

pratibha ramani

abstract

mesenchymal chondrosarcoma (mc) is an uncommon tumor with an aggressive behaviour. we present two cases of mc. the first one is a unique case of mc of the maxilla metastasized from the clavicle. the second describes mc in the mandible with extensive involvement of the condyle. a 31-year-old male and a 22-year-old male presented to saveetha dental college, with a 2-month history of progressive mass in left posterior maxilla and a firm swelling in the right mandibular region, respectively. incisional biopsy of both the cases revealed characteristic bimorphic pattern composed of sheets of undifferentiated round and spindle cells along with areas of chondroid matrix of variable cellularity. histopathological features were suggestive of mc.  these type of neoplams show local aggressive behaviour with high metastatic and recurrence potential due to which the prognosis of mc is poor.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

Mesenchymal Chondrosarcoma: A Report of Two Cases with Immunohistochemical Study

  Mesenchymal chondrosarcoma (MC) is an uncommon tumor with an aggressive behaviour. We present two cases of MC. The first one is a unique case of MC of the maxilla metastasized from the clavicle. The second describes MC in the mandible with extensive involvement of the condyle. A 31-year-old male and a 22-year-old male presented to Saveetha Dental College, with a 2-month history of progressiv...

full text

Mesenchymal Chondrosarcoma: A Report of Two Cases with Immunohistochemical Study

Mesenchymal chondrosarcoma (MC) is an uncommon tumor with an aggressive behaviour. We present two cases of MC. The first one is a unique case of MC of the maxilla metastasized from the clavicle. The second describes MC in the mandible with extensive involvement of the condyle. A 31-year-old male and a 22-year-old male presented to Saveetha Dental College, with a 2-month history of progressive m...

full text

Mesenchymal chondrosarcoma: a case report.

Mesenchymal chondrosarcoma is a rare disease with poor prognosis. Treatment including wide or radical excision is very important. Radiotherapy and chemotherapy are additional treatment options, but no conclusive results for their efficacy have been shown until date. Imaging modalities can give important clues for diagnosis and management planning. Angioembolization before surgery could be usefu...

full text

Extraskeletal myxoid chondrosarcoma: A report of two cases

Extraskeletal myxoid chondrosarcoma (EMC) is a relatively rare but well-defined neoplasm. This report describes two patients, one with EMC of the buttock and one with EMC of the knee. The two cases presented with large lobed masses and long T1 and T2 signaling identified by magnetic resonance imaging (MRI). An enhanced MRI scan demonstrated enhancement of the tumors. The tumors were composed of...

full text

Harlequin Ichthyosis: A report of two cases

Harlequin ichthyosis is one of the most severe congenital skin cornification disorders with an incidence rate of about 1 in 300000 births and characteristic clinical features. We report two cases of harlequin ichthyosis (HI) or harlequin fetus (HF), which were products of consanguineous union. Clinical examination showed typical features of harlequin ichthyosis, with the presence of plaques wit...

full text

Pituitary Abscess: a Report of Two Cases

Background and Importance: Abscess of the hypophysis or pituitary adenoma is a very rare entity, and its preoperative diagnosis could be challenging. The clinical presentation is less specific, and despite the recent advancement in imaging, diagnosis before surgery is still difficult. Case Presentation: We reported two cases of pituitary abscesses in patients aged 38 and 42 years. The first ...

full text

My Resources

Save resource for easier access later


Journal title:
iranian journal of pathology

Publisher: iranian society of pathology

ISSN 1735-5303

volume 5

issue 2 2010

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023