Literature DB >> 20415917

Parosteal osteosarcoma: report of a case and review of the literature.

T C Huang1, P A Monsour, C D Chahoud.   

Abstract

Parosteal osteosarcoma is a rare malignancy of the bone that usually arises in the long bones. Involvement of the oral cavity is rare. Only 12 cases of intraoral parosteal osteosarcoma have been reported in the English language literature. This paper defines the major clinical, radiographic and histologic features of parosteal osteosarcoma and illustrates these with a case of a 33-year-old male presenting with a three-month history of a painless enlarging lump in the right maxilla. A critical and comprehensive review of the English language literature is also provided.

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Year:  2010        PMID: 20415917     DOI: 10.1111/j.1834-7819.2009.01175.x

Source DB:  PubMed          Journal:  Aust Dent J        ISSN: 0045-0421            Impact factor:   2.291


  5 in total

1.  A large heterotopic ossification in a 25 years old laparotomy scar.

Authors:  Robbert J H van Leeuwen; Tim Kraal; Sander Scholtens; Gijs Visser
Journal:  Quant Imaging Med Surg       Date:  2016-08

Review 2.  Proposed Clinico-Pathological Classification for Oral Exophytic Lesions.

Authors:  Arvind Babu Rajendra Santosh; Doryck Boyd; Kumaraswamy Kikeri Laxminarayana
Journal:  J Clin Diagn Res       Date:  2015-09-01

3.  Parosteal osteosarcoma: Report of a rare juxtacortical variant of osteosarcoma affecting the maxilla.

Authors:  Surekha Rudrayya Puranik; Rudrayya Shivanand Puranik; Praveen Kumar Ramdurg; Gunjan Ram Chandra Choudhary
Journal:  J Oral Maxillofac Pathol       Date:  2014 Sep-Dec

4.  Chondrosarcoma of maxilla.

Authors:  Asha Karadwal; Shailja Chatterjee
Journal:  J Oral Maxillofac Pathol       Date:  2018-01

5.  Parosteal Osteosarcoma: A Benign-Looking Tumour, Amenable to a Variety of Surgical Reconstruction.

Authors:  Yogi Prabowo; Achmad Fauzi Kamal; Evelina Kodrat; Marcel Prasetyo; Samuel Maruanaya; Toto Suryo Efar
Journal:  Int J Surg Oncol       Date:  2020-05-28
  5 in total

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