Literature DB >> 11828332

Malignant transformation of fibrous dysplasia into chondroblastic osteosarcoma.

Shaifali Kaushik1, Wendy R K Smoker, William J Frable.   

Abstract

A case of malignant transformation of polyostotic fibrous dysplasia into maxillary chondroblastic osteosarcoma is presented. The clinical, radiographic, CT, MR imaging features and pathological findings of polyostotic fibrous dysplasia and its malignant transformation are described. Malignant transformation of fibrous dysplasia is rare and has not previously been described in the English literature in this location in McCune-Albright syndrome and in the absence of radiation treatment.

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Mesh:

Year:  2001        PMID: 11828332     DOI: 10.1007/s002560100436

Source DB:  PubMed          Journal:  Skeletal Radiol        ISSN: 0364-2348            Impact factor:   2.199


  15 in total

1.  Associations of polymorphisms in the bone morphogenetic protein-2 gene with risk and prognosis of osteosarcoma in a Chinese population.

Authors:  Yu Cong; Cheng-Jun Li; Jian-Ning Zhao; Xiao-Zhou Liu; Xin Shi
Journal:  Tumour Biol       Date:  2014-11-13

2.  Dental perspectives in fibrous dysplasia and McCune-Albright syndrome.

Authors:  Sunday O Akintoye; Alison M Boyce; Michael T Collins
Journal:  Oral Surg Oral Med Oral Pathol Oral Radiol       Date:  2013-09

Review 3.  [Bisphosphonates in the therapy of fibrous dysplasia. Relevant data and practical aspects].

Authors:  Sigrun Egner-Höbarth; H Welkerling; R Windhager
Journal:  Orthopade       Date:  2007-02       Impact factor: 1.087

4.  Malignant sarcomatous transformation of fibrous dysplasia.

Authors:  Stacey K Mardekian; Madalina Tuluc
Journal:  Head Neck Pathol       Date:  2014-08-27

5.  McCune-Albright syndrome: surgical and therapeutic challenges in GH-secreting pituitary adenomas.

Authors:  Helen Madsen; Manuel Thomas Borges; Janice M Kerr; Kevin O Lillehei; B K Kleinschmidt-Demasters
Journal:  J Neurooncol       Date:  2010-11-21       Impact factor: 4.130

Review 6.  DIAGNOSIS OF ENDOCRINE DISEASE: Mosaic disorders of FGF23 excess: Fibrous dysplasia/McCune-Albright syndrome and cutaneous skeletal hypophosphatemia syndrome.

Authors:  Luis F de Castro; Diana Ovejero; Alison M Boyce
Journal:  Eur J Endocrinol       Date:  2020-05       Impact factor: 6.664

Review 7.  Clinical and molecular genetics of acromegaly: MEN1, Carney complex, McCune-Albright syndrome, familial acromegaly and genetic defects in sporadic tumors.

Authors:  Anelia Horvath; Constantine A Stratakis
Journal:  Rev Endocr Metab Disord       Date:  2008-03       Impact factor: 6.514

8.  Advances in the Diagnosis, Treatment, and Molecular Genetics of Pituitary Adenomas in Childhood.

Authors:  Margaret F Keil; Constantine A Stratakis
Journal:  US Endocrinol       Date:  2009-02-01

Review 9.  Pituitary tumors in childhood: update of diagnosis, treatment and molecular genetics.

Authors:  Margaret F Keil; Constantine A Stratakis
Journal:  Expert Rev Neurother       Date:  2008-04       Impact factor: 4.618

Review 10.  Acromegaly and McCune-Albright syndrome.

Authors:  Sylvie Salenave; Alison M Boyce; Michael T Collins; Philippe Chanson
Journal:  J Clin Endocrinol Metab       Date:  2014-02-11       Impact factor: 5.958

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