Literature DB >> 24172645

Spontaneous resolution of a solitary osteochondroma of the distal femur: a case report and review of the literature.

Christopher E Hill1, Lenetta Boyce, Irene D van der Ploeg.   

Abstract

Osteochondromata are common, benign tumours mainly affecting long-bone metaphyses. They comprise 35% of all primary benign bone tumours and 8% of all bone tumours overall, although their true incidence is unknown as many remain undiagnosed. They can cause multiple symptoms including pain and referral for excision is not uncommon. What is less recognized is their potential for spontaneous regression, a phenomenon that renders excision surgery, with its potential risks, unnecessary. We present an illustrated case of a spontaneously resolved, solitary osteochondroma in a young male, highlighting that solitary osteochondromata can actually resolve and in the asymptomatic child, a period of watchful waiting can be an appropriate option, avoiding a potentially unnecessary surgical excision with recognized complications.

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Year:  2014        PMID: 24172645     DOI: 10.1097/BPB.0000000000000010

Source DB:  PubMed          Journal:  J Pediatr Orthop B        ISSN: 1060-152X            Impact factor:   1.041


  6 in total

1.  Spontaneous shrinkage of solitary osteochondromas.

Authors:  Hisaki Aiba; Satoshi Yamada; Norio Yamamoto; Katsuhiro Hayashi; Shinji Miwa; Hiroyuki Tsuchiya; Takanobu Otsuka
Journal:  Skeletal Radiol       Date:  2017-08-19       Impact factor: 2.199

2.  An Osteological Study on the Prevalence of Osteochondromas.

Authors:  Gregory R Gaumer; Doug S Weinberg; Christopher D Collier; Patrick J Getty; Raymond W Liu
Journal:  Iowa Orthop J       Date:  2017

3.  Magnetic resonance imaging follow-up of chondroid tumors: regression vs. progression.

Authors:  Bo Mi Chung; Sung Hwan Hong; Hye Jin Yoo; Ja-Young Choi; Hee-Dong Chae; Dong Hyun Kim
Journal:  Skeletal Radiol       Date:  2017-12-03       Impact factor: 2.199

4.  Multiple Hereditary Exostoses: Report of an EXT2 Gene Mutation in a Colombian Family.

Authors:  Jhon Camacho; Luz Dary Gutierrez; Cladelis Rubio; Alfonso Suárez; Angie Amaya
Journal:  J Pediatr Genet       Date:  2018-03-07

5.  Daughter and mother diagnosed with hereditary multiple exostoses: A case report and a review of the literature.

Authors:  Cristina Oana Mărginean; Lorena Elena Meliţ; Maria Oana Mărginean
Journal:  Medicine (Baltimore)       Date:  2017-01       Impact factor: 1.889

6.  Hereditary multiple exostoses and solitary osteochondroma associated with growth hormone deficiency: to treat or not to treat?

Authors:  Mauro Bozzola; Chiara Gertosio; Maria Gnoli; Federico Baronio; Elena Pedrini; Cristina Meazza; Luca Sangiorgi
Journal:  Ital J Pediatr       Date:  2015-08-04       Impact factor: 2.638

  6 in total

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