Literature DB >> 21415692

Radiographic evidence of regression of a solitary osteochondroma: a report of 4 cases and a literature review.

Angela M Passanise1, Charles T Mehlman, Eric J Wall, Jason P Dieterle.   

Abstract

Solitary osteochondromas are considered to be the most common benign bone tumor. Slow progressive osteochondroma growth is the rule in skeletally immature patients, at times prompting surgical excision. Significant growth of a lesion beyond skeletal maturity is commonly considered to be a harbinger of malignant transformation. Although spontaneous regressions of these lesions are sporadically reported in the literature, most practitioners consider spontaneous regression of an existing solitary osteochondroma to be extremely unlikely. The purpose of this case report was to offer a collection of 4 new well-documented cases of radiographic evidence of regression of solitary osteochondromas in skeletally immature patients. A review of the literature is also presented. Twenty cases have been reported in the literature on spontaneously regressing solitary osteochondromas, with approximately 50% of the cases in radiology journals, and never more than 2 cases having been reported at one time, until now. Asymptomatic solitary osteochondromas may not be diagnosed or lack long-term follow-up, thereby contributing to the true unknown incidence of resolving osteochondromas. Although there are now only 24 documented cases in the literature of solitary osteochondromas that have spontaneously regressed, the rarity of this lesion is completely uncertain, as most go undiagnosed. The review of the suggested mechanisms by which solitary osteochondromas spontaneously regress is presented. Surgical excision is not without risk, with reported complication rates as high as 12.5%. These cases demonstrate that osteochondromas can actually resolve, and that conservative treatment by observation and yearly radiographs is an option for these lesions, especially in an asymptomatic pediatric patient. From the review of the literature most lesions were resolving before skeletal maturity and within 3 years of identification. Lesions that are symptomatic can be treated according to the patient's symptoms. This information should prove to be useful for patients and treating physicians when discussing treatment options for solitary osteochondromas, and reduce unnecessary surgery for these lesions.

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Year:  2011        PMID: 21415692     DOI: 10.1097/BPO.0b013e31820fc676

Source DB:  PubMed          Journal:  J Pediatr Orthop        ISSN: 0271-6798            Impact factor:   2.324


  10 in total

Review 1.  Hereditary Multiple Exostoses: a review of clinical appearance and metabolic pattern.

Authors:  Giovanni Beltrami; Gabriele Ristori; Guido Scoccianti; Angela Tamburini; Rodolfo Capanna
Journal:  Clin Cases Miner Bone Metab       Date:  2016-10-05

2.  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

3.  Computer Navigation-Aided Excision of Proximal Femoral Osteochondroma: Surgical Technique.

Authors:  Yang Sun; Chun Ming Chan; Feng Yu; Yuan Li; Xiaohui Niu
Journal:  Comput Math Methods Med       Date:  2022-05-31       Impact factor: 2.809

4.  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

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.  Regression of a solitary osteochondroma of the distal humerus in a toddler following trauma.

Authors:  Paul B Heyworth; Muddassir Rashid
Journal:  Radiol Case Rep       Date:  2018-11-07

7.  An unusual diagnosis for an usual test.

Authors:  Andrea Trombetta; Vanessa Migliarino; Flavio Faletra; Egidio Barbi; Gianluca Tornese
Journal:  Ital J Pediatr       Date:  2020-06-10       Impact factor: 2.638

Review 8.  Hereditary Multiple Exostoses: Current Insights.

Authors:  Antonio D'Arienzo; Lorenzo Andreani; Federico Sacchetti; Simone Colangeli; Rodolfo Capanna
Journal:  Orthop Res Rev       Date:  2019-12-13

9.  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

Review 10.  Atypical osteochondroma of the hamate that presented clinically as carpal tunnel syndrome: report of an extremely rare case and literature review.

Authors:  Makoto Motomiya; Taiki Sakazaki; Norimasa Iwasaki
Journal:  BMC Musculoskelet Disord       Date:  2020-04-13       Impact factor: 2.362

  10 in total

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