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Osteochondromyxoma

MedGen UID:
824952
•Concept ID:
C3839106
•
Neoplastic Process
SNOMED CT: Osteochondromyxoma (703695006)
 
HPO: HP:0034951

Definition

A rare benign chondroid and osteoid matrix-producing neoplasm of bone characterized by extensive myxoid changes. OMX originate from bony cortices and have been observed in the nasal region, as well as the tibia and radius. [from HPO]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVOsteochondromyxoma

Professional guidelines

PubMed

MANAGEMENT OF ENDOCRINE DISEASE: Carney complex: clinical and genetic update 20 years after the identification of the CNC1 (PRKAR1A) gene.
Bouys L, Bertherat J
Eur J Endocrinol 2021 Mar;184(3):R99-R109. doi: 10.1530/EJE-20-1120. PMID: 33444222

Recent clinical studies

Etiology

Congenital bizarre parosteal osteochondromatous proliferation in unusual location and age: a case report.
Sökücü S, Aycan OE, Arıkan Y, Kabukçuoğlu YS
Acta Orthop Traumatol Turc 2016;50(1):120-4. doi: 10.3944/AOTT.2016.13.0141. PMID: 26854060

Diagnosis

An adolescent case of sellar osteochondromyxoma in the setting of spondyloepiphyseal dysplasia.
Peng S, Behbahani M, Sharma S, Wadhwani NR, Rastatter JC, Alden TD
Childs Nerv Syst 2023 Apr;39(4):1083-1087. Epub 2023 Feb 1 doi: 10.1007/s00381-022-05786-z. PMID: 36723686
An Unusual Presentation of Carney Complex.
Dağdeviren Çakır A, Turan H, Celkan T, Çomunoğlu N, Ercan O, Evliyaoğlu O
J Clin Res Pediatr Endocrinol 2020 Mar 19;12(1):117-121. Epub 2019 May 23 doi: 10.4274/jcrpe.galenos.2019.2019.0043. PMID: 31117334Free PMC Article
Congenital bizarre parosteal osteochondromatous proliferation in unusual location and age: a case report.
Sökücü S, Aycan OE, Arıkan Y, Kabukçuoğlu YS
Acta Orthop Traumatol Turc 2016;50(1):120-4. doi: 10.3944/AOTT.2016.13.0141. PMID: 26854060
Translocation t(12;17)(q24.1;q21) as the sole anomaly in a nasal chondromesenchymal hamartoma arising in a patient with pleuropulmonary blastoma.
Behery RE, Bedrnicek J, Lazenby A, Nelson M, Grove J, Huang D, Smith R, Bridge JA
Pediatr Dev Pathol 2012 May-Jun;15(3):249-53. Epub 2012 Feb 22 doi: 10.2350/11-11-1121-CR.1. PMID: 22356457
Rare syndromes.
Jabbour SA, Davidovici BB, Wolf R
Clin Dermatol 2006 Jul-Aug;24(4):299-316. doi: 10.1016/j.clindermatol.2006.04.005. PMID: 16828412

Prognosis

Osteochondromyxoma of bone: a congenital tumor associated with lentigines and other unusual disorders.
Carney JA, Boccon-Gibod L, Jarka DE, Tanaka Y, Swee RG, Unni KK, Stratakis CA
Am J Surg Pathol 2001 Feb;25(2):164-76. doi: 10.1097/00000478-200102000-00004. PMID: 11176065

Clinical prediction guides

Congenital bizarre parosteal osteochondromatous proliferation in unusual location and age: a case report.
Sökücü S, Aycan OE, Arıkan Y, Kabukçuoğlu YS
Acta Orthop Traumatol Turc 2016;50(1):120-4. doi: 10.3944/AOTT.2016.13.0141. PMID: 26854060
Osteochondromyxoma of bone: a congenital tumor associated with lentigines and other unusual disorders.
Carney JA, Boccon-Gibod L, Jarka DE, Tanaka Y, Swee RG, Unni KK, Stratakis CA
Am J Surg Pathol 2001 Feb;25(2):164-76. doi: 10.1097/00000478-200102000-00004. PMID: 11176065

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