Multimodality imaging features of USP6-associated neoplasms

Skeletal Radiol. 2023 Mar;52(3):297-313. doi: 10.1007/s00256-022-04146-x. Epub 2022 Aug 13.

Abstract

Since the discovery of USP6 gene rearrangements in aneurysmal bone cysts nearly 20 years ago, we have come to recognize that there is a family of USP6-driven mesenchymal neoplasms with overlapping clinical, morphologic, and imaging features. This family of neoplasms now includes myositis ossificans, aneurysmal bone cyst, nodular fasciitis, fibroma of tendon sheath, fibro-osseous pseudotumor of digits, and their associated variants. While generally benign and in many cases self-limiting, these lesions may undergo rapid growth, and be confused with malignant bone and soft tissue lesions, both clinically and on imaging. The purpose of this article is to review the imaging characteristics of the spectrum of USP6-driven neoplasms, highlight key features that allow distinction from malignant bone or soft tissue lesions, and discuss the role of imaging and molecular analysis in diagnosis.

Keywords: ABC; Aneurysmal bone cyst; FOPD; Fibro-osseous pseudotumor of digits; Fibroma of tendon sheath; Myositis ossificans; Nodular fasciitis; USP6.

Publication types

  • Review

MeSH terms

  • Bone Cysts, Aneurysmal* / diagnostic imaging
  • Bone Cysts, Aneurysmal* / pathology
  • Fasciitis* / genetics
  • Fasciitis* / pathology
  • Fibroma*
  • Humans
  • Multimodal Imaging
  • Musculoskeletal Diseases*
  • Proto-Oncogene Proteins / genetics
  • Ubiquitin Thiolesterase / genetics

Substances

  • Ubiquitin Thiolesterase
  • Proto-Oncogene Proteins
  • USP6 protein, human