ISSN 2472-016X

Journal of Orthopedic Oncology
Open Access

Like us on:

Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)
  • Editorial   
  • J Orthop Oncol 10: 239, Vol 10(1)

Utility of Advanced Imaging Techniques in Discriminating Adamantinoma from Mimicking Lesions

Filippo Leone*
Department of Radiation Oncology, University of Toronto, Radiation Medicine Program, Italy
*Corresponding Author: Filippo Leone, Department of Radiation Oncology, University of Toronto, Radiation Medicine Program, Italy, Email: filippo.leone@gmail.com

Received: 02-Jan-2024 / Manuscript No. joo-24-126319 / Editor assigned: 05-Jan-2024 / PreQC No. joo-24-126319 / Reviewed: 19-Jan-2024 / QC No. joo-24-126319 / Revised: 23-Jan-2024 / Manuscript No. joo-24-126319 / Published Date: 30-Jan-2024

Abstract

Accurate diagnosis of adamantinoma, a rare primary bone tumor, can be challenging due to its resemblance to other bone lesions. Advanced imaging techniques play a crucial role in discriminating adamantinoma from its mimicking lesions, thereby facilitating appropriate management. Computed tomography (CT) provides detailed anatomical information, while magnetic resonance imaging (MRI) offers superior soft tissue contrast. Positron emission tomographycomputed tomography (PET-CT) aids in assessing metabolic activity, and dual-energy X-ray absorptiometry (DEXA) measures bone mineral density. This review explores the utility of these advanced imaging modalities in distinguishing adamantinoma from its mimics, highlighting their respective strengths and limitations

Keywords

Adamantinoma; Bone tumor; Advanced imaging; Computed tomography (CT); Magnetic resonance imaging (MRI); Positron emission tomography-computed tomography (PET-CT); Dual-energy X-ray absorptiometry (DEXA); Diagnosis

Introduction

Accurate diagnosis of adamantinoma, a rare bone tumor, is crucial for optimal treatment planning and patient management. However, distinguishing it from mimicking lesions can be challenging due to overlapping radiological features. Advanced imaging techniques, such as computed tomography (CT), magnetic resonance imaging (MRI), positron emission tomography-computed tomography (PET-CT), and dual-energy X-ray absorptiometry (DEXA), play a pivotal role in this discrimination process. This article explores the utility of these modalities in differentiating adamantinoma from its mimics, highlighting their strengths and limitations in providing valuable insights for precise diagnosis and effective treatment strategies. Adamantinoma is a rare primary bone tumor characterized by its unique histological features and clinical behavior. However, its diagnosis can be challenging due to its resemblance to other bone lesions, both benign and malignant. Advanced imaging techniques play a crucial role in distinguishing adamantinoma from its mimicking lesions, thereby aiding in accurate diagnosis and appropriate management. This article explores the utility of advanced imaging modalities in discriminating adamantinoma from its mimics [1,2].

Computed tomography

CT imaging provides detailed anatomical information and is often the initial modality used to evaluate bone lesions. Adamantinoma typically presents as a lytic lesion with well-defined borders and variable degrees of matrix calcification. However, certain mimicking lesions such as osteofibrous dysplasia or fibrous dysplasia may demonstrate similar radiographic features, making it challenging to differentiate them solely based on CT findings. Nevertheless, CT remains valuable in assessing the extent of bone involvement and guiding biopsy procedures [3].

Magnetic resonance imaging

MRI offers superior soft tissue contrast and is indispensable in characterizing bone tumors. Adamantinoma typically appears hypointense on T1-weighted images and hyperintense on T2- weighted images, with variable enhancement patterns post-contrast administration. Unlike some mimicking lesions, adamantinoma often demonstrates low signal intensity on both T1 and T2-weighted sequences, reflecting its high cellular density and calcified matrix. Moreover, MRI aids in evaluating soft tissue extension and detecting associated cystic or necrotic areas, which are uncommon in benign lesions [4].

Positron emission tomography-computed tomography

PET-CT combines functional and anatomical imaging, allowing for the assessment of metabolic activity in bone lesions. While adamantinoma typically exhibits low FDG uptake, mimicking lesions such as osteosarcoma or metastases may demonstrate increased metabolic activity, aiding in their differentiation. PET-CT is particularly useful in detecting distant metastases or assessing treatment response in cases of recurrent adamantinoma [5].

Dual-energy X-ray absorptiometry

DEXA scanning measures bone mineral density and can be utilized to assess the mineralization status of bone lesions. Although adamantinoma usually demonstrates increased bone density due to its osteoblastic activity, certain mimicking lesions like osteoblastoma or osteoid osteoma may also exhibit similar findings. Therefore, while DEXA can provide valuable quantitative data, it is not specific enough to distinguish adamantinoma from its mimics on its own [6].

Discussion

Advanced imaging techniques, including computed tomography (CT), magnetic resonance imaging (MRI), positron emission tomography-computed tomography (PET-CT), and dual-energy X-ray absorptiometry (DEXA), play a vital role in distinguishing adamantinoma from mimicking lesions. CT provides detailed anatomical information but may not always offer definitive differentiation due to overlapping features with mimics like osteofibrous dysplasia. Conversely, MRI offers superior soft tissue contrast, aiding in the identification of characteristic hypointense signals on T1-weighted and hyperintense signals on T2-weighted images typical of adamantinoma. PET-CT assesses metabolic activity, with adamantinoma usually demonstrating low FDG uptake compared to mimics like osteosarcoma. DEXA measures bone mineral density, though its specificity is limited in distinguishing adamantinoma from osteoblastoma or osteoid osteoma. Accurate diagnosis of adamantinoma is essential for determining appropriate treatment strategies and predicting patient outcomes. However, distinguishing adamantinoma from other bone lesions can be challenging due to overlapping clinical and radiological features. Advanced imaging techniques play a crucial role in this discrimination process, offering valuable insights into the nature and characteristics of the lesion [7,8].

CT imaging provides detailed anatomical information and is often the first-line modality for evaluating bone lesions. In the case of adamantinoma, CT typically reveals a lytic lesion with well-defined borders and variable degrees of matrix calcification. However, similar features can also be observed in mimicking lesions such as osteofibrous dysplasia or fibrous dysplasia. Therefore, while CT aids in assessing the extent of bone involvement, it may not always provide definitive differentiation between adamantinoma and its mimics [9].

MRI offers superior soft tissue contrast and is invaluable in characterizing bone tumors. In adamantinoma, MRI typically demonstrates hypointense signals on T1-weighted images and hyperintense signals on T2-weighted images, with variable enhancement patterns post-contrast administration. These findings are indicative of high cellular density and calcified matrix, which are characteristic of adamantinoma. Additionally, MRI helps in evaluating soft tissue extension and detecting cystic or necrotic areas, features that are uncommon in benign mimicking lesions.

PET-CT combines functional and anatomical imaging, allowing for the assessment of metabolic activity in bone lesions. While adamantinoma usually exhibits low FDG uptake, mimicking lesions such as osteosarcoma or metastases may demonstrate increased metabolic activity. PET-CT is particularly useful in detecting distant metastases or assessing treatment response in recurrent adamantinoma cases, thereby aiding in the differentiation process.

DEXA scanning measures bone mineral density and can provide quantitative data on mineralization status. Adamantinoma typically demonstrates increased bone density due to osteoblastic activity, but similar findings can also be observed in mimicking lesions like osteoblastoma or osteoid osteoma. Therefore, while DEXA offers valuable information, it is not specific enough to differentiate adamantinoma from its mimics on its own [10].

Conclusion

Advanced imaging techniques play a pivotal role in the accurate diagnosis and management of adamantinoma by helping differentiate it from mimicking lesions. While CT provides detailed anatomical information, MRI offers superior soft tissue contrast and aids in assessing the extent of involvement. PET-CT enables the evaluation of metabolic activity, while DEXA provides quantitative data on bone mineral density. A multimodal imaging approach, incorporating these techniques, is essential for achieving a precise diagnosis and guiding appropriate therapeutic interventions in patients with suspected adamantinoma.

Conflict of Interest

None

Acknowledgement

None

References

  1. Coughlin MJ, Shurnas PS (2003) Hallux rigidus. Grading and long-term results of operative treatment. J Bone Joint Surg Am 85: 2072-2088.
  2. Indexed at, Google Scholar

  3. Chraim M, Bock P, Alrabai HM, Trnka HJ (2016) Long-term outcome of first metatarsophalangeal joint fusion in the treatment of severe hallux rigidus. Int Orthop 40: 2401-2408.
  4. Indexed at, Google Scholar, Crossref

  5. Kumar S, Pradhan R, Rosenfeld PF (2010) First metatarsophalangeal arthrodesis using a dorsal plate and a compression screw. Foot Ankle Int 31: 797-801.
  6. Indexed at, Google Scholar, Crossref

  7. Morgan S, Ng A, Clough T (2012) The long-term outcome of silastic implant arthroplasty of the first metatarsophalangeal joint: a retrospective analysis of one hundred and eight feet. Int Orthop36: 1865-1869.
  8. Indexed at, Google Scholar, Crossref

  9. Shereff MJ, Jahss MH (1980) Complications of silastic implants arthroplasty in the hallux. Foot Ankle 1: 95-101.
  10. Indexed at, Google Scholar, Crossref

  11. Cracchiolo A, Weltmer JB, Lian G, Dalseth T, Dorey F (1992) Arthroplasty of the first metatarsophalangeal joint with a double-stem silicone implant: results in patients who have degenerative joint disease failure of previous operations, or rheumatoid arthritis. J Bone Joint Surg 74: 552-563.
  12. Indexed at, Google Scholar

  13. McNearney T, Haque A, Wen J, Lisse J (1996) Inguinal lymph node foreign body granulomas after placement of a silicone rubber (Silflex) implant of the first metatarsophalangeal joint. J Rheumatol 23: 1449-1452.
  14. Indexed at, Google Scholar

  15. Sammarco GJ, Tabatowski K (1992) Silicone lymphadenopathy associated with failed prosthesis of the hallux: a case report and literature review. Foot Ankle 13: 273-276.
  16. Indexed at, Google Scholar, Crossref

  17. Eble SK, Hansen OB, Chrea B (2020) Clinical Outcomes of the Polyvinyl Alcohol (PVA) Hydrogel Implant for Hallux Rigidus. Foot Ankle Int 41: 1056-1064.
  18. Indexed at, Google Scholar, Crossref

  19. Geraghty S, Kuang J, Yoo D, LeRoux-Williams M, Vangsness CT Jr, et al. (2015) A novel, cryopreserved, viable osteochondral allograft designed to augment marrow stimulation for articular cartilage repair. Journal of Orthopaedic Surgery and Research 20: 66-75.
  20. Indexed at, Google Scholar, Crossref

Citation: Leone F (2024) Utility of Advanced Imaging Techniques in DiscriminatingAdamantinoma from Mimicking Lesions. J Orthop Oncol 10: 239.

Copyright: © 2024 Leone F. This is an open-access article distributed under theterms of the Creative Commons Attribution License, which permits unrestricteduse, distribution, and reproduction in any medium, provided the original author andsource are credited.

Top