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Diagnosis of Intraosseous Hibernoma of an Appendicular Skeleton in an Adult – A Rare Case Report

INTRODUCTION: Hibernoma is an uncommon benign tumor composed of multivacuolated brown adipocytes described in the literature a decade back. Intraosseous hibernomas are extremely rare with propensity to affect axial skeleton. Involvement of appendicular skeleton has been reported only twice in the li...

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Autores principales: Srinivasan, Smruti, Rai, Abhishek Kumar, Rahman, Syed Hifzur, Hadole, Bhushan Sunil, Bandebuche, Ajinkya Ramesh, Prabhu, Rudra Mangesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9634395/
https://www.ncbi.nlm.nih.gov/pubmed/36381002
http://dx.doi.org/10.13107/jocr.2022.v12.i04.2758
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author Srinivasan, Smruti
Rai, Abhishek Kumar
Rahman, Syed Hifzur
Hadole, Bhushan Sunil
Bandebuche, Ajinkya Ramesh
Prabhu, Rudra Mangesh
author_facet Srinivasan, Smruti
Rai, Abhishek Kumar
Rahman, Syed Hifzur
Hadole, Bhushan Sunil
Bandebuche, Ajinkya Ramesh
Prabhu, Rudra Mangesh
author_sort Srinivasan, Smruti
collection PubMed
description INTRODUCTION: Hibernoma is an uncommon benign tumor composed of multivacuolated brown adipocytes described in the literature a decade back. Intraosseous hibernomas are extremely rare with propensity to affect axial skeleton. Involvement of appendicular skeleton has been reported only twice in the literature till date. CASE REPORT: We present a case of solitary, painless mass in the left proximal tibia mimicking neoplasm in a 35-year-old male. The plain radiographs revealed a lytic lesion with well-defined margin at the junction of metaphyseal-diaphyseal region of the left proximal tibia. The lesion was hyperintense on T2 and hypointense on T1 with heterogenous enhancement on contrast imaging. FDG-PET showed high uptake of fluorodeoxyglucose. Histopathological examination revealed the presence of multivacuolated cytoplasm with abundant mitochondria suggestive of hibernoma. On immunohistochemistry, the cells were positive for S-100. CONCLUSION: The findings of imaging modalities are non-specific and histopathological examination is required to confirm the diagnosis of hibernoma. Intraosseous hibernoma needs to be considered as a differential diagnosis of sclerotic bone lesion. Further, evaluation with regular follow-up with imaging will be required if the mass undergoes any clinical changes. Both radiologists and pathologists, need to be aware of this rare entity to avoid misdiagnosis of the uncommon lesion.
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spelling pubmed-96343952022-11-14 Diagnosis of Intraosseous Hibernoma of an Appendicular Skeleton in an Adult – A Rare Case Report Srinivasan, Smruti Rai, Abhishek Kumar Rahman, Syed Hifzur Hadole, Bhushan Sunil Bandebuche, Ajinkya Ramesh Prabhu, Rudra Mangesh J Orthop Case Rep Case Report INTRODUCTION: Hibernoma is an uncommon benign tumor composed of multivacuolated brown adipocytes described in the literature a decade back. Intraosseous hibernomas are extremely rare with propensity to affect axial skeleton. Involvement of appendicular skeleton has been reported only twice in the literature till date. CASE REPORT: We present a case of solitary, painless mass in the left proximal tibia mimicking neoplasm in a 35-year-old male. The plain radiographs revealed a lytic lesion with well-defined margin at the junction of metaphyseal-diaphyseal region of the left proximal tibia. The lesion was hyperintense on T2 and hypointense on T1 with heterogenous enhancement on contrast imaging. FDG-PET showed high uptake of fluorodeoxyglucose. Histopathological examination revealed the presence of multivacuolated cytoplasm with abundant mitochondria suggestive of hibernoma. On immunohistochemistry, the cells were positive for S-100. CONCLUSION: The findings of imaging modalities are non-specific and histopathological examination is required to confirm the diagnosis of hibernoma. Intraosseous hibernoma needs to be considered as a differential diagnosis of sclerotic bone lesion. Further, evaluation with regular follow-up with imaging will be required if the mass undergoes any clinical changes. Both radiologists and pathologists, need to be aware of this rare entity to avoid misdiagnosis of the uncommon lesion. Indian Orthopaedic Research Group 2022-04 2022-04 /pmc/articles/PMC9634395/ /pubmed/36381002 http://dx.doi.org/10.13107/jocr.2022.v12.i04.2758 Text en Copyright: © Indian Orthopaedic Research Group https://creativecommons.org/licenses/by-nc-sa/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Srinivasan, Smruti
Rai, Abhishek Kumar
Rahman, Syed Hifzur
Hadole, Bhushan Sunil
Bandebuche, Ajinkya Ramesh
Prabhu, Rudra Mangesh
Diagnosis of Intraosseous Hibernoma of an Appendicular Skeleton in an Adult – A Rare Case Report
title Diagnosis of Intraosseous Hibernoma of an Appendicular Skeleton in an Adult – A Rare Case Report
title_full Diagnosis of Intraosseous Hibernoma of an Appendicular Skeleton in an Adult – A Rare Case Report
title_fullStr Diagnosis of Intraosseous Hibernoma of an Appendicular Skeleton in an Adult – A Rare Case Report
title_full_unstemmed Diagnosis of Intraosseous Hibernoma of an Appendicular Skeleton in an Adult – A Rare Case Report
title_short Diagnosis of Intraosseous Hibernoma of an Appendicular Skeleton in an Adult – A Rare Case Report
title_sort diagnosis of intraosseous hibernoma of an appendicular skeleton in an adult – a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9634395/
https://www.ncbi.nlm.nih.gov/pubmed/36381002
http://dx.doi.org/10.13107/jocr.2022.v12.i04.2758
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