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成人附肢骨骼骨内冬眠瘤的诊断——1例罕见病例报告

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

作者信息

Srinivasan Smruti, Rai Abhishek Kumar, Rahman Syed Hifzur, Hadole Bhushan Sunil, Bandebuche Ajinkya Ramesh, Prabhu Rudra Mangesh

机构信息

Department of General Surgery, Seth GS Medical College and KEM Hospital, Mumbai, Maharashtra. India.

Department of Orthopaedics, Seth GS Medical College and KEM Hospital, Mumbai. Maharashtra. India.

出版信息

J Orthop Case Rep. 2022 Apr;12(4):40-43. doi: 10.13107/jocr.2022.v12.i04.2758.

DOI:10.13107/jocr.2022.v12.i04.2758
PMID:36381002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9634395/
Abstract

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.

摘要

引言

冬眠瘤是一种罕见的良性肿瘤,由多泡状棕色脂肪细胞组成,早在十年前就有文献记载。骨内冬眠瘤极为罕见,倾向于累及中轴骨骼。迄今为止,文献中仅报道过两例累及四肢骨骼的病例。

病例报告

我们报告一例35岁男性,左胫骨近端出现一个类似肿瘤的孤立性无痛肿块。X线平片显示左胫骨近端干骺端-骨干交界处有一个边界清晰的溶骨性病变。该病变在T2加权像上呈高信号,在T1加权像上呈低信号,增强扫描呈不均匀强化。氟代脱氧葡萄糖正电子发射断层扫描(FDG-PET)显示氟代脱氧葡萄糖摄取增高。组织病理学检查显示存在多泡状细胞质,线粒体丰富,提示为冬眠瘤。免疫组织化学检查显示细胞S-100阳性。

结论

影像学检查结果无特异性,需要组织病理学检查来确诊冬眠瘤。骨内冬眠瘤需要作为硬化性骨病变的鉴别诊断之一。此外,如果肿块出现任何临床变化,需要定期进行影像学随访评估。放射科医生和病理科医生都需要了解这种罕见疾病,以避免误诊这种不常见的病变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da05/9634395/7ae5493d7b1a/JOCR-12-40-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da05/9634395/3ce2c07db9f4/JOCR-12-40-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da05/9634395/ba37b175099e/JOCR-12-40-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da05/9634395/592d3e6b7c05/JOCR-12-40-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da05/9634395/9811c4b31c7c/JOCR-12-40-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da05/9634395/7ae5493d7b1a/JOCR-12-40-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da05/9634395/3ce2c07db9f4/JOCR-12-40-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da05/9634395/ba37b175099e/JOCR-12-40-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da05/9634395/592d3e6b7c05/JOCR-12-40-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da05/9634395/9811c4b31c7c/JOCR-12-40-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da05/9634395/7ae5493d7b1a/JOCR-12-40-g005.jpg

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Intraosseous hibernoma: case report and tumor characterization.骨内冬眠瘤:病例报告及肿瘤特征分析
BJR Case Rep. 2015 Jul 29;1(3):20150204. doi: 10.1259/bjrcr.20150204. eCollection 2015.
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Intraosseous Lipoma: 18 Years of Experience at a Single Institution.骨内脂肪瘤:单一机构18年的经验
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