Intraosseous hibernoma: clinicopathologic and imaging analysis of 18 cases

Author:

Gangahar Chiraag N1,Dehner Carina A1,Wang David P2,Amini Behrang3,Hillen Travis4,O'Conor Christopher5,Jennings Sydney N6,Byrnes Kathleen1,Montgomery Elizabeth A7,Czerniak Bogdan A2,Bridge Julia A89,Schroeder Molly C1,Jennings Jack W4,Wang Wei‐Lien2,Chrisinger John S A1ORCID

Affiliation:

1. Department of Pathology and Immunology Washington University School of Medicine St Louis MO USA

2. Department of Pathology University of Texas MD Anderson Cancer Center Houston TX USA

3. Department of Diagnostic Imaging University of Texas MD Anderson Cancer Center Houston TX USA

4. Musculoskeletal Section, Department of Radiology Mallinckrodt Institute of Radiology, Washington University School of Medicine St Louis MO USA

5. Department of Pathology, Microbiology, and Immunology Vanderbilt University Medical Center Nashville TN USA

6. Washington University St. Louis MO USA

7. Department of Pathology and Laboratory Medicine University of Miami Miami FL USA

8. Propath Dallas TX USA

9. Department of Pathology and Microbiology University of Nebraska Medical Center Omaha NE USA

Abstract

AimsIntraosseous hibernomas are rarely reported tumours with brown adipocytic differentiation of unknown aetiology, with only 38 cases documented in the literature. We sought to further characterise the clinicopathologic, imaging and molecular features of these tumours.Methods and resultEighteen cases were identified occurring in eight females and 10 males (median age = 65 years, range = 7–75). Imaging indication was cancer surveillance/staging in 11 patients and clinical concern for a metastasis was raised in 13 patients. The innominate bone (7), sacrum (5), mobile spine (4), humerus (1) and femur (1) were involved. Median tumour size was 1.5 cm (range = 0.8–3.8). Tumours were sclerotic (11), mixed sclerotic and lytic (4) or occult (1). Microscopically, tumours were composed of large polygonal cells with distinct cell membranes, finely vacuolated cytoplasm, central or paracentral small bland nuclei with prominent scalloping. Growth around trabecular bone was observed. Tumour cells were immunoreactive for S100 protein (15/15) and adipophilin (5/5), while negative for keratin AE1/AE3(/PCK26) (0/14) and brachyury (0/2). Chromosomal microarray analysis, performed on four cases, did not show clinically significant copy number variation across the genome or on 11q, the site of AIP and MEN1.ConclusionAnalysis of 18 cases of intraosseous hibernoma, to our knowledge, the largest series to date, revealed that these tumours are most often detected in the spine and pelvis of older adults. Tumours were generally small, sclerotic and frequently found incidentally and can raise concern for metastasis. Whether or not these tumours are related to soft tissue hibernomas is uncertain.

Publisher

Wiley

Subject

General Medicine,Histology,Pathology and Forensic Medicine

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Lipomatoses;Annales d'Endocrinologie;2024-06

2. Imaging diagnosis: CT characteristics of a retrobulbar hibernoma in a dog;Veterinary Radiology & Ultrasound;2024-01-31

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