Histological quantification of lesion growth rate in hyperostosis frontalis interna (HFI).

IF 2.1
Russell Hogg, Tara Peburn
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Abstract

Hyperostosis frontalis interna (HFI) is a human skeletal disease characterized by nodules of hyperplastic bone and thickening of the frontal bone's inner surface. Despite its high prevalence in older adults and well-demonstrated neurological comorbidities, HFI's etiology and pathogenesis are poorly understood, including the growth rates of HFI lesions. This lack of information on the rate of progression has obvious consequences for the development of treatment and prevention protocols. Therefore, the aim of this study is to use histopathologic assessment of HFI lesions to directly quantify the growth rate of bone tissue in HFI. To quantify growth rates within HFI lesions, we prepared histological sections of HFI-affected frontal bone from anonymized human cadaver specimens donated to the Anatomical Board of the State of Florida. We measured lamellar breadths from lesioned as well as unlesioned bone to estimate a daily secretion rate (DSR) for the bone tissue, calibrated using dental enamel growth increments from the same individuals. Our data support a median DSR of ~0.9 μm, yielding a lesion expansion rate of approximately 3 years per millimeter of bone thickness. Comparisons of lesioned and unlesioned bone suggest HFI is not associated with a significantly higher osteoblast secretion rate in lesioned bone. Our data suggest that typical HFI progression is a slow, cumulative process, without any clear evidence of acceleration in the osteoblast secretory rate. The slow progression of HFI provides ample opportunity for early identification and clinical interventions before it progresses to cause neurological deficits.

额内肥厚症(HFI)病变生长速率的组织学定量分析。
额内肥厚症(HFI)是一种人类骨骼疾病,其特征是骨结节增生和额骨内表面增厚。尽管HFI在老年人中发病率很高,并有明显的神经并发症,但HFI的病因和发病机制尚不清楚,包括HFI病变的生长速度。缺乏关于进展速度的信息对治疗和预防方案的制定产生了明显的影响。因此,本研究的目的是利用HFI病变的组织病理学评估来直接量化HFI中骨组织的生长速度。为了量化HFI病变内的生长速度,我们从捐赠给佛罗里达州解剖委员会的匿名人类尸体标本中制备了HFI影响的额骨的组织学切片。我们测量了受损骨和未受损骨的板层宽度,以估计骨组织的日分泌率(DSR),使用来自同一个体的牙釉质生长增量进行校准。我们的数据支持中位DSR为~0.9 μm,每毫米骨厚度的病变扩展率约为3年。病变骨与未病变骨的比较表明,HFI与病变骨中明显较高的成骨细胞分泌率无关。我们的数据表明,典型的HFI进展是一个缓慢的累积过程,没有任何明显的证据表明成骨细胞分泌速度加快。HFI的缓慢进展为早期识别和临床干预提供了充足的机会,防止其发展到导致神经功能障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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