Organ Histopathological Associations with Hyperostosis Frontalis Interna in Humans

SUMMARY: An increased thickening of the frontal bone by irregular laminar additions on the inner surface just deep to the dura mater have been known in the archaeological and medical record as hyperostosis frontalis interna (HFI). The distribution of this is idiosyncratically restricted to the front...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Beatty,Brian, Putcha,Krishna, Shah,Abhishek, Li,Kevin
Lenguaje:English
Publicado: Sociedad Chilena de Anatomía 2021
Materias:
Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022021000100077
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:scielo:S0717-95022021000100077
record_format dspace
spelling oai:scielo:S0717-950220210001000772021-03-01Organ Histopathological Associations with Hyperostosis Frontalis Interna in HumansBeatty,BrianPutcha,KrishnaShah,AbhishekLi,Kevin Hyperostosis frontalis interna Cranium Bone growth Estradiol Histology SUMMARY: An increased thickening of the frontal bone by irregular laminar additions on the inner surface just deep to the dura mater have been known in the archaeological and medical record as hyperostosis frontalis interna (HFI). The distribution of this is idiosyncratically restricted to the frontal and has no known etiology. The prevalence among post-menopausal females and rarity in males suggests that it is hormonally driven. Here we report histopathological findings of particularly hormonally active organs (pituitaries, gonads and liver) from a geriatric cadaveric sample in which HFI is assessed. HFI was present in 50 % of males (7/14) and 95 % (21/22) of females. All males with HFI had testicular atrophy or had testes absent. Males with HFI category C or D had moderate to severe testicular atrophy. Decreased numbers of interstitial cells (Leydig cells) were present in 83.3 % of males with HFI. All but one female (21/22) from this study exhibited evidence of HFI, and ovarian pathologies were unevenly distributed (fibromas in two) and most exhibited signs of being healthy and post-menopausal. Liver pathologies had opposite patterns between the sexes, with more liver pathologies occurring among males without HFI (particularly passive congestion and bile stasis). The only exceptions were that the one case of liver neoplasia was found in a male with HFI and steotosis was found in two cases with HFI and one case without HFI. In females all cases of liver pathologies (steotosis, hepatitis, passive congestion, fibrosis, and bile stasis) were associated with HFI. It appears that gonadal pathology is most closely associated with HFI in males but not females, suggesting that the role of estradiol in this unusual growth of bone in geriatric humans may be worth investigating further.info:eu-repo/semantics/openAccessSociedad Chilena de AnatomíaInternational Journal of Morphology v.39 n.1 20212021-02-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022021000100077en10.4067/S0717-95022021000100077
institution Scielo Chile
collection Scielo Chile
language English
topic Hyperostosis frontalis interna
Cranium
Bone growth
Estradiol
Histology
spellingShingle Hyperostosis frontalis interna
Cranium
Bone growth
Estradiol
Histology
Beatty,Brian
Putcha,Krishna
Shah,Abhishek
Li,Kevin
Organ Histopathological Associations with Hyperostosis Frontalis Interna in Humans
description SUMMARY: An increased thickening of the frontal bone by irregular laminar additions on the inner surface just deep to the dura mater have been known in the archaeological and medical record as hyperostosis frontalis interna (HFI). The distribution of this is idiosyncratically restricted to the frontal and has no known etiology. The prevalence among post-menopausal females and rarity in males suggests that it is hormonally driven. Here we report histopathological findings of particularly hormonally active organs (pituitaries, gonads and liver) from a geriatric cadaveric sample in which HFI is assessed. HFI was present in 50 % of males (7/14) and 95 % (21/22) of females. All males with HFI had testicular atrophy or had testes absent. Males with HFI category C or D had moderate to severe testicular atrophy. Decreased numbers of interstitial cells (Leydig cells) were present in 83.3 % of males with HFI. All but one female (21/22) from this study exhibited evidence of HFI, and ovarian pathologies were unevenly distributed (fibromas in two) and most exhibited signs of being healthy and post-menopausal. Liver pathologies had opposite patterns between the sexes, with more liver pathologies occurring among males without HFI (particularly passive congestion and bile stasis). The only exceptions were that the one case of liver neoplasia was found in a male with HFI and steotosis was found in two cases with HFI and one case without HFI. In females all cases of liver pathologies (steotosis, hepatitis, passive congestion, fibrosis, and bile stasis) were associated with HFI. It appears that gonadal pathology is most closely associated with HFI in males but not females, suggesting that the role of estradiol in this unusual growth of bone in geriatric humans may be worth investigating further.
author Beatty,Brian
Putcha,Krishna
Shah,Abhishek
Li,Kevin
author_facet Beatty,Brian
Putcha,Krishna
Shah,Abhishek
Li,Kevin
author_sort Beatty,Brian
title Organ Histopathological Associations with Hyperostosis Frontalis Interna in Humans
title_short Organ Histopathological Associations with Hyperostosis Frontalis Interna in Humans
title_full Organ Histopathological Associations with Hyperostosis Frontalis Interna in Humans
title_fullStr Organ Histopathological Associations with Hyperostosis Frontalis Interna in Humans
title_full_unstemmed Organ Histopathological Associations with Hyperostosis Frontalis Interna in Humans
title_sort organ histopathological associations with hyperostosis frontalis interna in humans
publisher Sociedad Chilena de Anatomía
publishDate 2021
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022021000100077
work_keys_str_mv AT beattybrian organhistopathologicalassociationswithhyperostosisfrontalisinternainhumans
AT putchakrishna organhistopathologicalassociationswithhyperostosisfrontalisinternainhumans
AT shahabhishek organhistopathologicalassociationswithhyperostosisfrontalisinternainhumans
AT likevin organhistopathologicalassociationswithhyperostosisfrontalisinternainhumans
_version_ 1718445180267266048