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Hyperostosis Frontalis Interna and a Question on Its Pathology: A Case Report

Patient: Female, 90-year-old Final Diagnosis: Cerebrovascular infarction Symptoms: Unknown symptoms – post-mortem anatomical study Medication:— Clinical Procedure: — Specialty: Anatomy • Neurology OBJECTIVE: Unknown etiology BACKGROUND: Hyperostosis frontalis interna is a boney overgrowth of the inn...

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Detalles Bibliográficos
Autores principales: Stiene, Jennifer Michelle, Frank, Patrick William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575136/
https://www.ncbi.nlm.nih.gov/pubmed/36217295
http://dx.doi.org/10.12659/AJCR.937450
Descripción
Sumario:Patient: Female, 90-year-old Final Diagnosis: Cerebrovascular infarction Symptoms: Unknown symptoms – post-mortem anatomical study Medication:— Clinical Procedure: — Specialty: Anatomy • Neurology OBJECTIVE: Unknown etiology BACKGROUND: Hyperostosis frontalis interna is a boney overgrowth of the inner side of the frontal bone of the skull caused by overgrowth of the endocranial surface. It is most often found in women after menopause. It is also associated with hormonal imbalance, being overweight, history of headaches, and neurocognitive degenerative conditions. Female gender, advanced age, extended estrogen stimulation, and elevated leptin levels may also play a role. The thickening is usually confined to the frontal bone, but it can spread as far as the anterior parietal and temporal bones. CASE REPORT: During a medical school dissection course, an extensive boney overgrowth in the frontal regions covering the inside of the frontal bone of the skull of a 90-year-old female donor, who died of a cerebrovascular infarction, was identified. This boney overgrowth was mainly confined within the frontal region, but there was some boney overgrowth that extended to the temporal bones. The overgrowth in the endocranium of the temporal bone was not as severe as the overgrowth of the frontal bone. The morphology of the overgrowth was rigid, uneven, and bumpy. Based upon the physical characteristics, we concluded that this presentation was consistent with hyperostosis frontalis interna. CONCLUSIONS: Our female donor was found to exhibit a phenomenon which could be clinically underdiagnosed due to its internal nature and asymptomatic presentation. Insight into the potential causes of HFI and its identification during clinical evaluation offers a path for future research to better identify and manage cases of HFI.