A Di Rita, F Zerini, A M Buccoliero, V Zanchi, F Giordano, G Spinelli
{"title":"Congenital cranial fasciitis of the ethmoid bone with extensive intracranial and facial involvement: a case report and review of the literature.","authors":"A Di Rita, F Zerini, A M Buccoliero, V Zanchi, F Giordano, G Spinelli","doi":"10.1016/j.ijom.2025.03.009","DOIUrl":null,"url":null,"abstract":"<p><p>Cranial fasciitis is a rare fibroproliferative condition predominantly affecting children. An unusual case of cranial fasciitis in a full-term male newborn presenting with significant right malar swelling is reported. Initial imaging revealed a large frontal extra-axial mass displacing both frontal lobes and extending to the right infratemporal fossa and orbit, subsequently diagnosed via a transoral biopsy. Two-stage surgery involving a multidisciplinary team was performed to completely remove both the intracranial and extracranial components of the lesion. Long-term follow-up MRI indicated no recurrence of the disease at 16 months post-resection. Multidisciplinary collaboration is crucial in managing complex craniofacial conditions, especially in newborns and infants.</p>","PeriodicalId":94053,"journal":{"name":"International journal of oral and maxillofacial surgery","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of oral and maxillofacial surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.ijom.2025.03.009","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Cranial fasciitis is a rare fibroproliferative condition predominantly affecting children. An unusual case of cranial fasciitis in a full-term male newborn presenting with significant right malar swelling is reported. Initial imaging revealed a large frontal extra-axial mass displacing both frontal lobes and extending to the right infratemporal fossa and orbit, subsequently diagnosed via a transoral biopsy. Two-stage surgery involving a multidisciplinary team was performed to completely remove both the intracranial and extracranial components of the lesion. Long-term follow-up MRI indicated no recurrence of the disease at 16 months post-resection. Multidisciplinary collaboration is crucial in managing complex craniofacial conditions, especially in newborns and infants.