Artikel: Hump on head: Rare case of bi-frontal fibrous dysplasia.
Surgical neurology international
2024 Band 15, Seite(n) 1
Abstract: Background: FD is relatively rare in the craniofacial region, accounting for only 20% of all cases. Currently, two general subtypes of FD are recognized: monostotic and polyostotic. The monostotic form is more frequent, accounting for 75% to 80% of ... ...
Abstract | Background: FD is relatively rare in the craniofacial region, accounting for only 20% of all cases. Currently, two general subtypes of FD are recognized: monostotic and polyostotic. The monostotic form is more frequent, accounting for 75% to 80% of fibrous dysplasia cases. Case description: An 18-year-old male presented with the complaint of bony-hard swelling over the forehead for 8 years. Radiology showed an expansile osseous lesion involving frontal bones. The patient underwent bi-frontal craniectomy with gross total resection of tumour mass with titanium mesh cranioplasty. His postoperative period was uneventful and was discharged on the seventh postoperative day. Conclusion: The cases of monostotic skull fibrous dysplasia should be treated by resection of the affected bone and cranioplasty. However, a more conservative re-contouring may be carried out in cases with multifocal involvement or when the excision is considered risky due to proximity to the major venous sinuses. |
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Sprache | Englisch |
Erscheinungsdatum | 2024-01-05 |
Erscheinungsland | United States |
Dokumenttyp | Case Reports |
ISSN | 2229-5097 |
ISSN | 2229-5097 |
DOI | 10.25259/SNI_201_2023 |
Datenquelle | MEDical Literature Analysis and Retrieval System OnLINE |
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