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Hump on head: Rare case of bi-frontal fibrous dysplasia.
Singla, Kunal; Goyal, Nishant; Mittal, Pulkit; Qamer, Zahed Ali; Chaturvedi, Jitender; Kumar, Arvind.
Afiliação
  • Singla K; Department of Neurosurgery, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
  • Goyal N; Department of Neurosurgery, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
  • Mittal P; Department of Neurosurgery, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
  • Qamer ZA; Department of Pathology, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
  • Chaturvedi J; Department of Neurosurgery, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
  • Kumar A; Department of Pathology and Laboratory Medicine, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
Surg Neurol Int ; 15: 1, 2024.
Article em En | MEDLINE | ID: mdl-38344095
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Surg Neurol Int Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Surg Neurol Int Ano de publicação: 2024 Tipo de documento: Article