Hump on head: Rare case of bi-frontal fibrous dysplasia

Kunal Singla, Nishant Goyal, Pulkit Mittal, Zahed Ali Qamer, Jitender Chaturvedi, Arvind Kumar
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引用次数: 0

Abstract

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. 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. 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.
头部有驼峰双额纤维发育不良的罕见病例
FD 在颅面区域相对罕见,仅占所有病例的 20%。目前,纤维性发育不良一般有两种亚型:单恒定型和多恒定型。单发型更常见,占纤维发育不良病例的 75% 至 80%。一名 18 岁的男性主诉前额骨质硬性肿胀 8 年。放射学检查显示,患者的额骨有扩张性骨质病变。患者接受了双额颅骨切除术,对肿瘤块进行了全切,并进行了钛网开颅成形术。患者术后恢复顺利,术后第七天出院。然而,对于多灶性受累的病例,或者由于靠近主要静脉窦而认为切除手术有风险的病例,可以采取更为保守的重新整形手术。
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