Fibrous dysplasia and aneurysmal bone cyst of the skull base presenting with blindness: a report of a rare locally aggressive example.

Abdullah Sulieman Terkawi, Khalid H Al-Qahtani, Eman Baksh, Lahbib Soualmi, Asim El-Bagir Mohamed, Abdulrahman J Sabbagh
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引用次数: 24

Abstract

Fibrous dysplasia (FD) and aneurysmal bone cyst (ABC) are uncommon benign intraosseous lesions. Simultaneous occurrence of both lesions is extremely rare. We present an example of concomitant FD and ABC in a 7 year-old with left eye blindness and discharge of one month duration. Physical examination revealed a proptotic left eye and bulging of the hard palate. CT and MRI are consistent with FD and ABC that involved the sphenoid and ethmoidal bones bilaterally. Incomplete combined endonasalcranial resection was performed. The patient presented five months postoperatively with a large recurrence and subsequent follow up was lost. Concomitant FD with ABC may occur in paranasal sinuses and may develop rapidly and exhibit locally aggressive behavior.

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以失明为表现的颅底纤维发育不良及动脉瘤性骨囊肿:一例罕见的局部侵袭性病例报告。
纤维性发育不良(FD)和动脉瘤性骨囊肿(ABC)是罕见的良性骨内病变。两种病变同时发生是极为罕见的。我们报告一例伴发FD和ABC的7岁患儿,左眼失明,出血持续一个月。体格检查发现左眼突出,硬腭突出。CT和MRI显示FD和ABC均累及双侧蝶骨和筛骨。不完全联合颅内腔切除术。患者术后5个月出现大面积复发,随后失去随访。伴随FD与ABC可发生在鼻窦,可迅速发展并表现出局部侵袭性行为。
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