Bozbuğa Mustafa, Turan Süslü Hikmet
Dr. Lütfi Kirdar Kartal Reseach and Training Hospital, Neurosurgery, Istanbul, Turkey.
Turk Neurosurg. 2009 Apr;19(2):172-6.
An aneurysmal bone cyst (ABC) typically involves the long bones of the extremities, thorax, pelvis, or vertebrae. Skull base involvement is rare. We describe the case of a 9-year-old girl with ABC of the skull base. The patient had presented with nasal obstruction and headache over a period of approximately 8 months. The patient had no history of trauma or surgery. Physical and neurological examination findings normal. Magnetic resonance imaging (MRI) showed a multicystic lesion arising from the sphenoid sinus and extending into ethmoid sinus, superior nasal cavity and medial walls of the orbit. The lesion contained thin internal septations that revealed high signal characteristics on all sequences. The lesion was resected via an extended frontal approach without any complications. Histological evaluation confirmed that the lesion was an ABC. The patient did not receive postoperative radiotherapy. No recurrence was observed after 22 months. ABC should be considered in the differential diagnosis of bone neoplasms in this region.
动脉瘤样骨囊肿(ABC)通常累及四肢长骨、胸部、骨盆或椎骨。颅底受累罕见。我们描述了一名9岁女童颅底ABC的病例。该患者在约8个月的时间里出现鼻塞和头痛。患者无外伤或手术史。体格检查和神经学检查结果正常。磁共振成像(MRI)显示一个多房性病变,起源于蝶窦并延伸至筛窦、鼻腔上部和眶内侧壁。病变内有薄的内部间隔,在所有序列上均显示高信号特征。通过扩大的额部入路切除病变,无任何并发症。组织学评估证实病变为ABC。患者未接受术后放疗。22个月后未观察到复发。在该区域骨肿瘤的鉴别诊断中应考虑ABC。