Pai S Balaji, Harish K, Venkatesh M S, Jermely Deepthi
Department of Neurosurgery, M.S. Ramaiah Medical College, Gokula, Bangalore 560054, India.
Department of Surgical Oncology, M.S. Ramaiah Medical College, Bangalore, India.
BMC Ear Nose Throat Disord. 2005 Mar 11;5:2. doi: 10.1186/1472-6815-5-2.
Osteoid osteoma is a benign bone neoplasm which is seen in the long bones of appendicular skeleton. It is rarely seen in the cranium. Skull base osteoid osteoma is extremely rare and has been anecdotally reported.
The authors report a case of a large osteoid osteoma of the ethmoid with intraorbital and intracranial extension in a 33 year old male patient. He presented with loss of vision in the left eye. The intra-cranial extension was excised through a single burr-hole fronto-orbitotomy. The ethmoid and orbital portions were approached and excised through a Weber-Ferguson incision and inferior orbitotomy. Radical excision of the tumor could thus be achieved through a craniofacial approach.
Although benign and rare, skull base osteoid osteoma can present with neurological deficit due to its mass effect and involvement of vital structures. A multispeciality team approach is advisable in such cases if radical excision is to be achieved. A craniofacial approach made radical single stage excision of this multicompartmental osteoid osteoma possible with an uneventful postoperative period.
骨样骨瘤是一种良性骨肿瘤,多见于四肢骨骼的长骨,在颅骨中很少见。颅底骨样骨瘤极为罕见,仅有零星报道。
作者报告了一例33岁男性患者,患有累及眼眶及颅内的筛骨大型骨样骨瘤。患者表现为左眼视力丧失。通过单孔额眶开颅术切除颅内延伸部分。经Weber-Ferguson切口及眶下开颅术处理并切除筛骨及眼眶部分。通过颅面联合入路可实现肿瘤的根治性切除。
颅底骨样骨瘤虽然为良性且罕见,但因其占位效应及累及重要结构,可导致神经功能缺损。若要实现根治性切除,此类病例建议采用多学科团队协作的方法。颅面联合入路使该多部位骨样骨瘤得以一期根治性切除,术后恢复顺利。