结论孤立性纤维瘤是一种少见疾病，必须结合既往病史、临床症状、各种影像学资料综合分析，才有可能作出准确的诊断。
Conclusion SFT is a rare disease. its accurate diagnosis needs an overall analysis combined with medical history clinical symptoms and various imaging data.
蝶骨翼发育不良可以是一个孤立性的发现，也可以见于神经纤维瘤病I型患者。
Sphenoid wing dysplasia can occur as an isolated finding or in patients who have Neurofibromatosis type 1. Approximately 50% of cases are associated with neurofibromatosis type 1.
蝶骨翼发育不良可以是一个孤立性的发现，也可以见于神经纤维瘤病I型患者。
Sphenoid wing dysplasia can occur as an isolated finding or in patients who have Neurofibromatosis type 1. Approximately 50% of cases are associated with neurofibromatosis type 1.
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