Ⅱ型神经纤维瘤病1例并文献复习

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【中图分类号】 R739.41；R651 【文献标志码】 B 【文章编号】 1672-7770（2025）02-0233-04

Abstract：ObjectiveTo report acase of neurofibromatosis type2and itstreatment.MethodsTheclinical dataof a patient with neurofibromatosis type2 admited to the Department of Neurosurgery，Nanjing BenQ Hospital in August 2O23wereanalyzed retrospectively，and therelated literatureswere reviewed.ResultsThe patient presented with progressive hearing loss of the left ear，tinnitusand left facial swelling.The imaging examination resultsshowthat multiplescatered lesionsinthepatient’sbody.Thepatient hadagood therapeuticeffect after multiple operations.ConclusionsAs neurofibromatosis type2 isan autosomal dominant genetic disease，early detection，earlytreatmentandregularfolow-upshouldbedoneforthis kindof patients.Themain treatmentforthis disease is surgery，but due totheextensiveinvolvement of tumors，multidisciplinary treatment isultimately required.

Key words：neurofibromatosis type 2；meningioma；acoustic neuroma

Ⅱ型神经纤维瘤病（neurofibromatosistype2，NF2）是一种罕见、可累及全身多个器官、表现为多种肿瘤类型的常染色体显性遗传病[1-2]。（剩余7485字）