Ⅱ型神經(jīng)纖維瘤病1例并文獻復(fù)習(xí)

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【中圖分類號】 R739.41；R651 【文獻標(biāo)志碼】 B 【文章編號】 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型神經(jīng)纖維瘤?。╪eurofibromatosistype2，NF2）是一種罕見、可累及全身多個器官、表現(xiàn)為多種腫瘤類型的常染色體顯性遺傳病[1-2]。（剩余7485字）