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Int J Surg Pathol ; 32(3): 511-514, 2024 May.
Article in English | MEDLINE | ID: mdl-37487199

ABSTRACT

Concurrent occurrence of schwannoma and meningiomas are rare, and are found especially in association with neurofibromatosis type 2 (NF2). Occurrence of mixed tumor without the aforementioned conditions is extremely rare. We present three cases of mixed tumor in different locations, including two with NF2 and one without NF2. We analyse the relationship of mixed tumor with NF2 and its clinical implications. Presence of mixed schwannoma-meningioma should prompt screening for NF2. Thus aids in early diagnosis of unsuspected NF2 cases. We observed that irrespective of different locations, cases with NF2 showed frequent recurrence of schwannoma as compared to case who did not fit in the existing clinical criteria for NF2. Collision tumor and thereby NF2 mutations indicates the prognosis and recurrence of the tumor, thereby guides in deciding the management.


Subject(s)
Meningeal Neoplasms , Meningioma , Myoepithelioma , Neurilemmoma , Neurofibromatosis 2 , Humans , Neurofibromatosis 2/complications , Neurofibromatosis 2/diagnosis , Neurofibromatosis 2/genetics , Meningioma/complications , Meningioma/diagnosis , Meningioma/genetics , Meningeal Neoplasms/complications , Meningeal Neoplasms/diagnosis , Meningeal Neoplasms/genetics , Neurilemmoma/complications , Neurilemmoma/diagnosis , Carcinogenesis , Cell Transformation, Neoplastic
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