Von-Hippel Lindau (VHL) syndrome with bilateral cerebellar hemangioblastomas and retinal angiomas: A rare presentation.

Abhijit Acharya,Souvagya Panigrahi,A K Mahapatra,Rama Chandra Deo,Satya Bhushan Senapati

International journal of surgery case reports（2023）

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摘要

VHL being a lifelong disease with no cure till date, the patients should be frequently screened for lesions at various potential sites in his/her lifetime so as to provide required intervention at the earliest. Hence, a genetic screening for VHL (VHL tumour suppressor gene), should be performed in cases of hemangioblastoma.

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Hemangioblastoma,Retinal angioma,VHL syndrome,Von-Hippel Lindau disease

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