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Title: Cerebral arterio-venous malformations hemodynamics changes in hereditary hemorrhagic telangiectasia - case report. Author: Haettel P, Devalckeneer A, Bretzner M, Bourgeois P, Lejeune JP, Reyns N, Aboukais R. Journal: Neurochirurgie; 2022 Dec; 68(6):e101-e103. PubMed ID: 35934538. Abstract: BACKGROUND: Spontaneous obliteration of cerebral arteriovenous malformations (AVMs) is a rare phenomenon. Hereditary Hemorrhagic Telangiectasia (HHT) is a predisposal genetic condition for AVMs development in all organs. CASE ILLUSTRATION: We report the case of a 34 years old woman with HHT family history. After radiosurgical treatment of a symptomatic evolving cerebellar AVM, late control subtracted digital angiography (DSA) demonstrated the complete obliteration of this AVM but also spontaneous obliteration of 3 fronto-parietal AVMs without any hemorrhagic sign on MRI. CONCLUSION: To our knowledge, this is the first report of spontaneous obliteration of multiple and unruptured AVMs in a HTT case.[Abstract] [Full Text] [Related] [New Search]