Background: No information is currently available regarding the natural history of asymptomatic intracranial aneurysms in beta-thalassemia, raising several concerns about their proper management. Methods: We performed a prospective longitudinal three-year-long MR-angiography study on nine beta-thalassemia patients (mean-age 40.3 ± 7.5, six females, 8 transfusion dependent) harboring ten asymptomatic intracranial aneurysms. In addition, we analyzed the clinical files of all adult beta-thalassemia patients (160 patients including those followed with MR-angiography, 121 transfusion dependent) referring to our Centers between 2014 and 2019 searching for history of subarachnoid hemorrhage or history of symptomatic intracranial aneurysms. Results: At the end of the three-year-long follow-up, no patient showed any change in the size and shape of the aneurysms, none presented new intracranial aneurysms or artery stenoses, none showed new brain vascular-like parenchymal lesions or enlargement of the preexisting ones. Besides, in our database of all adult beta-thalassemia patients, no one had history of subarachnoid hemorrhage or history of symptomatic intracranial aneurysms. Conclusions: Incidental asymptomatic intracranial aneurysms do not seem to be associated, in beta-thalassemia, with an increased risk of complications (enlargement or rupture) at least in the short term period, helping to optimize human and economic resources and patient compliance during their complex long-lasting management.

Asymptomatic intracranial aneurysms in beta-thalassemia: A three-year follow-up report / Manara, R.; Caiazza, M.; Di Concilio, R.; Ciancio, A.; De Michele, E.; Maietta, C.; Capalbo, D.; Russo, C.; Roberti, D.; Casale, M.; Elefante, A.; Esposito, F.; Ponticorvo, S.; Russo, A. G.; Canna, A.; Cirillo, M.; Perrotta, S.; Tartaglione, I.. - In: ORPHANET JOURNAL OF RARE DISEASES. - ISSN 1750-1172. - 15:1(2020), p. 21. [10.1186/s13023-020-1302-3]

Asymptomatic intracranial aneurysms in beta-thalassemia: A three-year follow-up report

Capalbo D.;Russo C.;Casale M.;Elefante A.;Canna A.;
2020

Abstract

Background: No information is currently available regarding the natural history of asymptomatic intracranial aneurysms in beta-thalassemia, raising several concerns about their proper management. Methods: We performed a prospective longitudinal three-year-long MR-angiography study on nine beta-thalassemia patients (mean-age 40.3 ± 7.5, six females, 8 transfusion dependent) harboring ten asymptomatic intracranial aneurysms. In addition, we analyzed the clinical files of all adult beta-thalassemia patients (160 patients including those followed with MR-angiography, 121 transfusion dependent) referring to our Centers between 2014 and 2019 searching for history of subarachnoid hemorrhage or history of symptomatic intracranial aneurysms. Results: At the end of the three-year-long follow-up, no patient showed any change in the size and shape of the aneurysms, none presented new intracranial aneurysms or artery stenoses, none showed new brain vascular-like parenchymal lesions or enlargement of the preexisting ones. Besides, in our database of all adult beta-thalassemia patients, no one had history of subarachnoid hemorrhage or history of symptomatic intracranial aneurysms. Conclusions: Incidental asymptomatic intracranial aneurysms do not seem to be associated, in beta-thalassemia, with an increased risk of complications (enlargement or rupture) at least in the short term period, helping to optimize human and economic resources and patient compliance during their complex long-lasting management.
2020
Asymptomatic intracranial aneurysms in beta-thalassemia: A three-year follow-up report / Manara, R.; Caiazza, M.; Di Concilio, R.; Ciancio, A.; De Michele, E.; Maietta, C.; Capalbo, D.; Russo, C.; Roberti, D.; Casale, M.; Elefante, A.; Esposito, F.; Ponticorvo, S.; Russo, A. G.; Canna, A.; Cirillo, M.; Perrotta, S.; Tartaglione, I.. - In: ORPHANET JOURNAL OF RARE DISEASES. - ISSN 1750-1172. - 15:1(2020), p. 21. [10.1186/s13023-020-1302-3]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/819682
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