TY - JOUR
T1 - Asymptomatic intracranial aneurysms in beta-thalassemia
T2 - A three-year follow-up report
AU - Manara, Renzo
AU - Caiazza, Martina
AU - Di Concilio, Rosanna
AU - Ciancio, Angela
AU - De Michele, Elisa
AU - Maietta, Caterina
AU - Capalbo, Daniela
AU - Russo, Camilla
AU - Roberti, Domenico
AU - Casale, Maddalena
AU - Elefante, Andrea
AU - Esposito, Fabrizio
AU - Ponticorvo, Sara
AU - Russo, Andrea Gerardo
AU - Canna, Antonietta
AU - Cirillo, Mario
AU - Perrotta, Silverio
AU - Tartaglione, Immacolata
N1 - Funding Information:
Financial support was provided by Programma VALERE (VAnviteLli pEr la RicErca), Università della Campania “L. Vanvitelli”, Naples, Italy (SP).
Publisher Copyright:
© 2020 The Author(s).
PY - 2020/1/20
Y1 - 2020/1/20
N2 - 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.
AB - 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.
KW - Aneurysm
KW - Beta-thalassemia
KW - Magnetic resonance angiography
KW - Subarachnoid hemorrhage
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U2 - 10.1186/s13023-020-1302-3
DO - 10.1186/s13023-020-1302-3
M3 - Article
C2 - 31959195
AN - SCOPUS:85078398126
SN - 1750-1172
VL - 15
JO - Orphanet Journal of Rare Diseases
JF - Orphanet Journal of Rare Diseases
IS - 1
M1 - 21
ER -