Co-existing of craniofacial fibrous dysplasia and cerebrovascular diseases: a series of 22 cases and review of the literature

Abstract Background Craniofacial fibrous dysplasia is a fairly rare condition. Some literature have reported a few patients with craniofacial fibrous dysplasia suffering from vascular abnormalities. This study aimed to describe the possible coexistence of craniofacial fibrous dysplasia and cerebrova...

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Autores principales:	Xiaowen Song, Zhi Li
Formato:	article
Lenguaje:	EN
Publicado:	BMC 2021
Materias:	Fibrous dysplasia Cerebrovascular diseases Coexistence Interaction Medicine R
Acceso en línea:	https://doaj.org/article/ab6b37ab226d49048f7f4cf95b60325e
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spelling	oai:doaj.org-article:ab6b37ab226d49048f7f4cf95b60325e2021-11-08T10:57:07ZCo-existing of craniofacial fibrous dysplasia and cerebrovascular diseases: a series of 22 cases and review of the literature10.1186/s13023-021-02102-x1750-1172https://doaj.org/article/ab6b37ab226d49048f7f4cf95b60325e2021-11-01T00:00:00Zhttps://doi.org/10.1186/s13023-021-02102-xhttps://doaj.org/toc/1750-1172Abstract Background Craniofacial fibrous dysplasia is a fairly rare condition. Some literature have reported a few patients with craniofacial fibrous dysplasia suffering from vascular abnormalities. This study aimed to describe the possible coexistence of craniofacial fibrous dysplasia and cerebrovascular diseases for the first time. Method We retrospectively reviewed the 1175 patients with craniofacial fibrous dysplasia in Beijing Tiantan Hospital and the information of the 22 patients coexisted with cerebrovascular diseases were described. In addition, we performed a systematic review for cases of craniofacial fibrous dysplasia with vascular abnormalities. Result 22 out of 1175 patients (1.9%) were diagnosed with craniofacial fibrous dysplasia and cerebrovascular diseases including 9 intracranial aneurysms, 4 venous malformations, 2 arteriovenous malformations, 1 moyamoya disease, 2 intracranial venous stenosis and 4 cerebral ischemia with a mean age of 38.18 years old. Only 2 patients were managed surgically for craniofacial fibrous dysplasia and 6 patients were treated with neurosurgery for cerebrovascular diseases. 8 patients were closely followed and only 1 patient’s symptoms worsened. Conclusion Craniofacial fibrous dysplasia might cause constriction of the intracranial vessels and alteration of the overall hemodynamics of the intracranial vasculature resulting in various cerebrovascular diseases. Multimodal screening and examinations seems reasonable for patients with craniofacial fibrous dysplasia for throughout treatment and prognosis evaluations.Xiaowen SongZhi LiBMCarticleFibrous dysplasiaCerebrovascular diseasesCoexistenceInteractionMedicineRENOrphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-12 (2021)
institution	DOAJ
collection	DOAJ
language	EN
topic	Fibrous dysplasia Cerebrovascular diseases Coexistence Interaction Medicine R
spellingShingle	Fibrous dysplasia Cerebrovascular diseases Coexistence Interaction Medicine R Xiaowen Song Zhi Li Co-existing of craniofacial fibrous dysplasia and cerebrovascular diseases: a series of 22 cases and review of the literature
description	Abstract Background Craniofacial fibrous dysplasia is a fairly rare condition. Some literature have reported a few patients with craniofacial fibrous dysplasia suffering from vascular abnormalities. This study aimed to describe the possible coexistence of craniofacial fibrous dysplasia and cerebrovascular diseases for the first time. Method We retrospectively reviewed the 1175 patients with craniofacial fibrous dysplasia in Beijing Tiantan Hospital and the information of the 22 patients coexisted with cerebrovascular diseases were described. In addition, we performed a systematic review for cases of craniofacial fibrous dysplasia with vascular abnormalities. Result 22 out of 1175 patients (1.9%) were diagnosed with craniofacial fibrous dysplasia and cerebrovascular diseases including 9 intracranial aneurysms, 4 venous malformations, 2 arteriovenous malformations, 1 moyamoya disease, 2 intracranial venous stenosis and 4 cerebral ischemia with a mean age of 38.18 years old. Only 2 patients were managed surgically for craniofacial fibrous dysplasia and 6 patients were treated with neurosurgery for cerebrovascular diseases. 8 patients were closely followed and only 1 patient’s symptoms worsened. Conclusion Craniofacial fibrous dysplasia might cause constriction of the intracranial vessels and alteration of the overall hemodynamics of the intracranial vasculature resulting in various cerebrovascular diseases. Multimodal screening and examinations seems reasonable for patients with craniofacial fibrous dysplasia for throughout treatment and prognosis evaluations.
format	article
author	Xiaowen Song Zhi Li
author_facet	Xiaowen Song Zhi Li
author_sort	Xiaowen Song
title	Co-existing of craniofacial fibrous dysplasia and cerebrovascular diseases: a series of 22 cases and review of the literature
title_short	Co-existing of craniofacial fibrous dysplasia and cerebrovascular diseases: a series of 22 cases and review of the literature
title_full	Co-existing of craniofacial fibrous dysplasia and cerebrovascular diseases: a series of 22 cases and review of the literature
title_fullStr	Co-existing of craniofacial fibrous dysplasia and cerebrovascular diseases: a series of 22 cases and review of the literature
title_full_unstemmed	Co-existing of craniofacial fibrous dysplasia and cerebrovascular diseases: a series of 22 cases and review of the literature
title_sort	co-existing of craniofacial fibrous dysplasia and cerebrovascular diseases: a series of 22 cases and review of the literature
publisher	BMC
publishDate	2021
url	https://doaj.org/article/ab6b37ab226d49048f7f4cf95b60325e
work_keys_str_mv	AT xiaowensong coexistingofcraniofacialfibrousdysplasiaandcerebrovasculardiseasesaseriesof22casesandreviewoftheliterature AT zhili coexistingofcraniofacialfibrousdysplasiaandcerebrovasculardiseasesaseriesof22casesandreviewoftheliterature
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Co-existing of craniofacial fibrous dysplasia and cerebrovascular diseases: a series of 22 cases and review of the literature

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