Familial Cerebral Cavernous Malformation in a Filipino Familye

Background of the Study Cerebral cavernous malformation is a type of vascular malformations characterized by the absence of intervening brain parenchyma. Cerebral cavernous malformations are of two forms, sporadic and familial. About 0.4-0.8% of the population are affected as assessed based on MRI findings and postmortem findings. Three genetic mutations have been identified: CCM1, CCM2, CCM3, with an incidence of 40%, 40% and 20% respectively. Clinical Presentation This author presents 5 members diagnosed with FCCM within a Filipino family. A 25-year-old male who was admitted due to progressive generalized headache of 2 years duration wherein multiple brain lesions on MRI were seen. All members of the family became symptomatic before 30 years of age. 4 out of the 5 members underwent surgery. However, molecular genetic testing was not done. Conclusion In patients diagnosed with cerebral cavernous malformations, a thorough clinical and family history is warranted accompanied by MRI-GRE/T2* to help establish final diagnosis. Confirmation with molecular genetic testing should be offered to all members of the family for proper neurological and genetic care.

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Publication Details

Journal
International Journal For Multidisciplinary Research
Published
2024-08-19
DOI
https://doi.org/10.36948/ijfmr.2024.v06i04.26264
Primary Topic
Vascular Malformations Diagnosis and Treatment
Type
article
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article

Familial Cerebral Cavernous Malformation in a Filipino Familye

Maria Veronica Comandao -, Christopher Concepcion -
International Journal For Multidisciplinary Research
Vascular Malformations Diagnosis and Treatment
article

Familial Cerebral Cavernous Malformation in a Filipino Familye

Maria Veronica Comandao -, Christopher Concepcion -
article en

Abstract

Background of the Study Cerebral cavernous malformation is a type of vascular malformations characterized by the absence of intervening brain parenchyma. Cerebral cavernous malformations are of two forms, sporadic and familial. About 0.4-0.8% of the population are affected as assessed based on MRI findings and postmortem findings. Three genetic mutations have been identified: CCM1, CCM2, CCM3, with an incidence of 40%, 40% and 20% respectively. Clinical Presentation This author presents 5 members diagnosed with FCCM within a Filipino family. A 25-year-old male who was admitted due to progressive generalized headache of 2 years duration wherein multiple brain lesions on MRI were seen. All members of the family became symptomatic before 30 years of age. 4 out of the 5 members underwent surgery. However, molecular genetic testing was not done. Conclusion In patients diagnosed with cerebral cavernous malformations, a thorough clinical and family history is warranted accompanied by MRI-GRE/T2* to help establish final diagnosis. Confirmation with molecular genetic testing should be offered to all members of the family for proper neurological and genetic care.

International Journal For Multidisciplinary ResearchVol. 6(4)
University of the East Ramon Magsaysay Memorial Medical Center (PH)
Good health and well-being
Openalex Percentile: Top 79%
Vascular Malformations Diagnosis and Treatment
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Familial Cerebral Cavernous Malformation in a Filipino Familye — Maria Veronica Comandao -, Christopher Concepcion - · International Journal For Multidisciplinary Research (2024) | TGRS Research Map | TGRS