Multiple cerebral cavernous malformations

Case contributed by James Harvey
Diagnosis certain

Presentation

Seizures since infancy. Presented to ED following a prolonged seizure.

Patient Data

Age: 20 years
Gender: Female
This study is a stack
Axial
non-contrast
This study is a stack
Coronal C+
delayed
This study is a stack
non-contrast
This study is a stack
Axial C+
delayed
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Info

Several dense calcified lesions are seen. A well-circumscribed lesion involves the cingulate gyrus and body of the corpus callosum.
Scattered calcification is also seen within the right frontal lobe with surrounding hyopdensity. 

There is no enhancement on the post-contrast study.

MRI brain

mri
This study is a stack
Axial
SWI
This study is a stack
Axial
T2
This study is a stack
Axial
T1
This study is a stack
Axial
FLAIR
This study is a stack
Axial
ADC
This study is a stack
Axial
DWI
This study is a stack
Axial
T1 C+
This study is a stack
Sagittal
T1 C+
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Info

Multiple areas of SWI blooming artefact representing cavernous malformations are seen within the supra and infratentorial brain parenchyma. The largest one in the right frontal region is heterogeneous with predominant hyperintense foci involving the grey and white matter.  Blooming artefacts noted within in keeping with blood products.
The adjacent grey and white matter shows atrophy.  Ipsilateral mild dilatation of the frontal horn of the lateral ventricle is likely related to gliosis.  

Numerous other cavernous malformations are seen.

There is no significant perilesional edema. No mass effect or midline shift.  

Case Discussion

Cavernous malformations are usually isolated. Where multiple cavernous malformations are present, familial multiple cavernous malformation syndrome must be considered. This condition typically presents with seizures. The inheritance pattern is autosomal dominant, with variable penetrance.

This patient had undergone previous surgical evacuation of hemorrhage within the right frontal lobe.

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