Table 1.

Patient demographics and clinical background

PatientAgeGenderLocation of biopsyCCM typeNo. of lesionsLesion size (mm)Inherited mutationHemorrhageOther symptomsStained withEvidence of clots
27 Pons Sporadic >1 15 × 15 None Yes No Fibrin-fibrinogen and VWF Yes 
48 Pons Sporadic 10 None Yes No Fibrin-fibrinogen and VWF Yes 
55 Frontal lobe Sporadic 15 None Yes No Fibrin-fibrinogen and VWF Yes  
31 Other Familial >10 25 CCM1 Yes L, S, U, V Fraser-Lendrum Yes 
18 Left frontal lobe Familial 2-10 10 CCM2 Yes, twice C, H, S, U, V, vertigo Fraser-Lendrum Yes 
51 Right temporal lobe Familial 2-10  25 CCM1 Yes D, H, S, T, lethargy, V, tinnitus Fraser-Lendrum Yes 
23 Parietal lobe Sporadic 20 None Yes  Fibrin-fibrinogen and VWF Yes 
31 Parieto-occipital lobe Sporadic 20 None Yes Fibrin-fibrinogen and VWF Yes 
66 Temporal lobe Sporadic >1 25 None Yes Fibrin-fibrinogen and VWF Yes 
10 34 Frontal cortex NA NA NA NA NA NA Fibrin-fibrinogen and VWF No 
11 69 Frontal cortex NA NA NA NA NA NA Fibrin-fibrinogen and VWF No 
PatientAgeGenderLocation of biopsyCCM typeNo. of lesionsLesion size (mm)Inherited mutationHemorrhageOther symptomsStained withEvidence of clots
27 Pons Sporadic >1 15 × 15 None Yes No Fibrin-fibrinogen and VWF Yes 
48 Pons Sporadic 10 None Yes No Fibrin-fibrinogen and VWF Yes 
55 Frontal lobe Sporadic 15 None Yes No Fibrin-fibrinogen and VWF Yes  
31 Other Familial >10 25 CCM1 Yes L, S, U, V Fraser-Lendrum Yes 
18 Left frontal lobe Familial 2-10 10 CCM2 Yes, twice C, H, S, U, V, vertigo Fraser-Lendrum Yes 
51 Right temporal lobe Familial 2-10  25 CCM1 Yes D, H, S, T, lethargy, V, tinnitus Fraser-Lendrum Yes 
23 Parietal lobe Sporadic 20 None Yes  Fibrin-fibrinogen and VWF Yes 
31 Parieto-occipital lobe Sporadic 20 None Yes Fibrin-fibrinogen and VWF Yes 
66 Temporal lobe Sporadic >1 25 None Yes Fibrin-fibrinogen and VWF Yes 
10 34 Frontal cortex NA NA NA NA NA NA Fibrin-fibrinogen and VWF No 
11 69 Frontal cortex NA NA NA NA NA NA Fibrin-fibrinogen and VWF No 

Patients 10 and 11 were used as control human brain samples. The criteria for clots were based on the presence of fibrin, polyhedrocytes, or platelets.

C, coordination problems; D, decreased sensation; H, headaches; L, limb weakness; NA, not applicable; S, seizures; T, tingling sensation in extremities; U, understanding and speaking problems; V, vision problems.

Fibrin-positive regions, but absence of large clots.

In brain and skin.

Microbleeding.

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