ruptured berry aneurysm

Rupture of a berry aneurysm, also known as a saccular aneurysm, usually results in a subarachnoid hemorrhage (SAH) but can, depending on the location of the rupture and presence of adhesions to the aneurysm, also result in cerebral hematoma, subdural hematoma and/or intraventricular hemorrhage.

Epidemiology

Berry aneurysms form 97% of all aneurysms of the central nervous system. Up to 80% of patients with a spontaneous subarachnoid hemorrhage have ruptured an aneurysm and 90% of these aneurysms are located in the anterior circulation (carotid system), with 10% are found in the posterior circulation (vertebrobasilar system).

Clinical presentation

Rupture of a saccular aneurysm with associated subarachnoid hemorrhage most frequently presents with a sudden, excruciating headache often described as 'the worst I've ever had' or 'thunderclap', resulting from blood being forced into the subarachnoid space under arterial pressure. Other features include:

• visual changes
• facial pain
• seizures
• autonomic disturbances (nausea/vomiting, chills and palpitations)
• focal neurology (sensory loss, weakness, memory loss, language difficulties) 

Examination findings include meningisms (nuchal rigidity, fever, photophobia), altered consciousness, and other focal neurological signs such as ophthalmoplegia and pupillary abnormalities

Mortality from the first rupture is between 25-50% with repeat bleeding a common complication in survivors. With each recurrent bleed, the prognosis is worsened. In the first few days following a subarachnoid hemorrhage, there is an increased risk of additional ischemic injury from the reactive vasospasm from surrounding vasculature.

Pathology

Although some of the details of the pathophysiology of the formation of a berry aneurysm remain unknown, the vast majority of aneurysms arise at arterial branching points along the circle of Willis . It is likely that the difference in composition of intracranial arteries compared to similarly sized arteries in the rest of the body (e.g. reduced thickness of adventitia) plays a significant role in aneurysm formation and rupture. Additional deficiencies in arterial wall strength (e.g. connective tissue disease or infection) further increase the incidence of aneurysm formation - see below.

Rupture of a berry aneurysm is in most cases spontaneous with no clear precipitant. In approximately one-third of cases associated defined increased intracranial arterial pressure can be surmised by history or examination at the time of presentation (e.g. coital rupture, recreational drugs, childbirth, etc..) .

Etiology

• formation of berry aneurysm:
  • sporadic (most)
    • although a genetic component is likely as incidence in first-degree relatives of affected patients is increased
  • genetic
    • Ehlers-Danlos syndrome type IV, neurofibromatosis type 1, Marfan syndrome, autosomal dominant polycystic kidney disease
  • infection (intracranial mycotic aneurysm), although often not referred to as berry aneurysms

Macroscopic appearance

• an unruptured aneurysm appears as a thin-walled, shiny red outpouching usually measuring a few milimeters to 3 cm in diameter 
• rupture usually occurs at the apex of the sac

Microscopic appearance

• the arterial wall adjacent to the neck of the sac usually shows thickening of the intima and thinning out of the media as the neck is approached
• the sac itself is usually made up of thickened intima with the adventitia of the parent artery surrounding the sac

Radiographic features

Determining the site of rupture

After rupture, the location of the blood or hematoma can help determine the site of the ruptured aneurysm in the majority of cases:

• ACOM: ~35%, septum pellucidum, interhemispheric fissure and intraventricular, inferior frontal lobe (intraparenchymal)
• PCOM: ~35%, Sylvian fissure, medial temporal lobe (intraparenchymal)
• MCA: ~20%, Sylvian fissure and intraventricular, anterior temporal lobe (intraparenchymal)
• basilar artery: ~5%, prepontine cistern
• ICA: Sylvian fissure and intra-ventricular
• pericallosal artery: corpus callosum
• PICA: foramen magnum

An intraparenchymal hematoma adjacent to the ruptured aneurysm is known as a jet hematoma or flame hemorrhage, caused when an aneurysm abuts a lobe and at the time of rupture the pressure of the blood leaving the aneurysm dissects into the brain parenchyma. This often coexists with the presence of subdural haemorrahge from the aneursymal rupture.

Aneurysmal characteristics suggestive of rupture

In cases of subarachnoid hemorrhage with multiple aneurysms, it is often important to identify which aneurysm has bled, as not all aneurysms present can be treated simultaneously. The location of blood, particularly if there is a parenchymal hematoma, is very helpful in identifying the responsible aneurysm. If this is not present or if blood is diffusely within the subarachnoid space, then aneurysm morphology can be helpful:

• largest aneurysm
• length-to-neck ratio >1.6
• increased volume to surface area
• aneurysm angulation
• presence of an apical bleb

Treatment and prognosis

The rupture of an intracranial aneurysm is a medical emergency with a high mortality .  Treatment focuses on managing both the aneurysm and complications of hemorrhage.

The aneurysm needs to be secured, either endovascularly by introduction of coils and/or stents or by surgery with clipping of the aneurysm neck.

Complications that require management include hydrocephalus and vasospasm.

Siehe auch:

• Subarachnoidalblutung
• intraventrikuläre Blutung
• sakkuläre zerebrale Aneurysmata

und weiter:

• aneurysm rupture
• Hirnarterienaneurysma
• MCA aneurysm - with rupture
• ruptured cerebral aneurysm non visible on inital angiography