Cerebral malaria

Changed by Owen Kang, 24 Mar 2018

Updates to Article Attributes

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Cerebral malaria is a rare intracranial complication of a malarial infection.

Epidemiology

Cerebral malaria is mainly encountered in young children and adults living or travelling in malaria-endemic areas. It is estimated to occur in ~2% of patients with acute Plasmodium falciparum infection, the most common species of Plasmodium that causes malaria.

Clinical presentation

Cerebral malaria should be suspected when there are neurological symptoms on a background of malarial infection. Clinical presentations include: headache, altered state of consciousness, seizures, backache, vomiting, nausea, etc.

Pathology

It can at times be characterised by diffuse petechial haemorrhages on postmortem pathological specimens which are often difficult to identify retrospectively on imaging 1,2.

The haemorrhages are thought to occur when cerebral capillaries and small veins are occluded by sequestered Plasmodium-infected erythrocytes. Hence, this pathological process may lead to areas of infarction.

Radiographic features

Imaging features on its own are often nonspecific correlation with travel history or exposure in an endemic area is mandatory 7. Most published articles are based on case reports and small case series.

The most common findings are related to ischemia involving: deep white matter, cortex, basal ganglia, thalami and cerebellum. These areas of ischemia can be haemorrhagic 6.

CT

CT findings do not appear to not correlate with the degree of parasitaemia and can sometimes be normal 1. However, reported features include 1:

  • cerebral oedema
  • thalamic hypoattenuation from infarcts
  • cerebellar white matter hypoattenuation from infarcts
MRI

Described features include:

  • T2/FLAIR: nonspecific hyperintensities located in the bilateral periventricular white matter, corpus callosum, occipital subcortex, and/or bilateral thalamic regions 3,8
  • DWI: high diffusion signal if cortical infarcts are present
  • SWI: regions of hypointensity representing either petechial microbleeds or regions of haemorrhage in infarcted tissue 6

Treatment and prognosis

Treatment is with parentralparenteral artemisinin derivatives and electrolyte correction, usually in the setting of an intensive care unit, as well as symptomatic treatment (e.g. use of antiepileptic medications) 9.

It is often associated with a high mortality rate (20-50%). However, those patients who survive often have a full recovery with minimal or no long-term sequelae.

  • -</ul><h4>Treatment and prognosis</h4><p>Treatment is with parentral artemisinin derivatives and electrolyte correction, usually in the setting of an intensive care unit, as well as symptomatic treatment (e.g. use of antiepileptic medications) <sup>9</sup>.</p><p>It is often associated with a high mortality rate (20-50%). However, those patients who survive often have a full recovery with minimal or no long-term sequelae.</p>
  • +</ul><h4>Treatment and prognosis</h4><p>Treatment is with parenteral artemisinin derivatives and electrolyte correction, usually in the setting of an intensive care unit, as well as symptomatic treatment (e.g. use of antiepileptic medications) <sup>9</sup>.</p><p>It is often associated with a high mortality rate (20-50%). However, those patients who survive often have a full recovery with minimal or no long-term sequelae.</p>

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