Elsevier

Seminars in Roentgenology

Volume 39, Issue 4, October 2004, Pages 465-473
Seminars in Roentgenology

Imaging of neurocysticercosis

https://doi.org/10.1016/j.ro.2004.06.007Get rights and content

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Hosts

For Tenia Solium to become clinically manifested, two hosts are needed to complete its life cycle.1 The initial host is the pig. The larvae migrate preferentially toward muscle and are released into the human gastrointestinal tract when undercooked pork meat is consumed. This results in intestinal teniasis generally at the level of the small bowel. The larva remain attached by the scolex to the intestinal mucosa. As the larvae grow, body segments (proglottids) develop progressively from the

Epidemiology

Although cysticercosis occurs worldwide, it is endemic in Latin America, India, and China where 5 to 25% of the population will be seropositive (this is a gross underestimation because only about 50% of infected patients are seropositive).1, 2, 3 In Latin America, nearly 50% of adults with new onset of seizures will show cysticercal lesions on neuroimaging studies. In Africa, nearly 40% of the population in non-Muslim countries harbors the disease. In India, cysticercosis is the most important

Intraparenchymal cysticercosis

Cysticerci must live in the muscle of the pig for weeks to months to grow and mature.1, 2, 3 The scolex is usually attached to the wall of the cyst that is composed of an eosinophilic cuticular layer, a cellular layer with multiple nuclei, musculature, and a loose reticular layer (this is called the “vesicular” stage). These parasites have little neighboring inflammation consisting of lymphocytic and eosinophilic infiltrates. Cysticerci secrete substances that modulate, complement, and

Criteria for diagnosis and classification

Despite its high incidence, the diagnosis of CNS cysticercosis remains difficult. The clinical manifestations are generally nonspecific and the serologic tests have varying degrees of accuracy. The most widely used laboratory examination is an enzyme-linked immunoabsorbent assay (ELISA) that is based on the use of a crude parasite antigen (IgG).4 As stated before, the rate of false-negatives using this test may be as high as 40%.5 A different method uses a T. Solium specific glycoprotein-based

Inactive form (nodular stage)

In these patients, the parasites are no longer viable or degenerating. There is no active immune response from the host and neuroimaging studies show only the sequela of the disease. The most commonly encountered manifestation is that of multiple, small parenchymal calcifications on CT7 (Fig. 1). The calcifications generally measure between 2 and 10 mm. At this stage of the disease, CT is superior to MRI for visualization of the lesions. A recent report indicates that MRI may show persistent

Differential diagnosis of parenchymal cysticercosis

During the vesicular stage, the lesions may be difficult to distinguish (particularly if solitary) from echinococcus (usually a large solitary cyst in the region of the distribution of the middle cerebral artery), sparganosis (seen in patients from southeast Asia, multiple cystic lesions), coenurosis (a very rare disease caused by the cestode Multiceps multiceps), cystic metastases, and multiple abscesses.2, 1, 12, 13 During the colloidal and granular stages, both solitary and multiple cysts

Ventricles

Approximately 10 to 20% of patients with cysticercosis will be shown to have lesions in the ventricles.2, 17 Symptoms are generally the result of obstruction and hydrocephalus (which may be fatal). Viable lesions are cyst-like and may be difficult to identify on CT. For intraventricular cysticercosis, MR is the imaging method of choice. The cyst contents are generally isointense to CSF on T1- and T2-weighted and FLAIR images (Fig. 5A and B). Occasionally they are slightly brighter than CSF on

Spinal cord

There are two types of cysticercal spinal involvement. The most common involvement is when the parasites are located in the subarachnoid space and the least common involvement is when the cysts are inside of the spinal cord.20 Approximately 5% of patients with cisternal cysticercosis will have disease involving the spinal subarachnoid space. The appearance of the disease in the latter location is identical to that of cysticercosis involving other CSF-containing spaces. The cysts may “float” in

Antiparasitic drugs

Both praziquantel and albendazole have been extensively and effectively used to treat CNS cysticercosis.3 The courses of the treatments vary between one week to one month. Between 60 and 85% of parasites are killed after such courses (the success rate is higher with albendazole).3 Treatment with antiparasitic medications is considered somewhat controversial because with time all parasites die. In addition, the death of the parasites induced by the drugs results in an inflammatory reaction that

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      The colloidal stage mimics other ring-enhancing lesions. In these cases, DWI may be helpful to differentiate a cysticercosis cyst from a pyogenic abscess because cysticercal cysts are dark.23 Also, ADC values are higher in neurocysticercosis than in TB granulomas.26

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