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Extraparenchymal neurocysticercosis in the United States: a case report
© Kelesidis and Tsiodras; licensee BioMed Central Ltd. 2011
Received: 22 February 2011
Accepted: 9 August 2011
Published: 9 August 2011
Neurocysticercosis is endemic in the developing world, but is becoming more common in the United States due to immigration.
A 26-year-old Caucasian man presented with headache, nausea and vomiting and was found to have hydrocephalus and meningitis. Brain imaging and immunological studies were suggestive of neurocysticercosis. Endoscopic removal of the cyst resulted in resolution of symptoms. This case represents a combination of two rare presentations of extraparenchymal neurocysticercosis; intraventricular neurocysticercosis and subarachnoid neurocysticercosis.
Although neurocysticercosis is pleomorphic in its presentation, extraparenchymal neurocysticercosis may be challenging to diagnose and treat. Clinicians should be aware of this condition given increasing incidence in the United States.
Neurocysticercosis (NCC) is the most common disease causing cystic lesions in the central nervous system, especially in developing and tropical countries . However, extraparenchymal NCC may be challenging to diagnose and treat. Increasing immigration from endemic areas will lead to an increasing frequency of extraparenchymal NCC in the United States. Clinicians and neuroradiologists in the United States are often unaware of the radiographic patterns of extraparenchymal NCC and the potentially poor prognosis if not correctly diagnosed and managed. Here, we describe a case of extraparenchymal NCC as a cause of chronic meningitis and hydrochephalus in a patient and we discuss challenges in the diagnosis and management of these cases.
NCC is the most common parasitic infestation of the central nervous system worldwide but is also of emerging importance in the United States, especially in areas with high volumes of immigration from endemic regions of Latin America . A recent study reported an overall frequency of subarachnoid cysts in 2%, ventricular cysts in 6%, and hydrocephalus in 16% of NCC cases . Intraventricular NCC, the presence of Taenia solium cysts in the cerebral ventricular system, occurs in 7-30% of patients with NCC . According to recent studies, extraparenchymal NCC is probably more frequent than previously thought . We have recently reviewed the pathogenesis, diagnosis, clinical manifestations and treatment of extraparenchymal NCC in the United States .
In our case extraparenchymal NCC occurred in an adult male Hispanic immigrant who presented with subacute intracranial hypertension from hydrocephalus and chronic meningitis, characterized by a mild-to-moderate CSF lymphocytic pleocytosis, mild-to-moderate increase in protein, and minimal meningeal signs on exam. Intracranial hypertension is a common manifestation of extraparenchymal NCC and in our case was caused by the direct obstruction of the aqueduct by a cyst and possible blockage of CSF pathways within the subarachnoid space. This blockage may have been due to the inflammatory reaction at the tentorium opening.
Extraparenchymal NCC is associated with a local inflammatory response with high protein concentration and cell counts in the CSF . Clinical manifestations and CSF findings are similar to the more common tuberculous and fungal meningitis [5, 6], since the CSF findings consist of pleocytosis (usually lymphocytic but frequently polymorphonuclear), reduced glucose and elevated protein . In one series of cysticercal meningoencephalitis, confusion with tubercular meningitis was present in 61.5% cases . An important differentiating feature is the presence of eosinophils (above 5%) in the CSF, which is usually seen only in the initial phases of the illness but occurs in only 15% of patients . The presence of chronic meningitis, hydrocephalus, and absence of eosinophils in the CSF of a patient coming from an endemic area for tuberculosis suggested the diagnosis of tuberculous meningitis, and our patient was started on empiric treatment for tuberculosis until a diagnosis of neurocysticercosis was made. It is often common practice to attribute chronic meningitis and hydrocephalus to tubercular meningitis in the presence of appropriate epidemiologic history and treat empirically by shunting and antitubercular therapy. Thus, an astute clinical acumen is required to make the diagnosis of cysticercal meningitis.
Neuroimaging findings of extraparenchymal cysticerci are subtle and are usually not seen by CT. The most common CT finding in subarachnoid NCC is hydrocephalus . In our case, there was hydrocephalus and non-specific cerebral aqueduct stenosis but no obvious imaging evidence of a parasite in the parenchymal or extraparenchymal space. The cyst was located in the aqueduct but was very subtle and was initially missed by the radiologist. Because the cyst membrane is thin and the fluid is isodense with the cerebrospinal fluid, uninflamed extraparenchymal cysticerci are usually not visible on CT scanning and may only reveal subtle, indirect findings on MRI .
MRI has good sensitivity for detecting intraventricular cysticercosis and although it did not initially clear the diagnostic dilemma in this case, contrast MRI was helpful in clarifying the morphology of the lesion. However, only the presence of cystic lesions, demonstrating the scolex of the larval stage of T. solium, can be considered pathognomonic of NCC and an absolute criterion for a definitive diagnosis of the disease [1, 8, 9]. Thus, previous studies have shown that optimal MRI protocols should include axial fluid-attenuated inversion recovery imaging to obtain maximal rates of scolex detection . In our case the exact etiology of the cystic lesion was confirmed on pathological examination of the specimen.
The diagnosis in our case was made based on the presence of a lesion highly suggestive of NCC on neuroimaging study, positive serum immunoassay for the detection of anticysticercal antibodies, positive CSF immunoassay for detection of anticysticercal antibodies and epidemiologic criteria including an individual coming from an area where cysticercosis is endemic . However, extensive and comprehensive revision of the diagnostic criteria of NCC, especially of extraparenchymal NCC, is mandatory according to many recent publications [5, 7, 10].
There is still no consensus regarding optimal treatment strategies in patients with intraventricular NCC [3, 6, 10]. Various therapeutic modalities include antihelminthic medication, microneurosurgical removal, ventriculoperitoneal shunting, and endoscopic management . Medical therapy alone is not favored because of the limited efficacy in such cases, and a risk of developing acute hydrocephalus during the clinical treatment period because of the mobile nature of the intraventricular cyst [3, 11]. Thus, surgical evaluation is necessary prior to medical treatment  and in patients presenting with acute hydrocephalus, surgery is the only option [3, 11]. Endoscopic approaches for intraventricular NCC have been described in recent years and often allow for cyst removal and hydrocephalus treatment, freeing the patient from shunt procedures .
Although subarachnoid cysts were not identified, our patient's clinical presentation and CSF analysis was consistent with cysticercal meningitis and subarachnoid cysticercosis. Thus, our case represents a combination of two rare presentations of extraparenchymal NCC; intraventricular NCC and subarachnoid NCC. There was a consensus among treating neurologists, neurosurgeons and infectious disease consultants to use albendazole at a dose of 15 mg/kg/day for a minimum of 21 days as the antiparasitic treatment. Our patient also received steroids for three weeks and the doses and duration used were equal or bigger than the known standard doses to treat parenchymal disease . However, with controversy in the literature over the optimal management of this condition and without further evidence-based guidelines to help management of extraparenchymal NCC, the decision about the total dose and duration of antiparasitic and steroid therapy was at the discretion of the treating neurologist.
In summary, the case presented here is an important reminder that intraventricular NCC should be considered in the differential diagnosis of obstructive hydrocephalus with the radiographic appearance of a cystic lesion in the third, aqueduct, or fourth ventricle. Extraparenchymal NCC may be a more common form of NCC in the United States than previously thought. Because clinicians in the US outside the southwest US are often unfamiliar with NCC as a cause of chronic meningitis, chronic ventriculitis, or hydrocephalus without obvious cysts, the diagnosis of extraparenchymal NCC often depends on the correct interpretation of neuroimaging which may miss the diagnosis. Thus, meningeal and intraventricular NCC should always be considered by clinicians and radiologists in the differential diagnosis of chronic meningitis and hydrocephalus, particularly in patients from Latin America.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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