Surgical management outcome of cerebral schistosomiasis: a case report and review of the literature

Schistosomiasis is estimated to affect more than 200 million people worldwide, who are infected by contact with contaminated water [1]. Central nervous system manifestations are a result of the inflammatory response to egg deposition; recent infection is usually not present [2]. The commonest cause of cerebral schistosomiasis is Schistosoma japonicum [3], but there are many cases due to Schistosoma mansoni reported in the literature [4]. We report a rare case of active cerebral schistosomiasis in a young male patient presenting with headache and convulsions, where a lesion occupying the left parieto-occipital space was revealed on magnetic resonance imaging (MRI). The pathology, clinical presentation, diagnostic evaluation, and methods of pre- and postoperative treatment of cerebral schistosomiasis are reviewed.

A 24-year-old, previously healthy Afro-asiatic man presented to our neurosurgical outpatient clinic complaining of headache for 3 months, which was followed by one attack of generalized tonic–clonic convulsions, which prompted him to seek medical advice. He reported no other associated signs or symptoms. Upon general examination, the patient looked unwell, but no pallor, jaundice, or cyanosis was observed. His vital signs were all within the normal range. On neurological examination, he was conscious, oriented to time, place, and person, with a Glasgow Coma Scale score of 15 out of 15 and normal papillary reaction and size bilaterally. The patient had power grade 4+ in both the upper and lower right limbs, with normal tone and reflexes in all joints. Systemic review was unremarkable. Laboratory investigations including stool and urine general test results were unremarkable, so no further cerebral spinal fluid analysis was pursued. Initial plain head computed tomography (CT) showed a focal area of high density within the left parietal region. An MRI of the brain was then performed and showed a fairly well-defined 1.8 × 1 cm lobulated, cortical-based intra-axial lesion within the left posterior parietal region. The lesion demonstrated homogeneous enhancement and had associated moderate perilesional vasogenic edema with only a mild localized mass effect. No other focal lesions were seen (Fig. 1). A list of possible differential diagnoses was made and included granulomatous lesion, lymphoma, a primary glial neoplasm, and less likely meningioma.

Magnetic resonance spectroscopy, although nonspecific, demonstrated a choline peak suggestive of cell membrane turnover that can be seen in a number of different conditions including neoplasms, demyelination, inflammation, and gliosis. Correlating this with the patient age and history, an inflammatory lesion was thought to be more likely (Fig. 2). The patient was then admitted and underwent craniotomy and total microsurgical resection of the lesion. Histopathology results showed viable and calcified Schistosoma mansoni ova with marked mixed inflammatory infiltrate composed of granulomas and eosinophils, all features consistent with active cerebral schistosomiasis (Fig. 3). Oral administration of antiparasitic praziquantel was initiated at a dose of 20 mg/kg twice a day for a total of 3 days along with orally administered corticosteroids for 2 weeks. The patient was discharged in good condition with improving neurological condition. A postoperative follow-up MRI was performed 3 months later and showed complete resection of the lesion (Fig. 4). Marked neurological improvement was noted at 1-month, 3-month, and 6-month follow-up visits. The patient regained full power and had no further convulsions.

It is estimated that more than 200 million people worldwide are infected with schistosomiasis after contact with contaminants [1]. Five species are known to infect humans, with Schistosoma japonicum the most common species affecting the human nervous system [3]. Contact with water that carries the larva of the parasite may result in schistosomiasis [5]. After direct contact, the larva enters the human blood through the skin. Days later, worms migrate to the inferior mesenteric vessels, and the production of eggs begins within 6 weeks following infection [5]. This process continues for the whole life of the worm, or about 3–5 years [6]. The eggs pass through the blood vessel lumen and the intestinal mucosa; they terminate in fecal materials, and the life cycle ends when the eggs release miracidia [5]. The cerebral form of schistosomiasis is thought to result from migration of the worms through the vertebral venous plexus (Batson plexus); in this valveless system, worms are able to migrate and produce eggs directly in the brain [6].

Schistosomiasis of the central nervous system occurs very rarely, with Schistosoma japonicum commonly causing cerebral lesions, and Schistosoma mansoni and Schistosoma haematobium commonly causing spinal cord lesions. Schistosoma mansoni and Schistosoma haematobium are unusual causes of cerebral mass lesions [7]. Pittella et al. reported four patients with cerebral Schistosoma mansoni infection and reviewed a few cases that were reported then in the literature [8].

Central nervous system manifestations are a result of the inflammatory response to egg deposition in the brain and spinal cord, and are usually seen in patients with recent infection with no evidence of systemic illness [2]. Supra- or infratentorial foci may result in headache, seizure, and other signs of raised intracranial pressure. Cerebral schistosomiasis is more common in Schistosoma japonicum, but an increasing number of cases due to Schistosoma mansoni have been reported in the literature [4, 6].

Schistosomiasis of the spinal cord is a rare condition but is well reported in the literature, especially in sub-Saharan African countries, where several case reports and series have been published. Spinal cord schistosomiasis may present clinically by myelopathy, radiculopathy, or both [9].

In Sudan, a case series was reported in which 5 of 200 patients with spinal cord compression were found to have schistosomiasis and underwent surgery and medical treatment, with excellent outcome; diagnosis of those who underwent surgery was confirmed only after histopathological examination [10]. Another case series of 27 patients was reported by El Malik et al., where all patients underwent regular blood tests, serological investigations, and radiological examination, among which two underwent surgical intervention due to expansion of the lesion with no response to medical management [11].

Operative cases of cerebral schistosomiasis are very unusual and have been reported in the literature on rare occasions. Schistosoma japonicum eggs in the brain were first described by Tsunoda and Shimamura in 1906 [12]. In 1936, Egan et al. reported two neurological cases of Schistosoma japonicum among 12 English sailors who went swimming in the Yangtze River [13].

Patients have been incorrectly diagnosed as having brain tumors, specifically gliomas, due to radiological findings consistent with glioma on CT and MRI [2]. Heterogeneous enhancement was seen mainly at the cerebellum and occasionally at the thalamus, parietal, occipital, and frontal regions [6, 8].

Sanelli et al. reported what they called an arborized enhancement pattern with central linear enhancement, which may be significant for cerebral schistosomiasis [14]. Huang et al. concluded that diffusion-weighted MRI with apparent diffusion coefficient values may be a useful tool in the diagnosis of cerebral schistosomiasis [15]. A combination of laboratory and radiological investigations are required in order to reach diagnosis in certain cases [2].

Diagnosis of cerebral Schistosoma infection is a challenging task. Kato-Katz thick-smear stool examination, which is the most practical laboratory examination for the investigation, can determine the presence of eggs in feces [16]. Imai et al. reported the first case of cerebral schistosomiasis due to Schistosoma haematobium, which was diagnosed by molecular methods; polymerase chain reaction assay is a promising method for definitive diagnosis and species identification in cases of cerebral schistosomiasis when Schistosoma ova in urine or stool specimens can be identified [17]. Histopathological examination remains in the only method for reaching a definite diagnosis [1].

The therapeutic strategy in patients with new-onset seizures should be based on the type of seizures and on the epilepsy syndrome. Long-term antiepileptic drug treatment is typically not indicated [6]. The treatment of cerebral schistosomiasis is highly effective and safe; total or partial resection of the lesion is needed to confirm diagnosis and to relieve the signs and symptoms [2]. Medical treatment after diagnosis with oxamniquine and praziquantel, which are the most effective antiparasitic drugs for treating schistosomiasis, is essential [6] to kill the adult worms, and corticosteroids reduce granulomatous inflammation and are used for all Schistosoma subtypes [18].

Surgical management of cerebral schistosomiasis is safe and highly effective in cases where the diagnostic laboratory and radiological findings are inconclusive, leading to difficulty in initiating appropriate medical management. Surgically, total resection of the lesion is the best choice for confirming diagnosis and alleviating symptoms. Medical treatment should be started after surgery and confirmed diagnosis; oxamniquine and praziquantel are effective antiparasitic drugs. These drugs, used alongside corticosteroids, kill the adult worms and reduce the granulomatous inflammation, respectively.