RESUMO
This study reflects our experience in managing Sudanese children with different cranial conditions through external ventricular drainage (EVD): indications for EVD, pathologies faced, and early outcome. A prospective review of cases operated at the National Center for Neurological Sciences was carried out during the period from February 2014 to February 2016. The patients were closely followed up till EVD removal and discharge. Thirty-five Sudanese children were included in the study (age range between 6 days and 7 years). Majority of the cases had posterior fossa tumor with obstructive hydrocephalus (n = 19, 54.3%). Twenty (57.1%) patients presented with a decreased level of consciousness, while 28 (80%) patients presented with symptoms and signs of raised intracranial pressure (ICP). The decision for EVD was made preoperatively based on positive cranial computed tomography/magnetic resonance imaging findings in 10 (28.6%) patients. Additionally, 28 (80%) patients responded to single injectable antibiotic therapy with an average duration of 22 days. Subsequently, 25 (71.4%) patients improved or got cured, 5 deteriorated, and 11 died. We conclude that EVD can be used for many indications, including obstructive, postinfectious, and postmeningitic hydrocephalus as well as intraventricular hemorrhage. Most patients may present with either deteriorating levels of consciousness or symptoms and signs of raised ICP, but few of them may have positive brain imaging findings and therefore the decision for EVD was made intraoperatively. The average duration for EVD use was 3 weeks with single antibiotic therapy use, which was found as effective as when combined with intraventricular therapy.
RESUMO
BACKGROUND: Schistosomiasis is a parasitic infection that commonly affects the gastrointestinal and genitourinary tracts. Cerebral schistosomiasis is rare, and few operative cases have been reported in the literature. Diagnosis is usually challenging due to the similarity of the lesion to many other brain conditions. Treatment usually requires surgical resection combined with the use of antiparasitic agents, which often results in good outcomes and excellent prognosis. CASE PRESENTATION: A 24-year-old, previously healthy Afro-asiatic man presented to our neurosurgical outpatient clinic complaining of headache and an attack of convulsions. On examination, he had bilateral lower limb weakness more on the right side. Laboratory investigations including stool and urine general test results were unremarkable. Magnetic resonance imaging of the brain was performed and showed an intra-axial left parietal mass; a granulomatous lesion was suggested in the differential diagnoses. The patient underwent craniotomy and total resection of the lesion. Histopathology confirmed the presence of active cerebral Schistosoma mansoni infection. Orally administered praziquantel was initiated at a dose of 20 mg/kg twice a day for a total of 3 days along with oral administration of corticosteroids for 2 weeks. The patient improved postoperatively without residual weakness and with no further convulsions. CONCLUSION: Cerebral schistosomiasis is a rare but important consideration in the list of differential diagnoses of cerebral space-occupying lesions. This is of particular importance in in endemic areas like Sudan. In order to reach a diagnosis, careful social and occupational history need to be obtained and correlated with the clinical, laboratory, and radiological findings. Surgical resection along with the use of proper antiparasitic agents usually provides the best clinical outcomes.
