TY - JOUR
T1 - Neuroschistosomiasis
AU - Ross, Allen G.
AU - McManus, Donald P.
AU - Farrar, Jeremy
AU - Hunstman, Richard J.
AU - Gray, Darren J.
AU - Li, Yue Sheng
N1 - Funding Information:
This study was supported by the United Nations Development Programme/World Bank/World Health Organization Special Program for Research and Training in Tropical Diseases (Dr. Li and Prof. McManus), the National Health and Medical Research Council of Australia (Dr. Li and Prof. McManus), the Wellcome Trust (UK) (Dr. Li and Prof. McManus), the Sandler Foundation (USA) (Prof. McManus), the Dana Foundation (USA) (Dr. Li and Prof. McManus) and the National Institute of Allergy and Infectious Diseases (Dr. Li and Prof. McManus). Dr. Li Yuesheng is a Howard Hughes Medical Institute Scholar, USA.
PY - 2012/1
Y1 - 2012/1
N2 - Schistosomiasis (bilharzia) is a neglected tropical disease caused by digenetic trematode platyhelminths of the genus Schistosoma. Neuroschistosomiasis is one of the most severe clinical outcomes associated with schistosome infection. Neurological complications early during the course of infection are thought to occur through in situ egg deposition following aberrant migration of adult worms to the brain or spinal cord. The presence of eggs in the CNS induces a cell-mediated Th2-driven periovular granulomatous reaction. The mass effect of thousands of eggs and the large granulomas concentrated within the brain or spinal cord explain the signs and symptoms of increased intracranial pressure, myelopathy, radiculopathy and subsequent clinical sequelae. Myelopathy (acute transverse myelitis and subacute myeloradiculopathy) of the lumbosacral region is the most common neurological manifestation of S. mansoni or S. haematobium infection, whereas acute encephalitis of the cortex, subcortical white matter, basal ganglia or internal capsule is typical of S. japonicum infection. Cerebral complications include encephalopathy with headache, visual impairment, delirium, seizures, motor deficits and ataxia, whereas spinal symptoms include lumbar pain, lower limb radicular pain, muscle weakness, sensory loss and bladder dysfunction. The finding of eggs in the stool or a positive serology, provides supportive but not direct evidence of neuroschistosomiasis. A definitive diagnosis can only be made with histopathological study showing Schistosoma eggs and granulomas. Schistosomicidal drugs (notably praziquantel), steroids and surgery are currently used for the treatment of neuroschistosomiasis. During the 'acute phase' of the disease, neuroschistosomiasis is treated with corticosteroids which are augmented with a course of praziquantel once female worm ovipositioning commences. Surgery should be reserved for special cases such as in those with evidence of medullary compression and in those who deteriorate despite clinical management.
AB - Schistosomiasis (bilharzia) is a neglected tropical disease caused by digenetic trematode platyhelminths of the genus Schistosoma. Neuroschistosomiasis is one of the most severe clinical outcomes associated with schistosome infection. Neurological complications early during the course of infection are thought to occur through in situ egg deposition following aberrant migration of adult worms to the brain or spinal cord. The presence of eggs in the CNS induces a cell-mediated Th2-driven periovular granulomatous reaction. The mass effect of thousands of eggs and the large granulomas concentrated within the brain or spinal cord explain the signs and symptoms of increased intracranial pressure, myelopathy, radiculopathy and subsequent clinical sequelae. Myelopathy (acute transverse myelitis and subacute myeloradiculopathy) of the lumbosacral region is the most common neurological manifestation of S. mansoni or S. haematobium infection, whereas acute encephalitis of the cortex, subcortical white matter, basal ganglia or internal capsule is typical of S. japonicum infection. Cerebral complications include encephalopathy with headache, visual impairment, delirium, seizures, motor deficits and ataxia, whereas spinal symptoms include lumbar pain, lower limb radicular pain, muscle weakness, sensory loss and bladder dysfunction. The finding of eggs in the stool or a positive serology, provides supportive but not direct evidence of neuroschistosomiasis. A definitive diagnosis can only be made with histopathological study showing Schistosoma eggs and granulomas. Schistosomicidal drugs (notably praziquantel), steroids and surgery are currently used for the treatment of neuroschistosomiasis. During the 'acute phase' of the disease, neuroschistosomiasis is treated with corticosteroids which are augmented with a course of praziquantel once female worm ovipositioning commences. Surgery should be reserved for special cases such as in those with evidence of medullary compression and in those who deteriorate despite clinical management.
KW - Bilharzia
KW - Neuroschistosomiasis
KW - Praziquantel
KW - Schistosomiasis
UR - http://www.scopus.com/inward/record.url?scp=84856693964&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84856693964&partnerID=8YFLogxK
U2 - 10.1007/s00415-011-6133-7
DO - 10.1007/s00415-011-6133-7
M3 - Review article
C2 - 21674195
AN - SCOPUS:84856693964
SN - 0340-5354
VL - 259
SP - 22
EP - 32
JO - Journal of Neurology
JF - Journal of Neurology
IS - 1
ER -