BACKGROUND: In Guadeloupe, cases of neurocysticercosis have been rarel
y observed in people recently immigrated from Haiti. We followed 2 wom
en with seizures, associated with meningitis or encephalitis. CASE REP
ORT: Computed tomography scan and muscle Xray have displayed specific
features of cysticercosis with small diffuse calcifications. This was
associated with positive antibodies for cysticercosis. After respectiv
ely 5 and 17 years, these patients developed recurrent manifestations
of neurocysticercosis with subacute, guile silent meningitis after pre
gnancy, with CSF increased cells count (180 lymphocytes/mm(3)), raised
protein level (0.6g/l) and positive antibodies for cysticercosis in t
he first case, and corticai granuloma with fever and repetitive seizur
es in the second. DISCUSSION: These observations suggest that the pati
ents were chronically infested, for more than 5 years. Although the br
ain lesions were quiescent for many years, new lesions responsible for
inflammatory cysts occurred while they still lived outside her native
endemic area. In such cases, treatment would benefit to the patient b
y breaking down the auto-infestation cycle.