Abstract.A 37-year-old woman with a known history of longstanding neurocysticercosis presented with a threeday history of new onset headache. Several years prior to her current presentation, she had undergone cysticidal treatment and was assumed to be cured of active disease. Computed tomography and magnetic resonance imaging studies done three months prior to presentation showed multiple intracerebral calcified lesions consistent with resolved neurocysticercosis. Physical and laboratory findings were noncontributory. Imaging studies showed the same previously calcified lesions, but they were now surrounded by large amounts of edema. This case represents a unique report of reactivation of neurocysticercosis and raises interesting questions about the natural history of this infection.Neurocysticercosis is caused by the larval stage of the tapeworm Taenia solium that inhabits the small bowel of an infected human host. Initial clinical manifestations of central nervous infection include seizures, focal neurologic deficits, and mental status changes. 1 With cysticidal treatment, the natural history of the infection is accelerated. 2 A successfully treated lesion rapidly progresses from an inert cyst with a live scolex to involution and calcification. During the process of cyst death the host mounts an inflammatory response to released larval proteins, accompanied by a cellular infiltrate and edema. Although seizures may persist after treatment, patients with calcified lesions are assumed to be cured of active disease. 2 We report a case of neurocysticercosis in which a patient who was assumed to be cured of active infection presented with sudden onset of headache, associated with inflammation and edema around lesions previously shown to be calcified.
CASE REPORTA 37-year-old woman, originally from Ecuador and with a known history of neurocysticercosis, presented to the emergency department of The Toronto Hospital on January 7, 1997. The patient was well until early December 1996, when she developed a self-limited flu-like illness consisting of malaise, fever, and sore throat. Two weeks later, fever recurred along with erythema nodosum (her third recurrence since 1989) for which she was admitted to hospital for five days and treated with solumedrol and amoxicillin. One week after discharge from the hospital her headaches began. The headaches were frontal in location and occurred intermittently, associated with vomiting, slowed mentation, and episodic visual scintillations.Her medical history revealed that in 1987 she had been diagnosed with neurocysticercosis when she presented with severe headaches and grand mal seizures. Her computed tomography (CT) scan had shown numerous active cystic lesions and hydrocephalus. The patient underwent ventriculoperitoneal (VP) shunt placement in 1988 and cysticidal treatment with albendazole in 1991. Subsequently, she remained relatively asymptomatic, receiving phenobarbitol for seizure control. Over several years, on repeat imaging studies, numerous parenchymal lesions were noted ...