Neurocysticercosis In Detroit, Michigan
J Burneo, G Barkley
Citation
J Burneo, G Barkley. Neurocysticercosis In Detroit, Michigan. The Internet Journal of Neurology. 2002 Volume 2 Number 1.
Abstract
Neurocysticercosis (NC) is the most frequent parasitic disease of the Central Nervous System, and the most frequent cause of epilepsy worldwide (1,2,3). It is endemic in many regions of the world, and certain parts of the United States particularly the southwestern states of California and New Mexico. NC represents a major cause of morbidity among the immigrant Hispanic population. However, as the number of immigrants expanded, especially those from endemic areas, there have also been a progressive increase in the cases of NC in other parts of the country, in the past ten years.
We report nine cases of patients with NC, diagnosed at Henry Ford Hospital, in Detroit, between 1989 and 1999, were identified. All of them were immigrants to the United States, eight from Mexico and one from India.
Introduction
Neurocysticercosis (NC) is the most frequent parasitic disease of the Central Nervous System, and the most frequent cause of epilepsy worldwide (1,2,3). It is endemic in many regions of the world, and certain parts of the United States particularly the southwestern states of California and New Mexico. NC represents a major cause of morbidity among the immigrant Hispanic population. However, as the number of immigrants expanded, especially those from endemic areas, there have also been a progressive increase in the cases of NC in other parts of the country, in the past ten years.
Michigan is not considered an endemic region for NC. However, the latest U. S. census data has shown that the Hispanic population in Michigan has nearly doubled in the past decade, rising from 2.2% in 1990 to 3.5% in 2000 (4). Most of the increased Hispanic immigration into Michigan has come from people from Mexico. It is expected that a proportionate increase in NC will be seen in local hospitals. To estimate the magnitude of this problem, we reviewed the medical records at Henry Ford Hospital in Detroit, Michigan, for patients with NC in the past decade.
Cases
Nine patients with NC, diagnosed at Henry Ford Hospital, in Detroit, between 1989 and 1999, were identified (Table). All of them were immigrants to the United States, eight from Mexico and one from India.
None of the patients acquired the disease in Detroit or the United States. Seizures were the most common initial manifestation. CT and/or MRI provided the diagnosis of NC and contributed to follow-up. Brain imaging showed both viable cysts and calcifications (Figures). Cysticercosis serology, with ELISA, was performed in 3 out of 9 patients and was positive in only one patient and negative in two of them. Antiparasite treatment with albendazole or praziquantel was provided to four patients, and surgical intervention to one. There were no deaths.
Discussion
The clinical manifestations in the patients in our series do not differ from the ones reported in the medical literature. NC is a pleomorphic disease, although sometimes may not produce any clinical manifestation (2,3). Patients may seek medical attention because of headaches, seizures, and focal neurological or neurobehavioral manifestations.
NC is the leading cause of adult-onset epilepsy in areas of the world where the disease is endemic, particularly in the developing countries of Latin America, Asia, and Africa. Large series of patients with adult-onset epilepsy have demonstrated that NC occurs in up to 50% of cases, usually representing the single most common cause of this syndrome (5,6,7,8).
In the United States,
Because the fast growth of the immigrant population in Michigan which increased by 60.7% in the past 10 years, neurological manifestations, especially seizures, in patients coming from endemic areas should prompt a search for NC with brain imaging. Serology should be part of the diagnosis work-up but was only performed in one third of the patients in our series. Antiparasitic medication should be started when appropriate. Resolution of symptoms and radiological findings with treatment confirms the diagnosis in cases in which the diagnosis may not be certain initially.
Neurologists and primary care physicians should be aware that NC is currently no longer a tropical disease seen only in the southwestern United States. NC should be considered in the differential diagnosis of immigrant patients with neurologic manifestations such as seizures in the northern states as well.
Correspondence to
Jorge G Burneo, MD UAB-Epilepsy Center Department of Neurology University of Alabama at Birmingham. CIRC 312. 1719 6th Avenue S. Birmingham, AL. 35294-0021 E-mail: jburneo@uab.edu Fax: (205) 934-3866 Phone: (205) 975-6255