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NEUROLOGY 1993;43:2035
© 1993 American Academy of Neurology

Choroid plexus infection in cerebral toxoplasmosis in AIDS patients

M. F. Falangola, MD and C. K. Petito, MD

From the Department of Pathology, The New York Hospital-Cornell University Medical College, New York, NY.

We evaluated the postmortem incidence of choroid plexus infection in cerebral toxoplasmosis in 17 patients with acquired immune deficiency syndrome (AIDS) and cerebral toxoplasmosis and, by immunohistochemistry, identified Toxoplasma gondii tachyzoites in this structure in 53% of all cases. They were present in 78% of the nine cases with the acute necrotizing stages of CNS toxoplasmosis but were less frequent (20%) in patients with only the healed cystic lesions of toxoplasmosis. Large necrotizing abscesses of the choroid plexus were found in three of the patients. In one of these, the choroid plexus was the sole site of CNS infection, which presented as radiographically documented masses in the third and fourth ventricles associated with obstructive hydrocephalus. These results demonstrate that infection of the choroid plexus is common with cerebral toxoplasmosis and suggest that this infection should be included in the differential diagnosis of intra- or periventricular lesions in patients with AIDS. In addition, the high frequency of choroid plexus infection with acute cerebral toxoplasmosis suggests that cerebral toxoplasmosis in the immunosuppressed patient may be due to hematogenous spread to the choroid plexus from reactivation of latent organisms from systemic organs rather than to reactivation of latent organisms within the brain itself. Furthermore, the high frequency of choroid plexitis offers the potential for CSF dissemination of this infection.

Address correspondence and reprint requests to C.K. Petito, MD, University of Miami School of Medicine, Department of Pathology (R-5), Papanicolaou Research Building, Room 417, 1550 N.W. 10th Avenue, Miami, FL 33136.

Supported by grants from the Conselho Nacional de Desenvolvimento Cientifico e Technologico (M.F.F.) and the National Institutes of Health RO1 NS27416 (C.K.P.).

Received December 14, 1992. Accepted for publication in final form February 17, 1993.







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