Unusual Toxoplasma infection of the eye and central nervous system in an HIV-positive patient
Authors:
F. Ondriska 1,2; Ľ. Soják 3; V. Boldiš 2; Ľ. Piesecká 4; P. Mikula 5; Ľ. Kováč 2
Authors place of work:
Trnavská univerzita Trnava, Fakulta zdravotníctva a sociálnej práce, Trnava
1; Medirex, a. s., člen Medirex Group, Oddelenie parazitológie, Bratislava
2; Klinika infektológie a geografickej medicíny Lekárskej fakulty Univerzity Komenského, Slovenskej zdravotníckej univerzity a Univerzitnej nemocnice Bratislava
3; Infekčná klinika Fakultnej nemocnice, Nitra
4; Rádiologická klinika Lekárskej fakulty Univerzity Komenského, Slovenskej zdravotníckej univerzity a Univerzitnej nemocnice Bratislava
5
Published in the journal:
Epidemiol. Mikrobiol. Imunol. 71, 2022, č. 3, s. 165-170
Category:
Původní práce
Summary
Objective: To report on a unique combination of cerebral toxoplasmosis and ocular toxoplasmosis in an HIV-positive patient in Slovakia.
Methods: A 35-year-old heterosexual patient who presented with headache and major seizures underwent computed tomography (CT) and magnetic resonance imaging (MRI). Based on clinical findings, serological tests for toxoplasmosis were performed on serum and ocular fluid specimens. PCR was also used to detect Toxoplasma gondii and cytomegalovirus DNA. Goldmann and Witmer coefficient calculation was applied to demonstrate the synthesis of intraocular IgG antibodies.
Results: CT and MRI revealed cystic lesions suspected of metastasis in the occipital and temporal regions, and we searched for the primary tumor. After vision loss in the left eye, which rapidly progressed to complete blindness, an eye examination detected macular edema. Anti-edema treatment was initiated. HIV positivity with a very low CD4 T-cell count (20/μL) was found, and the viral load was 100 400 HIV-RNA copies/ml. The serum was positive for anti-Toxoplasma IgG antibodies (> 200 IU/mL), IgM negative, and IgA borderline. As toxoplasmic encephalitis and retinitis were suspected, antitoxoplasmic therapy with pyrimethamine, spiramycin, and folinic acid was started. The ophthalmologist considered cytomegalovirus retinitis, which was not confirmed by serology or PCR. In contrast, the presence of IgG antibodies in ocular fluid and serum with the calculation of the Goldmann-Witmer coefficient (GW = 32) as well as PCR DNA positivity pointed to Toxoplasma gondii as the etiological agent. Follow-up MRI scan confirmed regression of the pathological lesions, neurological deficit also improved, CD4 T-lymphocytes increased above 200/μL, but blindness of the left eye persisted.
Conclusion: CT and MRI scans offered no clue as to Toxoplasma etiology of the brain and eye involvement in an HIV-positive patient, which was only confirmed by laboratory tests. Due to the delay in the diagnosis of toxoplasmosis, time from the epileptic seizure to treatment initiation was 16 days, which assumedly caused irreversible blindness in the patient.
Keywords:
Toxoplasma gondii – cerebral toxoplasmosis – ocular toxoplasmosis – HIV/AIDS patient
Zdroje
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Štítky
Hygiena a epidemiologie Infekční lékařství MikrobiologieČlánek vyšel v časopise
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