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Published on: December 9, 2014
[Atypical presentation of infant toxocariasis: About a case]
Iris Sayas1, Pamela Álvarez1, Rossana Pajuelo1
1Hospital Nacional Dos de Mayo, Lima, Perú.
Insights
This case study highlights an unusual presentation of toxocariasis in a child from the Peruvian Amazon. Prompt diagnosis and albendazole treatment led to a favorable outcome for the young patient.
Area of Science:
- Parasitology
- Pediatric Infectious Diseases
- Clinical Case Reports
Background:
- Toxocariasis, a parasitic infection, typically presents with visceral, ocular, or covert symptoms.
- Atypical presentations can pose diagnostic challenges, especially in endemic regions like the Peruvian Amazon.
Observation:
- An 8-year-old girl presented with abdominal pain, pallor, geophagia, an abdominal mass, and generalized lymphadenopathy.
- No respiratory, dermal, ocular, or neurological symptoms were reported.
- Significant peripheral eosinophilia and moderate eosinophilia in cerebrospinal fluid were noted.
Findings:
- Enzyme-linked immunosorbent assay (ELISA) confirmed toxocariasis by detecting IgG and IgM anti-Toxocara antibodies.
- The atypical clinical presentation included abdominal symptoms and lymphadenopathy without typical toxocariasis manifestations.
Implications:
- This case underscores the importance of considering toxocariasis in pediatric patients with unexplained abdominal symptoms and eosinophilia, even with atypical disease patterns.
- Early diagnosis through serology and prompt treatment with albendazole are crucial for favorable outcomes in toxocariasis.
- Highlights the need for increased awareness of parasitic infections in resource-limited settings with potential for zoonotic transmission.
Abstract:
We present the case of an 8-year-old girl with an atypical presentation of toxocariasis, from the Peruvian Amazon. A month ago, the clinical presentation was characterized by the presence of abdominal pain, paleness and geophagia, associated with an abdominal mass and generalized lymphadenopathy. There were no respiratory, dermal, ocular or neurological symptoms. Marked peripheral eosinophilia was found in the blood count, and moderate eosinophilia in the spinal cord aspírate. The diagnosis was confirmed by serology with the enzyme-linked immunosorbent assay (ELISA), which showed the presence of IgG and IgM anti- Toxocara antibodies. Treatment with albendazole 400 mg once daily was administered for five days with favorable evolution.
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