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Published on: August 31, 2013
Lyme Disease and Papilledema: A Retrospective Study on Clinical Characteristics and Outcomes
Joseph Vithayathil1,2, Akash Virupakshaiah3, Geraldine Liu1
1Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Insights
Children with Lyme disease and papilledema often recover fully with antibiotic treatment, even with cerebrospinal fluid pleocytosis. Most cases show resolution without lasting deficits.
Area of Science:
- Pediatric Neurology
- Infectious Diseases
- Ophthalmology
Background:
- Papilledema, or swelling of the optic disc, can be a serious complication in pediatric patients.
- Lyme disease, a tick-borne illness, can present with various neurological manifestations.
Purpose of the Study:
- To describe the clinical features, treatments, and outcomes of pediatric patients diagnosed with both papilledema and Lyme disease.
- To analyze the relationship between cerebrospinal fluid findings and treatment response.
Main Methods:
- A retrospective cohort study was conducted involving children aged 1-18 years diagnosed with papilledema and Lyme disease between 1995 and 2019.
- Data were collected through medical record abstraction and family surveys.
Main Results:
- Of 44 children, 66% had cranial neuropathies and 78% had cerebrospinal fluid (CSF) pleocytosis. All received antibiotics, and 61% also received acetazolamide.
- Eighty-six percent of children with follow-up data experienced full symptom resolution.
- Recovery rates did not significantly differ based on antibiotic route or CSF pleocytosis.
Conclusions:
- Papilledema in pediatric Lyme disease can occur with or without CSF pleocytosis.
- The majority of children achieve full recovery without residual deficits following appropriate treatment.
- Exceptions to full recovery exist, highlighting the need for continued monitoring.
Objective:
Describe the clinical characteristics, treatment strategies, and outcome data of children with papilledema associated with Lyme disease at a large tertiary care pediatric hospital.
Methods:
Retrospective cohort study of children 1-18 years old who received care at our institution between 1995 and 2019 with concurrent diagnoses of papilledema and Lyme disease. Data were abstracted from records and prospective family surveys.
Results:
Among 44 children included (median age 9.7 years), 66% (29/44) had additional cranial neuropathies, and 78% (32/41) had cerebrospinal fluid pleocytosis. All children were treated with antibiotics (39% oral, 55% intravenous, 7% both); 61% (27/44) were also treated with oral acetazolamide. Symptoms fully resolved in 86% (30/35) of children with follow-up data. Proportion recovered did not significantly differ by antibiotic administration route or presence/absence of cerebrospinal fluid pleocytosis.
Conclusions:
Papilledema in Lyme disease may occur with or without cerebrospinal fluid pleocytosis. Most children recover without residual deficits following treatment, although exceptions exist.
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