# When Appearances Deceive: A Case Report of Neurocysticercosis Masquerading As Tuberculoma

**Authors:** Hrithik Dakssesh Putta Nagarajan, Keerthivasan Selvanathan, Tejashvi Rameshkumar, Nitish Thirugnanasambandam, Md Ramij Biswas

PMC · DOI: 10.7759/cureus.103762 · Cureus · 2026-02-17

## TL;DR

A 17-year-old patient was misdiagnosed with a brain tuberculosis for eight years when she actually had neurocysticercosis, highlighting the need for careful diagnosis.

## Contribution

This case report highlights diagnostic challenges in distinguishing neurocysticercosis from tuberculoma using imaging in resource-limited settings.

## Key findings

- The patient was misdiagnosed with cerebral tuberculoma for eight years based on imaging alone.
- Negative tuberculosis tests and treatment response confirmed the correct diagnosis of neurocysticercosis.
- The case emphasizes the importance of combining clinical and radiological data to avoid misdiagnosis.

## Abstract

Neurocysticercosis (NCC) is a predominant cause of acquired epilepsy globally and often resembles cerebral tuberculoma in neuroimaging, particularly in regions where tuberculosis is prevalent. Diagnostic challenges are exacerbated in resource-limited settings due to financial limitations, restricted access to advanced diagnostic tools, and insufficient longitudinal medical records. We report a case of a 17-year-old immunocompetent female with recurrent generalized seizures who was repeatedly misdiagnosed with cerebral tuberculoma over an eight-year period and treated with multiple courses of anti-tubercular therapy based solely on imaging findings. During the current evaluation, magnetic resonance imaging identified a solitary, small, non-enhancing T2 hypointense lesion with surrounding edema in the right frontal lobe, prompting a differential diagnosis of NCC versus tuberculoma. Negative QuantiFERON-TB Gold (QFT-G, Cellestis Limited, Carnegie, Victoria, Australia) testing, normal chest radiography, absence of systemic tuberculosis, and prior extensive exposure to anti-tubercular therapy favored NCC. Treatment with albendazole and corticosteroids resulted in complete seizure control without recurrence. This case underscores the necessity for meticulous clinic-radiological correlation and increased diagnostic vigilance to prevent misdiagnosis and unnecessary treatment, particularly in resource-constrained environments.

## Linked entities

- **Chemicals:** albendazole (PubChem CID 2082)
- **Diseases:** epilepsy (MONDO:0005027), tuberculosis (MONDO:0018076)

## Full-text entities

- **Diseases:** Tuberculoma (MESH:D014375), epilepsy (MESH:D004827), NCC (MESH:D020019), systemic tuberculosis (MESH:D014376), edema (MESH:D004487), seizure (MESH:D012640)
- **Chemicals:** albendazole (MESH:D015766), QFT (-)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13001127/full.md

## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC13001127/full.md

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Source: https://tomesphere.com/paper/PMC13001127