# Pure neural leprosy in a child: case report and diagnostic challenges

**Authors:** Hortência Aparecida dos Reis Santana, Isabela Pedra Diamantino, Jean Carlos de Araújo Arruda, Pedro Alysson Mota da Silva, Gabrieli Souza dos Santos, Jonatas César Matos de Oliveira, Vanessa Oliveira de Souza, Clécio Ribeiro Costa, Andrea Pereira Macke, Karen Nepomuceno Sá Teles, Fernando do Prado Vieira, Filipe Rocha Lima, Jonilson Berlink Lima

PMC · DOI: 10.1590/0037-8682-0158-2025 · Revista da Sociedade Brasileira de Medicina Tropical · 2026-03-02

## TL;DR

A child with pure neural leprosy, diagnosed via anti-PGL-I test and clinical evaluation, shows the challenges of diagnosing leprosy without skin symptoms.

## Contribution

This case report emphasizes the diagnostic value of anti-PGL-I tests in pure neural leprosy without skin lesions.

## Key findings

- The child showed muscle atrophy and sensory loss with no skin involvement.
- Anti-PGL-I test was positive despite negative slit-skin smear for acid-fast bacilli.
- Multidrug therapy improved sensitivity but not all neurological deficits.

## Abstract

Pure neural leprosy (PNL) is infrequent and manifests exclusively in the peripheral nerves without skin involvement, making the diagnosis more complex. We report the case of a 10-year-old child with muscle atrophy and sensory loss, diagnosed through clinical evaluation, grade 2 disability, and a positive anti-PGL-I test. The slit-skin smear (SSS) was negative for acid-fast bacilli. After 12 months of multidrug therapy, esthesiometric sensitivity improved; however, neurological deficits persisted, requiring anti-inflammatory treatment and physiotherapy. This case highlights the importance of early diagnosis and treatment for preventing disabilities. Tools, such as anti-PGL-I tests and imaging, are crucial, particularly in resource-limited settings.

## Linked entities

- **Diseases:** leprosy (MONDO:0005124)

## Full-text entities

- **Diseases:** sensory loss (MESH:C580162), PNL (MESH:D015441), muscle atrophy (MESH:D009133), inflammatory (MESH:D007249), neurological deficits (MESH:D009461)

## Full text

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## Figures

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## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12990783/full.md

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Source: https://tomesphere.com/paper/PMC12990783