# A case report of arsenic-induced peripheral neuropathy misdiagnosed as Guillain-Barré syndrome

**Authors:** Shanshan Fu, Guanao Wu, Yibo Zhan, Hui Xia, Chang Zhou, Jingjing Zeng, Ye Tang, Boyan Pan, Zequan Zheng, Min Zhao, Yuanqi Zhao, Haoyou Xu

PMC · DOI: 10.3389/ftox.2026.1722489 · Frontiers in Toxicology · 2026-02-05

## TL;DR

A man's arsenic poisoning was initially mistaken for Guillain-Barré syndrome, highlighting the importance of considering heavy metal toxicity in similar cases.

## Contribution

This case report highlights the diagnostic challenges of distinguishing arsenic-induced neuropathy from Guillain-Barré syndrome.

## Key findings

- Arsenic-induced peripheral neuropathy can mimic Guillain-Barré syndrome clinically.
- Diagnostic confirmation relied on elevated arsenic levels in hair and nail samples.
- Early recognition of arsenic toxicity through history and physical findings improved prognosis.

## Abstract

To explore the clinical characteristics and misdiagnosis causes of arsenic-induced peripheral neuropathy.

We report a case of arsenic-induced peripheral neuropathy initially misdiagnosed as Guillain-Barré syndrome, with analysis of clinical characteristics, diagnostic workup and therapeutic management, supplemented by literature review.

A 58-year-old male presented with progressive peripheral neuropathy, initially diagnosed with Guillain-Barré syndrome but later suspected as chronic inflammatory demyelinating polyneuropathy. However, his symptoms progressed despite standard immunotherapy, developing generalized motor deficits, myokymia, ascending sensory loss, and facial palsy. Careful reevaluation revealed critical diagnostic clues: a history of intermittent topical application of an unidentified herbal medicine preceding symptom onset, accompanying gastrointestinal prodromal symptoms, and characteristic physical findings including Mee’s lines, lower limb hyperpigmentation, and foot hyperkeratosis. Subsequent laboratory testing confirmed markedly elevated arsenic levels in nail and hair samples, ultimately establishing the diagnosis of arsenic-induced peripheral neuropathy.

Arsenic-induced peripheral neuropathy can clinically mimic Guillain-Barré syndrome. For immunotherapy-refractory cases, clinicians should maintain high suspicion for potential heavy metal poisoning. Careful elicitation of toxic exposure history and recognition of characteristic dermatologic findings are critical for definitive diagnosis, as early recognition significantly improves prognosis.

## Linked entities

- **Chemicals:** arsenic (PubChem CID 5359596)
- **Diseases:** peripheral neuropathy (MONDO:0003620), Guillain-Barré syndrome (MONDO:0016218), chronic inflammatory demyelinating polyneuropathy (MONDO:0006702)

## Full-text entities

- **Genes:** NGF (nerve growth factor) [NCBI Gene 4803] {aka Beta-NGF, HSAN5, NGFB}, PCAT2 (prostate cancer associated transcript 2) [NCBI Gene 103164619] {aka CARLO4, CARLo-4, PCA2, TCONS_00015167}, GRDX (Graves disease, susceptibility to, X-linked) [NCBI Gene 117189] {aka GD3}
- **Diseases:** hemorrhoid (MESH:D006484), motor deficits (MESH:D009461), vomiting (MESH:D014839), bilateral toe and heel hyperkeratosis (MESH:D000070592), paraneoplastic (MESH:D010257), nausea (MESH:D009325), sensory neuropathy (MESH:D009477), immune-mediated disorders (MESH:C567355), diarrhea (MESH:D003967), GBS (MESH:D020275), tumor (MESH:D009369), sensory disturbances (MESH:D012678), muscle weakness (MESH:D018908), poisoning (MESH:D011041), polyradiculoneuropathy (MESH:D011129), anorexia (MESH:D000855), Hyperkeratosis (MESH:D017488), pigmentation (MESH:D010859), Liver fibrosis (MESH:D008103), Neurotrophic medications (MESH:D009133), gastrointestinal symptoms (MESH:D012817), inflammatory (MESH:D007249), CIDP (MESH:D020277), Hyperpigmentation (MESH:D017495), axonal damage (MESH:D001480), facial palsy (MESH:D005158), myokymia (MESH:D020385), Arsenic poisoning (MESH:D020261), neuropathic pain (MESH:D009437), Campylobacter jejuni infection (MESH:D002169), axonal degeneration (MESH:D009410), sensory loss (MESH:C580162), AIPN (MESH:D010523), motor or sensory deficits (MESH:D001289), foot hyperkeratosis (MESH:D005530), toxicity (MESH:D064420), numbness (MESH:D006987), Heavy metal poisoning (MESH:D000075322), nerve damage (MESH:D000080902), demyelinating (MESH:D003711)
- **Chemicals:** glycyrrhizin (MESH:D019695), Methylprednisolone (MESH:D008775), ADP (MESH:D000244), metal (MESH:D008670), Arsenic (MESH:D001151), mecobalamin (MESH:C019476), ATP (MESH:D000255), Vitamin B1 (MESH:D013831), sulfhydryl (MESH:D013438), sulfatide (MESH:D013433), Sodium thiosulfate (MESH:C017717), AIPN (-), ganglioside (MESH:D005732)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12916063/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916063/full.md

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Source: https://tomesphere.com/paper/PMC12916063