# Type 2 Respiratory Failure as an Initial Manifestation of Lambert–Eaton Myasthenic Syndrome Complicated by Paraneoplastic Autoimmune Encephalitis

**Authors:** Sota Uemura, Satoru Fujiwara, Tsuyoshi Sasada, Nobuo Kohara, Michi Kawamoto

PMC · DOI: 10.7759/cureus.78284 · 2025-01-31

## TL;DR

A rare case where a neurological disorder caused by cancer first showed as severe breathing failure.

## Contribution

Highlights atypical presentation of LEMS with respiratory failure and coexisting autoimmune encephalitis.

## Key findings

- LEMS was diagnosed via nerve conduction studies after initial respiratory failure.
- Coexisting autoimmune encephalitis was confirmed with antibody testing.
- Underlying small-cell lung cancer was identified but untreated due to patient choice.

## Abstract

Lambert-Eaton myasthenic syndrome (LEMS) is a paraneoplastic or autoimmune neuromuscular disorder that typically presents with limb weakness or autonomic dysfunction. Here, we report a rare case of LEMS with acute type 2 respiratory failure as the initial symptom. A 79-year-old woman was admitted with acute disturbance of consciousness and type 2 respiratory failure. On admission, she presented with confusion, seizures, and respiratory acidosis requiring non-invasive positive pressure ventilation. Cerebrospinal fluid analysis revealed pleocytosis and elevated protein levels without infection. Electroencephalography showed nonspecific slowing, while imaging revealed no abnormalities. A nerve conduction study on day 10 confirmed LEMS, with findings of low-amplitude compound motor action potentials and facilitation on high-frequency stimulation. Coexisting autoimmune encephalitis was diagnosed based on clinical presentation and serum antibody positivity for voltage-gated calcium channels and gamma-aminobutyric acid B receptors. Positron emission tomography/CT identified small-cell lung cancer, confirmed by biopsy. The patient and family declined invasive cancer therapies. Then, the patient passed away on day 60.

This case highlights the diagnostic challenge of atypical presentations of paraneoplastic neurological syndromes, including LEMS and autoimmune encephalitis. Early recognition of LEMS in patients with unexplained type 2 respiratory failure through nerve conduction studies is critical. This report underscores the importance of considering paraneoplastic etiologies in patients with multiple neurological syndromes.

## Linked entities

- **Diseases:** Lambert–Eaton myasthenic syndrome (MONDO:0018556), small-cell lung cancer (MONDO:0008433)

## Full-text entities

- **Diseases:** seizures (MESH:D012640), acute disturbance of consciousness (MESH:D003244), autoimmune neuromuscular disorder (MESH:D009468), paraneoplastic neurological syndromes (MESH:D020361), Paraneoplastic Autoimmune Encephalitis (MESH:D020274), respiratory acidosis (MESH:D000142), cancer (MESH:D009369), limb weakness (MESH:D018908), small-cell lung cancer (MESH:D055752), Type 2 Respiratory Failure (MESH:D012131), infection (MESH:D007239), pleocytosis (MESH:D007964), paraneoplastic (MESH:D010257), confusion (MESH:D003221), autonomic dysfunction (MESH:D001342), neurological syndromes (MESH:D009461), LEMS (MESH:D015624)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11872067/full.md

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Source: https://tomesphere.com/paper/PMC11872067