# Late-Onset Autoimmune Myasthenia Gravis: A Diagnosis Not to Be Overlooked in the Elderly

**Authors:** Abrar-Ahmad Zulfiqar

PMC · DOI: 10.7759/cureus.82707 · Cureus · 2025-04-21

## TL;DR

This paper discusses a case of late-onset autoimmune myasthenia gravis in an elderly patient, emphasizing the importance of timely diagnosis and treatment for better outcomes.

## Contribution

The paper presents a case study highlighting the atypical presentation and management challenges of late-onset myasthenia gravis in the elderly.

## Key findings

- Late-onset autoimmune myasthenia gravis can present with fluctuating symptoms like ptosis in elderly patients.
- Management with immunoglobulins and immunosuppressive therapy can stabilize disease progression in elderly patients.
- Early diagnosis and treatment are crucial for improving prognosis in geriatric populations.

## Abstract

Autoimmune myasthenia gravis is a rare neuromuscular disorder of autoimmune origin, characterized by fluctuating muscle weakness. Although it classically occurs in young adults, late onset in the elderly is possible, often with atypical presentations that may delay diagnosis. We report the case of an 81-year-old female patient who initially consulted us with fluctuating right ptosis, in the absence of other neurological signs. Biological workup revealed the presence of anti-acetylcholine receptor (anti-AChR) antibodies, confirming the diagnosis of autoimmune myasthenia gravis. Thoracic imaging revealed no thymoma. Anticholinesterase therapy was initiated with partial improvement, followed by clinical progression two years later to bulbar involvement (dysarthria, swallowing disorders). Management involved the administration of intravenous immunoglobulins, with a favorable clinical response. Corticosteroid therapy was then introduced, together with azathioprine immunosuppressive therapy, stabilizing the course. This case illustrates the importance of considering the diagnosis of myasthenia gravis, even at an advanced age, in the face of fluctuating or unusual signs. It also highlights the diagnostic and therapeutic challenges specific to the geriatric population, particularly in relation to comorbidities, adverse drug reactions, and the need for multidisciplinary follow-up. Early recognition and treatment of the disease can significantly improve prognosis and quality of life.

## Linked entities

- **Chemicals:** azathioprine (PubChem CID 2265)
- **Diseases:** autoimmune myasthenia gravis (MONDO:0009688)

## Full-text entities

- **Diseases:** thymoma (MESH:D013945), swallowing disorders (MESH:D003680), muscle weakness (MESH:D018908), Autoimmune Myasthenia Gravis (MESH:D020720), ptosis (MESH:C564553), myasthenia gravis (MESH:D009157), neuromuscular disorder (MESH:D009468), dysarthria (MESH:D004401)
- **Chemicals:** azathioprine (MESH:D001379)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC12094810/full.md

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Source: https://tomesphere.com/paper/PMC12094810