# Late Recurrence of Graves’ Hyperthyroidism With Thyroid Eye Disease Approximately Five Decades After Radioiodine Ablation: A Rare Clinical Scenario

**Authors:** Saraswathi Saiprasad, Narayana Swamy, Sriharika Gottipolu, Theresa Cao

PMC · DOI: 10.7759/cureus.103975 · Cureus · 2026-02-20

## TL;DR

A rare case of Graves’ disease recurrence with thyroid eye disease and osteoporosis is reported decades after radioiodine treatment.

## Contribution

This paper presents a rare clinical case of late recurrence of Graves’ hyperthyroidism after radioiodine ablation.

## Key findings

- A woman in her late 60s developed recurrent hyperthyroidism decades after RAI treatment.
- Thyroid autoantibody testing confirmed Graves’ disease recurrence despite prior hypothyroidism.
- The case emphasizes the need to consider endogenous causes in post-ablative thyrotoxicosis.

## Abstract

Radioiodine ablation (RAI) is widely regarded as definitive therapy for Graves’ disease and typically results in permanent hypothyroidism requiring lifelong thyroid hormone replacement. True recurrence of Graves’ hyperthyroidism after a prolonged post-ablative hypothyroid phase is rare and may be misinterpreted as iatrogenic thyrotoxicosis from exogenous hormone excess. We report the case of a woman in her late 60s with Graves’ disease treated with RAI in early adulthood, followed by several decades of stable hypothyroidism managed with levothyroxine, who later developed recurrent endogenous hyperthyroidism complicated by thyroid eye disease and osteoporosis. Serial thyroid function testing demonstrated persistent thyrotoxicosis despite progressive levothyroxine dose reduction and eventual discontinuation. In patients receiving thyroid hormone replacement therapy, biochemical hyperthyroidism is most commonly iatrogenic and typically resolves with dose reduction or hormone withdrawal; however, in this case, biochemical hyperthyroidism failed to recover as expected following complete discontinuation of levothyroxine, prompting further evaluation for endogenous causes of hyperthyroidism. Subsequent autoimmune testing revealed markedly elevated thyrotropin receptor antibodies and thyroid-stimulating immunoglobulins, confirming recurrent Graves’ disease. This case highlights the importance of considering endogenous hyperthyroidism in post-ablative hypothyroid patients receiving thyroid hormone replacement therapy who exhibit persistent biochemical thyrotoxicosis despite dose reduction and discontinuation, and underscores the diagnostic value of thyroid autoantibody testing in conjunction with clinical presentation in establishing disease recurrence.

## Linked entities

- **Chemicals:** levothyroxine (PubChem CID 5819)
- **Diseases:** Graves’ disease (MONDO:0005364), thyroid eye disease (MONDO:0001509), osteoporosis (MONDO:0005298)

## Full-text entities

- **Genes:** TSHR (thyroid stimulating hormone receptor) [NCBI Gene 7253] {aka CHNG1, LGR3, hTSHR-I}
- **Diseases:** Thyroid Eye Disease (MESH:D049970), Graves' Hyperthyroidism (MESH:D006980), thyrotoxicosis (MESH:C566386), hypothyroid (MESH:D007037), osteoporosis (MESH:D010024), Graves' disease (MESH:D006111)
- **Chemicals:** Radioiodine (MESH:C000614965), levothyroxine (MESH:D013974)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13006052/full.md

## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC13006052/full.md

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Source: https://tomesphere.com/paper/PMC13006052