# Peripartum Management of Refractory Graves’ Thyrotoxicosis

**Authors:** Sonam Tshering, Ashutosh Kapoor, Sophie Buckley, Fareeha Rizvi

PMC · DOI: 10.7759/cureus.102213 · Cureus · 2026-01-24

## TL;DR

This paper discusses the challenges of managing severe Graves’ disease during and after pregnancy when standard treatments fail.

## Contribution

The paper presents a rare case of refractory Graves’ thyrotoxicosis managed with radioiodine therapy during the peripartum period.

## Key findings

- The patient remained hyperthyroid despite high-dose PTU during pregnancy.
- Radioiodine therapy was used successfully but relapse occurred later.
- Multidisciplinary care is essential for managing high-risk cases.

## Abstract

Graves’ disease (GD) is the most common cause of hyperthyroidism, characterized by autoimmune stimulation of the thyroid gland and typically managed with antithyroid drugs (ATDs), radioiodine (RAI) therapy, or surgery. While most patients respond to standard antithyroid therapy, a minority exhibit refractory thyrotoxicosis, posing significant clinical challenges. Pregnancy further complicates management due to immunological shifts, increased risk of adverse maternal and fetal outcomes, and limitations in therapeutic options. We present the case of a 39-year-old woman with severe, persistent Graves’ thyrotoxicosis refractory to high-dose propylthiouracil (PTU), whose clinical course was complicated by pregnancy and postpartum deterioration. Despite management with adequate doses of PTU, she remained biochemically hyperthyroid throughout pregnancy, developed gestational hypertension, and delivered a baby with a cleft palate. Postpartum, she suffered from depression and further deterioration of her thyrotoxicosis, with laboratory evidence of markedly elevated thyroid hormones and thyroid-stimulating hormone (TSH) receptor antibodies, despite directly observed high-dose PTU therapy. Definitive management options were limited by a highly vascular thyroid gland, significant myopathy, intolerance to cholestyramine, and psychiatric comorbidities. Surgery was deemed high risk, and RAI therapy was ultimately chosen, with careful pre- and post-treatment using high-dose propranolol to mitigate the risk of thyroid storm. The patient tolerated RAI without major complications and achieved euthyroidism at six months post-treatment, but relapsed at nine months, which may have been influenced by factors such as the long delay between diagnosis and RAI therapy, the presence of a large goiter, and the inability to achieve normal thyroid levels before treatment. This case emphasizes the complexities of managing refractory Graves’ thyrotoxicosis in the peripartum period, particularly when conventional therapies fail, and definitive interventions carry elevated risk. It also highlights the importance of a multidisciplinary, patient-centered approach and the need for individualized management strategies in challenging clinical scenarios.

## Linked entities

- **Chemicals:** propylthiouracil (PubChem CID 657298), propranolol (PubChem CID 4946)
- **Diseases:** Graves’ disease (MONDO:0005364), hyperthyroidism (MONDO:0004425), gestational hypertension (MONDO:0024664), depression (MONDO:0002050), myopathy (MONDO:0005336), cleft palate (MONDO:0016064)

## Full-text entities

- **Genes:** ATD (asphixiating thoracic dystrophy (chondroectodermal dysplasia-like syndrome)) [NCBI Gene 465] {aka ATD1}, TPO (thyroid peroxidase) [NCBI Gene 7173] {aka MSA, TDH2A, TPX}, TSHR (thyroid stimulating hormone receptor) [NCBI Gene 7253] {aka CHNG1, LGR3, hTSHR-I}
- **Diseases:** abdominal wall defects (MESH:D046449), malabsorption (MESH:D008286), tremor (MESH:D014202), Thyroid storm (MESH:D013958), ectopic pregnancy (MESH:D011271), congenital anomalies (MESH:D000013), intrauterine growth restriction (MESH:D005317), omphalocele (MESH:D006554), weight loss (MESH:D015431), gastrointestinal side effects (MESH:D064420), postpartum depression (MESH:D019052), osteoporosis (MESH:D010024), anxiety (MESH:D001007), Psychiatric comorbidity (MESH:D001523), preterm delivery (MESH:D047928), nodular goiter (MESH:D006044), choanal and esophageal atresia (MESH:D002754), cardiovascular collapse and death (MESH:D002318), cleft palate (MESH:D002972), gestational hypertension (MESH:D046110), insomnia (MESH:D007319), iodine deficiency (MESH:D003409), Graves' ophthalmopathy (MESH:D049970), atrial fibrillation (MESH:D001281), muscle weakness (MESH:D018908), gastrointestinal intolerance (MESH:D005767), endocrine disease (MESH:D004700), thyroid hormone excess (MESH:C531600), mitral (MESH:D008946), fatigue (MESH:D005221), myopathy (MESH:D009135), thyrotoxicosis (MESH:C566386), Graves' hyperthyroidism (MESH:D006980), liver failure (MESH:D017093), palpitations (MESH:D006331), embolic events (MESH:D004617), ATDs (MESH:D000081015), mood impairment (MESH:D019964), stillbirth (MESH:D050497), Diffuse thyroid enlargement (MESH:D013959), nausea and (MESH:D009325), autoimmune (MESH:D001327), heart failure (MESH:D006333), atrial dilation (MESH:C563984), miscarriage (MESH:D000022), aplasia cutis (MESH:D004476), tachycardia (MESH:D013610), depression (MESH:D003866), tricuspid regurgitation (MESH:D014262), celiac disease (MESH:D002446), GD (MESH:D006111), pulmonary hypertension (MESH:D006976), vomiting (MESH:D014839), Thyroid dermopathy (MESH:D013966), proptosis (MESH:D005094), goiter (MESH:D006042)
- **Chemicals:** Cholestyramine (MESH:D002792), T4 (MESH:D013974), antithyroid (-), carbimazole (MESH:D002231), sertraline (MESH:D020280), Propranolol (MESH:D011433), I-131 (MESH:C000614965), N (MESH:D009584), iron (MESH:D007501), vitamin B12 (MESH:D014805), iodine (MESH:D007455), PTU (MESH:D011441), TDS (MESH:C076628), Steroids (MESH:D013256), Methimazole (MESH:D008713), folate (MESH:D005492), T3 (MESH:D014284)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12928177/full.md

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Source: https://tomesphere.com/paper/PMC12928177