Evidence map›Paper›PMID 42559157›Full record

ArticleCase reports in endocrinology2026

Alemtuzumab-Induced Graves' Disease Complicated by Pretibial Myxoedema: A Case Report.

Aongus O'Brolchain, Elham Reda

Abstract read
In one paragraph

Article in Case reports in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Aongus O'BrolchainDepartment of Endocrinology, Gold Coast University Hospital, Southport, Queensland, Australia, qld.gov.au.ORCID https://orcid.org/0009-0006-8753-6386
Elham RedaDepartment of Endocrinology, Gold Coast University Hospital, Southport, Queensland, Australia, qld.gov.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Alemtuzumab, a monoclonal antibody targeting CD52, is associated with a high incidence of secondary autoimmune disease, most commonly thyroid dysfunction. Alemtuzumab-induced Graves' disease (AIGD) typically follows a relapsing course and may exhibit atypical or severe phenotypes during immune reconstitution (IR). Case Presentation: We report a case of severe thyrotoxicosis following alemtuzumab therapy for multiple sclerosis, complicated by the development of thyroid eye disease (TED) and pretibial myxoedema (PTM). Despite escalation of antithyroid therapy, biochemical and clinical control remained suboptimal. Radioiodine therapy was not pursued due to the presence of established orbitopathy. Given persistent severe disease and extrathyroidal manifestations, definitive management with total thyroidectomy was undertaken. Results: Thyroidectomy resulted in rapid biochemical control of thyrotoxicosis. thyroid-stimulating hormone-receptor antibody (TRAb) remained markedly elevated after thyroidectomy, indicating persistent autoimmune activity despite removal of the thyroid gland. Conclusion: This case highlights an aggressive and uncommon presentation of AIGD characterised by severe thyrotoxicosis, orbitopathy and PTM. Clinicians should recognise the potential for atypical and refractory disease following alemtuzumab therapy. In selected cases, early consideration of definitive therapy is warranted, particularly when radioiodine is considered unsuitable.

Indexed as

alemtuzumabGravespretibial myxoedema

Identifiers

PMID42559157
PMCPMC13439395

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