Evidence map›Paper›PMID 40201472›Full record

ArticleAACE clinical case reports

Mild Thyrotoxicosis due to Seronegative Graves' Disease or Disseminated Thyroid Autonomy.

Gael Charbonne, Fatima Hallak, Alma Elizabeth Rivera Cruz, Stephen Devitt McDonald

Abstract readCase Reports
In one paragraph

Article in AACE clinical case reports. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Gael CharbonneKettering Health Main Campus, Department of Internal Medicine, Kettering, Ohio.
Fatima HallakKettering Health Main Campus, Department of Internal Medicine, Kettering, Ohio.
Alma Elizabeth Rivera CruzKettering Health Main Campus, Department of Internal Medicine, Kettering, Ohio.
Stephen Devitt McDonaldKettering Health Miamisburg, Internal Medicine Clinic, Miamisburg, Ohio.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Objective: Disseminated thyroid autonomy (DTA) and seronegative Graves' disease are rare causes of hyperthyroidism with similar clinical presentations. This case report highlights the diagnostic challenges between these entities. Case Presentation: A 35-year-old male presented with palpitations, diaphoresis, and a small goiter. His TSH was 0.249 mIU/L (reference: 0.45-4.5 mIU/L) and free T4 was 3.0 ng/dL (reference: 0.88-1.77 ng/dL). Thyroid peroxidase antibodies, TRAb, and TSI were repeatedly negative. Ultrasound showed a diffusely enlarged thyroid, and radioactive iodine uptake was 35% (reference: 10% to 35%) with thyroid scintigraphy revealing diffusely increased uptake, indicating a hyperfunctioning thyroid without nodules. Treatment with Methimazole 5 mg daily resolved symptoms within 6 months. Discussion: Thyroid biopsy can help distinguish DTA from seronegative Graves disease. DTA is marked by nodular hyperplasia without lymphocytic infiltration, indicating a non-autoimmune nature, while seronegative Graves' disease exhibits diffuse follicular hyperplasia with lymphocytic infiltration, just as typical Graves' disease despite undetectable autoatibodies. The possibility of false-negative TRAb results complicates diagnosis, with up to 22% of patients initially diagnosed with DTA later testing TRAb-positive upon retesting. Some cases of DTA may involve TSH receptor gene mutations. Conclusion: This case highlights the complexity of distinguishing DTA, seronegative Graves' disease and typical Graves' disease with initial false negative testing. A systematic approach with repeat testing and, when feasible, biopsy, is critical to distinguish these entities. Further studies with histologic analysis are needed to clarify outcomes and develop tailored managements, as these conditions have different remission rates and are driven by different mechanisms.

Indexed as

disseminated thyroid autonomyGraves’ diseasenonautoimmune hyperthyroidismseronegative Graves’ disease

Identifiers

PMID40201472
PMCPMC11973595

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