Evidence map›Paper›PMID 41699545›Full record

ArticleBMC surgery2026

Papillary thyroid carcinoma in graves' disease: prevalence, clinicopathological features, and preoperative predictors.

Tugba Matlim Ozel, Mine Yilmaz, Sezer Akbulut, Aykut Celik, Gorkem Yildiz, Nilsen Erdogan, Serkan Sari

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Article in BMC surgery, 2026. 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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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Tugba Matlim OzelDepartment of General Surgery, Division of Endocrine Surgery, University of Health Sciences Turkey, Basaksehir Cam and Sakura City Hospital, Istanbul, Turkey. tugbamatlim79@gmail.com.
Mine YilmazDepartment of General Surgery, Division of Endocrine Surgery, University of Health Sciences Turkey, Basaksehir Cam and Sakura City Hospital, Istanbul, Turkey.
Sezer AkbulutDepartment of General Surgery, Division of Endocrine Surgery, University of Health Sciences Turkey, Basaksehir Cam and Sakura City Hospital, Istanbul, Turkey.
Aykut CelikDepartment of General Surgery, Division of Endocrine Surgery, University of Health Sciences Turkey, Basaksehir Cam and Sakura City Hospital, Istanbul, Turkey.
Gorkem YildizDepartment of General Surgery, Division of Endocrine Surgery, University of Health Sciences Turkey, Basaksehir Cam and Sakura City Hospital, Istanbul, Turkey.
Nilsen ErdoganDepartment of Pathology, University of Health Sciences Turkey, Basaksehir Cam and Sakura City Hospital, Istanbul, Turkey.
Serkan SariDepartment of General Surgery, Division of Endocrine Surgery, University of Health Sciences Turkey, Basaksehir Cam and Sakura City Hospital, Istanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe coexistence of Graves' disease (GD) and papillary thyroid carcinoma (PTC) remains a subject of clinical debate. While PTC is frequently detected incidentally after thyroidectomy for GD, its prevalence, clinicopathological behavior, and preoperative predictors remain insufficiently defined.

methodsThis single-center retrospective cohort study included 602 patients who underwent thyroidectomy between 2020 and 2025. Patients were categorized as: GD + PTC (n = 51); GD-only (n = 109); and PTC-only (n = 442). Demographic, biochemical, radiological, surgical, and pathological data were analyzed. Univariate and multivariate logistic regression models were used to identify factors associated with PTC development in GD.

resultsThe prevalence of PTC among GD patients was 31.9%. Compared with sporadic PTC, GD-associated tumors were smaller (median 5 mm vs. 12 mm, p < 0.001) and demonstrated fewer aggressive features including lymphatic invasion, capsular invasion, multifocality, bilaterality, and nodal metastasis (all p < 0.01). GD + PTC patients were younger and showed a lower female predominance than those with sporadic PTC. When compared with GD-only patients, the GD + PTC group had significantly lower thyroid-stimulating Immunoglobulin (TSI) titers (median 3.8 vs. 7.65 IU/L, p = 0.007) and a higher prevalence of ultrasound-detected thyroid nodules (64.7% vs. 27.5%, p < 0.001). In multivariate analysis, only US-detected nodules (OR 3.56, p = 0.003) and lower TSI levels (OR 0.95, p = 0.03) independently predicted PTC in GD.

conclusionPTC is relatively common among surgically treated GD patients, yet presents predominantly as microcarcinoma with less aggressive histopathological features. The presence of ultrasound-detected thyroid nodules was the strongest preoperative predictor of malignancy. These findings support careful and systematic ultrasonographic assessment in patients with GD, with FNAB guided by established ultrasound risk patterns, nodule size thresholds, and high-risk clinical features, rather than indiscriminate lowering of biopsy thresholds.

Indexed as

Graves DiseaseThyroid Cancer, PapillaryThyroid NeoplasmsAdultFemaleHumansMaleMiddle AgedPrevalenceRetrospective StudiesThyroidectomyGraves diseasePapillary thyroid cancerThyroidectomyThyroid-stimulating immunoglobulin (TSI)

Identifiers

PMID41699545
PMCPMC12980858

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