Evidence map›Paper›PMID 37497347›Full record

ReviewFrontiers in endocrinology2023

Warthin-like papillary thyroid carcinoma: a case report and comprehensive review of the literature.

Abdel Mouhaymen Missaoui, Fatma Hamza, Wafa Belabed, Manel Mellouli, Mohamed Maaloul, Slim Charfi, Issam Jardak, Tahya Sellami-Boudawara, Nabila Rekik, Mohamed Abid

Open access · goldAbstract readCase ReportsReview
In one paragraph

Review in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
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

10 authors at 3 institutions in 1 country.

Abdel Mouhaymen MissaouiDepartment of Endocrinology and Diabetology, Hedi Chaker University Hospital, Sfax, Tunisia.
Fatma HamzaFaculty of Medicine of Sfax, University of Sfax, Sfax, Tunisia.
Wafa BelabedDepartment of Endocrinology and Diabetology, Hedi Chaker University Hospital, Sfax, Tunisia.
Manel MellouliFaculty of Medicine of Sfax, University of Sfax, Sfax, Tunisia.
Mohamed MaaloulFaculty of Medicine of Sfax, University of Sfax, Sfax, Tunisia.
Slim CharfiFaculty of Medicine of Sfax, University of Sfax, Sfax, Tunisia.
Issam JardakFaculty of Medicine of Sfax, University of Sfax, Sfax, Tunisia.
Tahya Sellami-BoudawaraFaculty of Medicine of Sfax, University of Sfax, Sfax, Tunisia.
Nabila RekikDepartment of Endocrinology and Diabetology, Hedi Chaker University Hospital, Sfax, Tunisia.
Mohamed AbidDepartment of Endocrinology and Diabetology, Hedi Chaker University Hospital, Sfax, Tunisia.
University of Sfax · TNHopital Universitaire Habib Bourguiba · TNHopital Universitaire Hedi Chaker · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Papillary Thyroid Carcinoma (PTC) is the most frequent endocrine malignancy with a variety of histological presentations. Warthin-like Papillary Thyroid Carcinoma (WLPTC) is an uncommon neoplasm that is recognized as a distinct subtype of PTC in the WHO classification of thyroid tumors. In this report, we present a novel case of WLPTC in a female patient and provide an in-depth review of the available literature on its clinical, pathological, and therapeutic characteristics. Case presentation: A 27-year-old female patient was referred for neck swelling. Ultrasound showed two suspicious thyroid nodules leading to a thyroidectomy. She was diagnosed with intermediate-risk bifocal foci of classic PTC and WLPTC, arising from a background of chronic lymphocytic thyroiditis (CLT). This pT1b(m) N1b M0 malignancy was treated with adjuvant isotopic ablation and suppressive thyroxine therapy. The 1-year outcomes were favorable. Literature review: It covered articles published from 1995 to 2022, by searching PubMed and Google Scholar using specific terms. Out of 148 articles reviewed by two authors, 25 relevant articles were selected, including 13 case reports and 12 case series. The study included 150 cases of WLPTC. Data related to clinical presentation, imaging, histological features, management, and outcomes, were extracted. The mean age of diagnosis was 39 years, with a female predominance. The most common clinical presentation was neck swelling. Thyroid autoimmunity was positive in 71.6% of patients. Lymph node metastases were present in 28% of cases, with no reported distant metastases. Overall, the outcomes were favorable. Conclusion: WLPTC shares similar clinical and radiological presentations as classic PTC. The hallmark histological features of WLPTC are papillae lined with oncocytic tumor cells with papillary nuclear changes and lymphoid stroma. WLPTC is almost constantly associated with CLT. The management of WLPTC aligns with that of classic PTC with comparable stage and risk category, often resulting in favorable outcomes.

Indexed as

CarcinomaCarcinoma, PapillaryHashimoto DiseaseThyroid NeoplasmsAdultFemaleHumansMaleThyroid Cancer, Papillarycase reportchronic lymphocytic thyroiditispapillary thyroid carcinomareview of the literaturethyroid neoplasmsthyroid nodulewarthin-like papillary thyroid carcinoma

Identifiers

PMID37497347
PMCPMC10367547
OpenAlexW4383957129

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.