Evidence map›Paper›PMID 39618593›Full record

ArticleCureus2024

Sclerosing Mucoepidermoid Carcinoma With Eosinophilia of the Thyroid: A Rare Case From Georgia and a Comprehensive Literature Review.

Giorgi Akhvlediani, Elene Dzodzuashvili, Nino Gabidzashvili, Bakur Arabuli, Keti Tsomaia, Mikheil Jangavadze

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In one paragraph

Article in Cureus, 2024. 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

6 authors.

Giorgi AkhvledianiDepartment of Endocrinology, American Hospital Tbilisi, Tbilisi, GEO.
Elene DzodzuashviliDepartment of Endocrinology, American Hospital Tbilisi, Tbilisi, GEO.
Nino GabidzashviliDepartment of Endocrinology, American Hospital Tbilisi, Tbilisi, GEO.
Bakur ArabuliDepartment of General and Endocrine Surgery, American Hospital Tbilisi, Tbilisi, GEO.
Keti TsomaiaAleksandre Natishvili Institute of Morphology, Ivane Javakhishvili Tbilisi State University, Tbilisi, GEO.
Mikheil JangavadzeDepartment of Pathology and Forensic Medicine, Faculty of Medicine, Ivane Javakhishvili Tbilisi State University, Tbilisi, GEO.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sclerosing mucoepidermoid carcinoma with eosinophilia (SMECE) is a rare thyroid malignancy typically linked to chronic lymphocytic thyroiditis. We present the first documented case of SMECE in Georgia, involving a 41-year-old woman with Hashimoto's thyroiditis. A 16 mm hypoechoic thyroid nodule was detected on routine ultrasound, and fine needle aspiration categorized it as Bethesda V. The patient underwent total thyroidectomy with central neck dissection, confirming SMECE confined to the thyroid without lymph node involvement (0/22 nodes). She recovered well postoperatively on hormone replacement therapy, with no recurrence during follow-up. This case emphasizes the importance of considering SMECE in patients with thyroid nodules, especially with autoimmune thyroiditis. Key diagnostic features include eosinophilic infiltration in a sclerotic stroma and mucinous and squamous differentiation. Immunohistochemistry, showing positivity for CK7, p63, and CEA, was critical for diagnosis. Given the absence of extrathyroidal spread, the patient did not receive radioactive iodine (RAI) therapy. This report adds to the limited literature, underscoring the need for careful histopathological and immunohistochemical evaluation in rare thyroid malignancies.

Indexed as

chronic lymphocytic thyroiditisgeorgiahistopathologysclerosing mucoepidermoid carcinoma with eosinophilia (smece)thyroid gland neoplasm

Identifiers

PMID39618593
PMCPMC11607140

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