Akhvlediani Giorgi, Dzodzuashvili Elene, Gabidzashvili Nino, Arabuli Bakur, Tsomaia Keti, Jangavadze Mikheil
Department of Endocrinology, American Hospital Tbilisi, Tbilisi, GEO.
Department of Internal Medicine, Tbilisi State Medical University, Tbilisi, GEO.
Cureus. 2024 Oct 30;16(10):e72739. doi: 10.7759/cureus.72739. eCollection 2024 Oct.
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.
伴有嗜酸性粒细胞增多的硬化性黏液表皮样癌(SMECE)是一种罕见的甲状腺恶性肿瘤,通常与慢性淋巴细胞性甲状腺炎有关。我们报告了格鲁吉亚首例有记录的SMECE病例,患者为一名患有桥本甲状腺炎的41岁女性。常规超声检查发现一个16毫米的甲状腺低回声结节,细针穿刺将其分类为贝塞斯达Ⅴ类。患者接受了全甲状腺切除术及中央区颈淋巴结清扫术,证实SMECE局限于甲状腺,无淋巴结受累(22个淋巴结均为阴性)。术后她在激素替代治疗下恢复良好,随访期间无复发。该病例强调了在甲状腺结节患者中,尤其是伴有自身免疫性甲状腺炎的患者中考虑SMECE的重要性。关键诊断特征包括硬化性间质中的嗜酸性粒细胞浸润以及黏液样和鳞状分化。免疫组化显示CK7、p63和CEA呈阳性,对诊断至关重要。鉴于无甲状腺外扩散,患者未接受放射性碘(RAI)治疗。本报告补充了有限的文献资料,强调了对罕见甲状腺恶性肿瘤进行仔细的组织病理学和免疫组化评估的必要性。