Jelena Roganović, Željana Jotanović Pahović, Alex Anton Bruno Lozić, Irena Seili Bekafigo
{"title":"Spindle Epithelial Tumor with Thymus-like Element (SETTLE): A Case Report","authors":"Jelena Roganović, Željana Jotanović Pahović, Alex Anton Bruno Lozić, Irena Seili Bekafigo","doi":"10.5457/p2005-114.363","DOIUrl":null,"url":null,"abstract":"Objective – Spindle epithelial tumor with thymus-like element (SETTLE) is an extremely rare neoplasm of the thyroid gland. We present the first case of SETTLE in Croatia.Case Report – A 17-year-old girl with Hashimoto’s thyroiditis was presented with an asymptomatic solitary thyroid nodule. Fine-needle aspiration cytology was suggestive of SETTLE. The patient underwent hemithyroidectomy and immunohistopathology confirmed the diagnosis. There is no evidence of local or distant disease recur- rence at 8 years after surgery. Conclusion – SETTLE should be included in the differential diagnosis of thyroid gland tumors in children and adolescents. Surgical resection is the mainstay of treatment. Due to possible late metastases, a close and long-term follow-up is recommended. ","PeriodicalId":36516,"journal":{"name":"Central European Journal of Paediatrics","volume":"35 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Central European Journal of Paediatrics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5457/p2005-114.363","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Objective – Spindle epithelial tumor with thymus-like element (SETTLE) is an extremely rare neoplasm of the thyroid gland. We present the first case of SETTLE in Croatia.Case Report – A 17-year-old girl with Hashimoto’s thyroiditis was presented with an asymptomatic solitary thyroid nodule. Fine-needle aspiration cytology was suggestive of SETTLE. The patient underwent hemithyroidectomy and immunohistopathology confirmed the diagnosis. There is no evidence of local or distant disease recur- rence at 8 years after surgery. Conclusion – SETTLE should be included in the differential diagnosis of thyroid gland tumors in children and adolescents. Surgical resection is the mainstay of treatment. Due to possible late metastases, a close and long-term follow-up is recommended.