Erkan Serkan, Yabanoglu Hakan, Avci Tevfik, Dogan Durdag Gulsen, Bolat Filiz, Emrah Kocer Nazim
Department of General Surgery, Baskent University, Adana Dr. Turgut Noyan Application and Research Center, Adana, Türkiye.
Department of Gynecology and Obstetrics, Baskent University, Adana Dr. Turgut Noyan Application and Research Center, Adana, Türkiye.
Sisli Etfal Hastan Tip Bul. 2024 Sep 30;58(3):284-290. doi: 10.14744/SEMB.2024.90248. eCollection 2024.
Struma ovarii (SO) accounts for approximately 1% of all ovarian tumors. The objective of our study is to contribute to the treatment algorithm by presenting our clinical experience in a comprehensive case series of patients diagnosed with SO, predominantly characterized by thyroid tissue within a monodermal teratoma.
Patients aged 17 years and older who underwent surgery due to ovarian masses and were histopathologically diagnosed with SO between January 2012 and January 2022 were included in the study. The patients' files were retrospectively reviewed. Demographic data, presenting complaints, radiological findings, tumor sizes, laboratory data, surgical procedures performed, pathology reports, additional treatments, and follow-up information were recorded.
The median age of total 19 patients was 41.7 (17-74) years. Among them, malignant struma ovarii was present in 3 patients. In patients with histopathologically confirmed benign struma ovarii, no additional treatment was administered after tumor enucleation. In malignant cases, in addition to unilateral salpingo-oophorectomy, total thyroidectomy, radioactive iodine (RAI) ablation, and L-Thyroxine suppression were performed. No mortality occurred during the follow-up period.
Although conservative treatments are considered acceptable treatment in cases of benign struma ovarii, the management of cases with malignant struma ovarii is controversial. Fertility-sparing surgery followed by postoperative adjuvant thyroidectomy and radioactive iodine ablation may be preferred for young women.
卵巢甲状腺肿(SO)约占所有卵巢肿瘤的1%。我们研究的目的是通过展示我们在一系列经病理确诊为SO患者中的临床经验,为治疗方案提供参考,这些患者主要表现为单胚层畸胎瘤内含有甲状腺组织。
纳入2012年1月至2022年1月期间因卵巢肿块接受手术且经组织病理学诊断为SO的17岁及以上患者。对患者病历进行回顾性分析。记录人口统计学数据、主诉、影像学检查结果、肿瘤大小、实验室数据、手术方式、病理报告、额外治疗及随访信息。
19例患者的中位年龄为41.7(17 - 74)岁。其中,3例为恶性卵巢甲状腺肿。组织病理学确诊为良性卵巢甲状腺肿的患者,肿瘤剜除术后未给予额外治疗。恶性病例除行单侧输卵管卵巢切除术外,还进行了全甲状腺切除术、放射性碘(RAI)消融及左甲状腺素抑制治疗。随访期间无死亡病例。
虽然对于良性卵巢甲状腺肿病例,保守治疗被认为是可接受的治疗方法,但恶性卵巢甲状腺肿病例的治疗仍存在争议。对于年轻女性,保留生育功能手术联合术后辅助甲状腺切除术及放射性碘消融可能是更好的选择。