Mesquita Juliana Bezerra, Biscolla Rosa Paula M
Liga Norte Riograndense Contra o Cancer, Natal, Brazil.
Thyroid Diseases Center and Laboratory of Molecular and Translational Endocrinology, Division of Endocrinology, Department of Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.
Endocrinol Diabetes Metab Case Rep. 2024 Oct 3;2024(4). doi: 10.1530/EDM-24-0082. Print 2024 Oct 1.
Thyroid carcinoma originating in Struma Ovarii (SO) is a rare thyroid ectopic cancer that accounts for 0.01% of all ovarian malignancies and is associated with hyperthyroidism in less than 15% of cases. In a 44-year-old patient with pelvic pain, the CT scan revealed a solid-cystic formation in the ovarium. A left oophorectomy was performed and showed a borderline serous tumor and papillary thyroid carcinoma ('thyroid carcinoma originating in Struma Ovarii') measuring 10 cm. Thyroid function was assessed, and hyperthyroidism was diagnosed. Surgical complementation and a pelvic re-approach were performed. The histological findings showed a papillary thyroid carcinoma in the uterine serosa and the right adnexa. Thyroid function was re-evaluated, and despite normal thyroid function, the TRAb test remained positive. The patient underwent total thyroidectomy and radioiodine therapy (RIT), after which the TRAb test became negative. During 3 years of follow-up, no evidence of tumor was observed. In our case of thyroid carcinoma originating in SO, hyperthyroidism was treated with ovarian surgery, total thyroidectomy, and RIT. It is worth noting that thyroid function was normalized after ovarian surgery, but the TRAb test only became negative after total thyroidectomy. We hope to draw attention to the importance of evaluating thyroid function in patients with SO and treating high-risk SO patients with RIT after total thyroidectomy to achieve disease remission.
Struma ovarii can cause hyperthyroidism. Thyroid carcinoma can originate in Struma Ovarii. Differentiated thyroid carcinoma and hyperthyroidism originating in Struma Ovarii are rare conditions.
卵巢甲状腺肿(SO)起源的甲状腺癌是一种罕见的甲状腺异位癌,占所有卵巢恶性肿瘤的0.01%,不到15%的病例伴有甲状腺功能亢进。在一名44岁有盆腔疼痛的患者中,CT扫描显示卵巢有一个实性囊性结构。实施了左侧卵巢切除术,结果显示为交界性浆液性肿瘤和一个直径10厘米的乳头状甲状腺癌(“卵巢甲状腺肿起源的甲状腺癌”)。评估了甲状腺功能,诊断为甲状腺功能亢进。进行了手术补充和盆腔再次探查。组织学检查结果显示子宫浆膜层和右侧附件有乳头状甲状腺癌。再次评估甲状腺功能,尽管甲状腺功能正常,但促甲状腺素受体抗体(TRAb)检测仍为阳性。患者接受了甲状腺全切除术和放射性碘治疗(RIT),之后TRAb检测变为阴性。在3年的随访期间,未观察到肿瘤迹象。在我们这个卵巢甲状腺肿起源甲状腺癌的病例中,甲状腺功能亢进通过卵巢手术、甲状腺全切除术和RIT进行治疗。值得注意的是,卵巢手术后甲状腺功能恢复正常,但TRAb检测仅在甲状腺全切除术后变为阴性。我们希望引起人们对评估卵巢甲状腺肿患者甲状腺功能以及对高危卵巢甲状腺肿患者在甲状腺全切除术后进行RIT治疗以实现疾病缓解的重要性的关注。
卵巢甲状腺肿可导致甲状腺功能亢进。甲状腺癌可起源于卵巢甲状腺肿。起源于卵巢甲状腺肿的分化型甲状腺癌和甲状腺功能亢进是罕见情况。