Groener Daniel, Baumgarten Justus, Happel Christian, Mader Nicolai, Ngoc Christina Nguyen, Sabet Amir, Grünwald Frank
Department of Nuclear Medicine University Hospital Frankfurt Frankfurt Germany.
Clin Case Rep. 2023 May 4;11(5):e7311. doi: 10.1002/ccr3.7311. eCollection 2023 May.
In this case of struma ovarii a right-sided ovarian mass contained features of papillary thyroid cancer. Diagnostic iodine-123 revealed multiple foci of extraovarian spread, likely as a manifestation of concomitant peritoneal strumosis. Unilateral oophorectomy, partial peritonectomy, and adjuvant iodine-131 treatment were performed for successful curative treatment.
Struma ovarii is a rare form of mature teratoma defined by a predominance of thyroid tissue. Approximately 5% of all ovarian strumae exhibit malignant transformation. Due to their extreme rarity, there has been a lack of consensus concerning uniform diagnostic criteria. Appropriate, risk-stratified treatment strategies also remain widely unelaborated, based only on a small number of cases reported in the literature. We describe the case of a 35-year-old female, who presented after undergoing unilateral oophorectomy for a right-sided ovarian mass. Histological workup revealed a struma ovarii containing papillary thyroid cancer (PTC). Postoperative I-123 scintigraphy with single photon emission computed tomography (SPECT) detected multifocal extra-ovarian spread to the peritoneum, containing likely benign strumosis upon pathological examination. The subsequent treatment strategy involved an ablative concept including total thyroidectomy and subsequent I-131 radioiodine therapy. Throughout a 3-year follow-up, the patient has remained without recurrence with thyroglobulin levels ranging below detection limits. Surgical resection with adjuvant radioiodine therapy is a curative therapeutic strategy in cases of struma ovarii with thyroid-type carcinoma and peritoneal strumosis. Its benefits lay in avoiding more extensive surgery, potentially maintaining fertility, facilitating follow-up, and minimizing the risk of recurrence. Reliable criteria for risk stratification are needed to identify patients who are most likely to benefit from this treatment approach.
在这例卵巢甲状腺肿病例中,右侧卵巢肿物具有乳头状甲状腺癌的特征。诊断性碘-123检查显示存在多处卵巢外扩散灶,可能是并发腹膜甲状腺肿的表现。行单侧卵巢切除术、部分腹膜切除术及辅助碘-131治疗,成功实现了根治性治疗。
卵巢甲状腺肿是一种罕见的成熟畸胎瘤,其特征是以甲状腺组织为主。所有卵巢甲状腺肿中约5%会发生恶变。由于其极为罕见,对于统一的诊断标准尚无共识。基于文献中仅报道的少数病例,合适的、风险分层的治疗策略也仍未得到充分阐述。我们描述了一名35岁女性的病例,她因右侧卵巢肿物接受单侧卵巢切除术后前来就诊。组织学检查显示为含有乳头状甲状腺癌(PTC)的卵巢甲状腺肿。术后碘-123单光子发射计算机断层扫描(SPECT)闪烁显像检测到多灶性卵巢外扩散至腹膜,病理检查显示可能为良性甲状腺肿。后续的治疗策略包括根治性方案,即全甲状腺切除术及随后的碘-131放射性碘治疗。在3年的随访中,患者未复发,甲状腺球蛋白水平低于检测限。对于伴有甲状腺型癌和腹膜甲状腺肿的卵巢甲状腺肿病例,手术切除并辅助放射性碘治疗是一种根治性治疗策略。其益处在于避免更广泛的手术、可能维持生育能力、便于随访并将复发风险降至最低。需要可靠的风险分层标准来识别最可能从这种治疗方法中获益的患者。