Struma Ovarii: Single Center Experience.

Patients aged 17 and above, who underwent surgery due to ovarian masses and were histopathologically diagnosed with SO, between January 2012 and January 2022 at Baskent University, were included in this study. Patient records were retrospectively reviewed to document demographic information, presenting complaints, radiological findings, laboratory data, surgical procedures performed, pathology reports, additional treatments administered, and follow-up information. Results were analyzed through a review of the literature. This study was approved by the Baskent University Non-interventional Clinical Research Ethics Committee (Number: 23/110, Date: 21.06.2023), was designed in accordance with the principles of the Declaration of Helsinki, and was supported by the Baskent University Research Fund with project number KA23/215.

Nineteen patients with a histopathological diagnosis of SO were included in the study. The average age of the patients was 41.7 (17-74) years. The most common presenting complaint among the patients was abdominal pain. The majority of patients had tumor diameters between 5-10 cm (52.6%). Laboratory data indicated that thyroid stimulating hormone (TSH) results were within normal limits, while CA 125 levels were elevated in 3 patients (15.7%). In the treatment of benign cases, tumor enucleation was the preferred approach in the majority (52.6%) of cases. There were no patients with a preoperative diagnosis of struma ovarii. All diagnoses were made by histopathological examination. Three patients (15.7%) were diagnosed with malign struma ovarii (MSO). Since these patients were between the ages of 31 and 41, unilateral salpingo-oophorectomy (USO) was chosen to preserve fertility. Papillary carcinoma was detected in two patients, and mixed papillary and anaplastic carcinoma was detected in one patient. During the follow-up of the patient, who had mixed papillary and anaplastic cancer components, metastatic lesions were observed in the vertebra in the 3 rd year and in the opposite adnexal region in the 4 th year. Surgery following vertebral-directed radiotherapy included hysterectomy, contralateral salpingo-oophorectomy, omentectomy, and pelvic lymph node dissection (PLND) in the adnexal region as additional components of treatment. Patients diagnosed with MSO received treatment consisting of total thyroidectomy, radioactive iodine ablation (RAI), and TSH suppression using L-thyroxine. The follow-up period of the patients varied between 14-112 months. The average follow-up period was 56 months. There was no recurrence or mortality recorded during the follow-up period ( Table 1 ). Demographic data of patients AP: Abdominal pain; B: Benign; I: Incidental; M: Malignant; MI: Menstureal irregularity; N: Normal; PM: Palpable mass; P: Papillary cancer; PA: Papillary + anaplastic cancer.

This study presents a large number of cases, including 19 patients diagnosed with struma ovarii in the last decade and treated in a single center. Despite being an ovarian tumor, the treatment of SO requires a multidisciplinary approach involving gynecology, endocrinology, endocrine surgery, nuclear medicine, and medical oncology clinics, given its inclusion of thyroid tissue. Differences in treatment approaches, especially in cases of malignant struma ovarii, increase interest in the subject. In the literature review by Leustean et al. [ 9 ] in 2021, less than 200 cases of struma ovarii were found. Therefore, the results of our study may contribute significantly to the development of follow-up and treatment guidelines. Furthermore, our study has shed light on the variability in the disease course of MSO, depending on the tumor components, which is another important finding. SO is most commonly observed in individuals between the ages of 31 and 50, and the peak incidence occurs in women aged 40 and above; however, there have also been reported cases in the pediatric age group. Many cases of SO are asymptomatic. Various studies have indicated that the most frequently reported symptoms include lower abdominal pain, the presence of an abdominal mass, and vaginal bleeding. [ 10 , 11 ] Although the average age in our cases was 41.7 (17-74) years, we had 4 patients under the age of 30 and our youngest patient was 17 years old. The high size of the lesions in these patients also suggested the possibility of late diagnosis. The most common complaint was abdominal pain, consistent with the literature. The characteristic feature of SO on ultrasonography, which is considered the most effective radiological method for detecting ovarian masses, is the presence of a smooth-edged, solid tissue mass often referred to as a "struma pearl," with vascularity on Doppler imaging. [ 12 ] Furthermore, SO appears as a multiloculated cystic mass on diffusion-weighted Magnetic Resonance Imaging (MRI). Nevertheless, the radiological diagnosis often remains unclear. In our study, we did not observe any patients with radiologically specific findings that conclusively confirmed the diagnosis. None of the patients displayed the typical "struma pearl" appearance on ultrasonography. According to the literature, SO masses can vary in size, ranging from 4 to 25 cm. It is worth noting that masses larger than 4 cm have a higher potential for malignancy. [ 8 , 11 ] In our patient group, all but two had a mass size exceeding 5 cm. In malignant patients, the size was over 5 cm in all patients and the average size was 9.3 cm (5 to 13 cm). It was compatible with the literature. Cancer antigen 125 (CA125) is a high molecular weight mucinous glycoprotein overexpressed on the membrane of epithelial ovarian cancer (EOC) cells. It has clinical relevance as a standard-of-care serum biomarker for ovarian cancer surveillance despite expression in some non-gynecologic malignancies and benign conditions such as pregnancy, menstruation, endometriosis, liver disease, and congestive heart failure. Post-treatment elevation of serum CA125 level in EOC patients serves as an indicator of progressive disease and finds clinical application in the management of patients with documented evidence of ovarian cancer. [ 13 ] Patients diagnosed with SO do not have a specific tumor marker. Limited studies have shown elevated CA125 levels in some cases. [ 14 ] There is ongoing debate regarding the cause of elevated CA125 levels in SO patients. Although rare, cases of SO with Pseudo-Meigs’ syndrome findings (ovarian mass, ascites, pleural effusion) and elevated CA125 have been reported. [ 15 - 20 ] These are cases reported in the literature as a limited number of case reports. ( Table 2 ). It is believed that CA125 expression originates more from mesothelial cells rather than the tumor itself. Both tumor-related and ascitic fluid-induced inflammatory responses increase CA125 expression from mesothelial cells. Despite this effect of ascites on serum CA125 level, a parallel relationship has not been clearly demonstrated. [ 21 ] In our study, CA125 levels were high in only 3 of 19 patients (15.7%), and these levels were lower than other examples in the literature. While one of these patients was pregnant, the other two patients had moderate ascites in the abdomen along with an ovarian mass. The increase in CA125 may be attributed to the inflammatory process caused by ascites in these cases. Struma ovarii associated with Pseudo-Meigs' syndrome and elevated CA125 level: reported cases TAH: Total abdominal hysterectomy; BSO: Bilateral salpingophorectomy. Although there is no pathology in the thyroid gland, high Tg suggests ectopic Tg production. According to recent literature, the only ovarian neoplasm that secretes Tg is the SO. Tg levels are especially important in monitoring recurrence. [ 22 ] In our study, the only patient with high Tg levels during follow-up was the patient diagnosed by MSO with mixed anaplastic and papillary cancer. In this patient, Tg increased to 5000 µg/L by the occurrence of metastatic lesions in the vertebra and opposite adnexa. After surgery for these metastases, thyroglobulin levels decreased to normal values ( Fig. 1 ). Thyroglobulin course in metastatic case. The most common type of carcinoma that develops in the background of struma ovarii is papillary thyroid carcinoma, which accounts for approximately 40-50% of cases. Following that, follicular thyroid carcinoma, mixed follicular and papillary thyroid carcinoma, and rarely, anaplastic and medullary carcinoma can be observed. [ 23 ] In our study, the histopathological diagnosis of 16 patients was benign. Approximately 5-10% of SO cases have malignant features. [ 9 ] Our malign struma ovarii rate was above normal at 15.7%. Two of the malignant cases had histopathology consistent with papillary thyroid carcinoma, while the third case had a mixed papillary and anaplastic carcinoma ( Figs. 2 , 3 ). Microphotographs reveals a malignant struma ovarii. Poorly differentiated papillary carcinoma of thyroid (PTC) adjacent to luteinized cells (*) in ovary (A, HEx40). Tumor contains well differentiated areas with papillary structures (B, HE x100) and anaplastic carcinoma transformation represented with bizaar nuclei with (C, HE x200) and tumor necrosis (D, HE x40). Benign thyroid tissue close to epitejial cyst in an ovarian monodermal teratoma (HE X40). In the treatment of benign cases, tumor enucleation or unilateral oophorectomy is often sufficient. However, for malignant cases, there is still no consensus on the optimal approach. Literature data primarily consist of case reports rather than large cohort studies. In addition to considering the menopausal status of patients, the differentiation between benign and malignant lesions through frozen section examination is crucial in making surgical decisions. If the frozen section sampling result indicates a benign lesion, conservative treatment can be pursued. In case of malignancy, fertility-sparing salpingo-oophorectomy or tumor enucleation can be performed in premenopausal patients, while total abdominal hysterectomy and bilateral salpingo-oophorectomy are recommended in postmenopausal patients. [ 24 ] In our series, surgical decisions were based on the frozen section sampling results and the menopausal status of the patients. Laparoscopic tumor enucleation was predominantly performed for benign cases, whereas salpingo-oophorectomy was preferred for malignant cases ( Table 3 ). Types of surgery TAH: Total abdominal hysterectomy; USO: Unilateral salpingophorectomy; BSO: Bilateral salpingophorectomy; PLND: Pelvic Lymph node dissection. There is also controversy regarding adjuvant therapy in MSO patients, similar to the uncertainty in surgical treatment. The recommended adjuvant treatment to prevent recurrence and metastasis in MSO cases is RAI treatment with total thyroidectomy. [ 8 , 23 , 25 ] This approach helps exclude thyroid cancer with thyroidectomy, allows for RAI for potential micrometastases, and enhances the reliability of Tg for follow-up. [ 26 ] Synchronous thyroid cancer is rare in MSO patients. Sisti et al. [ 27 ] reported two cases of thyroid malignancies in 21 MSO patients, one synchronous and one metachronous, while Goffredo et al. [ 28 ] mentioned six cases of thyroid cancer coexistence in 68 MSO patients. While the reasons for such coexistence are not fully understood, it is presumed that the probability of representing a synchronous tumor is higher than metastasis. Therefore, clinical examination and ultrasound evaluation of the thyroid gland should be performed in these patients. Although elevated Tg and TSH levels have been previously considered as high-risk indicators for the presence of synchronous thyroid carcinoma, numerous studies have yielded different results. [ 2 , 29 , 30 ] Euthyroid and subclinical hyperthyroid patients have been reported ( Table 4 ). While it is recommended to perform thyroidectomy followed by RAI ablation for the reliability of Tg as a marker in the monitoring of metastasis and recurrence, this issue remains controversial. Li et al. [ 31 ] concluded that RAI treatment, while reducing the recurrence in non-metastatic cases, does not contribute to overall survival and may not be mandatory. In the same study, they showed that MSO is a cancer type with a low risk of death, similar to thyroid cancer. They also noted that the prognosis is influenced by patient age, the presence of metastatic disease, and tumor type. Hinshaw et al. [ 32 ] have also proposed guidelines for postoperative management of the thyroid. They suggested that for low-risk tumors, defined as those smaller than 2 cm and with low differentiation, TSH suppression and Tg measurements may be sufficient, but they did not specify criteria for the high-risk group. In our study, since all malignant patients had tumor sizes exceeding 5 cm, total thyroidectomy, followed by RAI ablation and L-thyroxine suppression, was performed as additional treatment regardless of tumor type. No malignancies were found in the thyroid pathology of these patients. Simultaneous thyroid cancer and Tg-TSH levels N: Normal; SHT: Subclinic hyperthyroid. In the literature, post-treatment metastasis has been reported at a rate of 5-23%, and recurrence at a rate of 7.5-35%. [ 9 ] There was no recurrence in any patient in our study. Metastasis was observed during the follow-up of the patient with mixed anaplastic and papillary carcinoma among the patients diagnosed with MSO. The histopathology of the metastatic lesions revealed poorly differentiated thyroid carcinoma. The follow-up period of all patients was long enough. The last surgery for the lesion in the vertebra was performed in the metastatic patient 6 months ago, and disease-free follow-up continued in all patients, including this patient. There were no mortalities during the follow-up period. It is evident that the tumor type plays a significant role in the disease progression. Our study had limitations, including its retrospective nature, the rarity of MSO and the absence of a comparison group.

Fertility-preserving conservative surgery is recommended for benign struma ovarii nonetheless, there are uncertainties regarding MSO. Factors such as the rarity of malignancy and the absence of a pre-surgery diagnosis contribute to these uncertainties. Although there are publications in the literature recommending aggressive treatment in cases of malignant struma ovarii, our study suggests that if the histopathological examination reveals no aggressive components in the tumor, fertility-sparing surgery, with an assessment of the risk, may be sufficient for treatment. However, future studies with larger series and comparison groups are necessary to elucidate treatment strategies