Journal of Basic and Clinical Reproductive Sciences

Journal of Basic and Clinical Reproductive Sciences
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Abhijeet Ingle*, Vijaya Gattu, Suhela Rachakonda and Sachin Subhash Marda
 
Yashoda Hospital, Hyderabad, TS, India, Email: abhiingle@yahoo.co.in
 
*Correspondence: Abhijeet Ingle, Department of Consultant Histopathologist, Yashoda Hospital, Hyderabad, India, Email: abhiingle@yahoo.co.in

Received: 30-May-2017 Accepted Date: Mar 16, 2018 ; Published: 20-Mar-2018

Citation: Ingle A, Gattu V, Rachakonda S, Marda SS A Rare Case of Peritoneal Spread of Benign Struma Ovarii with Thyrotoxicosis doi: 10.4103/2278-960X.194513

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Abstract

Background: Struma ovarii is a highly specialized form of mature ovarian teratoma consisting of thyroid tissue and exhibiting all the histological features of the thyroid gland. Malignant transformation of thyroid tissue in struma ovarii and metastasis are extremely uncommon. In rare cases, benign thyroid tissue may spread to the peritoneal cavity, and pathologic examination of the peritoneal implants shows multiple nodules of varying sizes of mature thyroid tissue similar to struma ovarii.

Summary: We report a 30-year-old woman with struma ovarii complicated by peritoneal dissemination with thyrotoxicosis. After surgical resection of the struma ovarii and peritoneal implants the patient became euthyroid.

 

Keywords

Struma ovarii; Highly differentiated follicular carcinoma of ovarian origin; Peritoneal dissemination; Radioiodine ablation; Extra-ovarian tumour.

Introduction

Twenty percent of ovarian tumours are teratomas, and up to 20% of teratomas contain thyroid tissue. Struma ovarii consisting of at least 50% of thyroid tissue [1] is less common and accounts for 1-4% of benign ovarian teratomas. Bilateral struma ovarii is very rare and has not been reported frequently [2]. Struma ovarii usually shows up as a pelvic mass and presents as pseudo-Meigs' syndrome in about 5% of cases [3]. However, preoperative diagnosis of struma ovarii is rarely reported and may occur in patients with symptoms of hyperthyroidism but this association is observed in less than 5% of cases [4].

Malignant transformation of thyroid tissue in struma ovarii and metastasis is uncommon. Benign thyroid tissue may spread to the peritoneal cavity in rare cases, and pathologic examination of the peritoneal implants shows multiple nodules of varying sizes of mature thyroid tissue similar to struma ovarii [5]. Because of its harmless histological appearance, this form of follicular carcinoma cannot be diagnosed until the neoplasm spreads beyond the ovary thus showing evidence of aggressive behaviour [6]. The differential diagnosis of peritoneal dissemination of struma includes typical thyroid carcinoma metastatic to the ovary, which has also been reported [7].

Histological features of thyroid carcinoma are found in ~ 5% struma ovarii (referred to as malignant struma ovarii) [2] The nuclear features of papillary carcinoma are usually used as the criteria for diagnosis of malignant struma ovarii, and most cases reported are papillary carcinoma [8,9]. In recent large studies on malignant struma ovarii, the clinical behaviour was difficult to predict based on tumor histomorphology alone [10]. Immunohistochemical staining with HBME-1 (Hector Battifora mesothelial [cell]-1) and galectin-3, often expressed in papillary thyroid carcinoma, can also help to confirm the diagnosis [11].

Case Report

Here we report a 30-year-old female patient G0 P2 L2A0 who was evaluated at an outside institution for left ovarian mass. Then she underwent laparoscopic left oophorectomy, and diagnosed as proliferative struma ovarii with nuclear atypia, 2 years back. The histological report was available and reviewed. Then she developed lower abdominal pain (right side) since 4-5 months, associated with weight loss.

Chest X-ray was normal and ultrasound abdomen showed multiple space occupying lesions (SOLs) in pelvis and lower abdomen bilaterally-suggestive of metastatic nodes and ascites. Thyroid profile showed raised T3, T4 and low TSH

PET CT scan of the abdomen and pelvis demonstrated multiple peritoneal deposits scattered in entire abdominal cavity with a max standardized uptake valueof 6.7 (Figures 1 and 2).

clinical-reproductive-peritoneal-deposits

Figure 1: PET CT scan of the abdomen demonstrated multiple peritoneal deposits scattered in entire abdominal cavity with a max standardized uptake value of 6.7.

clinical-reproductive-entire-abdominal

Figure 2: PET CT scan of the pelvis demonstrated multiple peritoneal deposits scattered in entire abdominal cavity with a max standardized uptake value of 6.7.

Ultrasound guided biopsy from one of the peritoneal lesions and ascitic fluid cytology revealed atypical cells.Then she underwent radical hysterectomy with right salpingo-oophorectomy, Total omentoctomy, Distal small bowel tumour resection and end to end Anastomosis, resection of anterior wall deposit, Extensive total peritonectomy, excision of mesenteric and small bowel deposit and total thyroidectomy. The specimens were submitted for histopathological examination.

Multiple grey white to brownish nodules were seen scattered all over the surface of uterus, right ovary and fallopian tube, largest nodule measuring 1.5 × 1 × 1.5 cms. (Figure 3). Omentum showed multiple grey white to brownish nodules, largest nodule measuring 3.0 × 2.5 × 2.5 cms. (Figure 4). Similar deposits were observed on small bowel, anterior abdominal wall, Pouch of Douglas (POD), paracolic gutter, and diaphragmatic peritoneum (Figures 5 and 6). Grossly thyroidectomy specimen was unremarkable.

clinical-reproductive-grey-white

Figure 3: Multiple grey white to brownish nodules were seen scattered all over the surface of uterus, right ovary and fallopian tube, largest nodule measuring 1.5 × 1 × 1.5 cm.

clinical-reproductive-brownish-nodules

Figure 4: Omentum showed multiple grey white to brownish nodules, largest nodule measuring 3.0 × 2.5 × 2.5 cms.

clinical-reproductive-small-bowel

Figure 5: Deposits were observed on small bowel, anterior abdominal wall.

clinical-reproductive-paracolic-gutter

Figure 6: Deposits were observed on pouch of douglas (POD), paracolic gutter, and diaphragmatic peritoneum.

Histopathological examination from the slides reviewed from left ovarian mass showed cyst wall lined by skin and skin adnexal structures, keratinous material and calcific debris. Also showed closely packed thyroid follicles containing thin colloid, the lining cells show mild nucleomegaly, focal nuclear overlapping, and nuclear clearing at most places. Occasional intranuclear grooves are seen; hence, diagnosed as proliferative struma ovarii with nuclear atypia (Figure 7).

clinical-reproductive-nuclear-atypia

Figure 7: Intranuclear grooves are seen as proliferative struma ovarii with nuclear atypia.

Histopathological examination from the slides reviewed from left ovarian mass showed cyst wall lined by skin and skin adnexal structures, keratinous material and calcific debris.

Histopathological examination from representative areas from above mentioned organs revealed encapsulated nodular tumours composed of closely packed micro follicles, lined by cuboidal cells having round to slightly irregular nuclei, mild anisonucleosis seen. Focally chromatin clearing and occasional intranuclear grooves seen.

The unequivocal features of papillary carcinoma were not seen. Diagnosis of peritoneal spread of benign struma ovarii was made (Metastatic highly differentiated thyroid carcinoma) (Figures 8 and 9). However sections from urinary bladder and thyroidectomy specimen were unremarkable.

clinical-reproductive-thyroid-carcinoma

Figure 8: Metastatic highly differentiated thyroid carcinoma.

clinical-reproductive-thyroid-carcinoma

Figure 9: Diagnosis of peritoneal spread of benign struma ovarii.

Immunohistochemistry performed on multiple nodules -CK19 was focally positive and p53 was negative.

Discussion

Roth et al. described in detail the cases of peritoneal implantation or dissemination of thyroid tissues.

They also proposed considering highly differentiated follicular carcinoma of ovarian origin as a new entity, which resembles thyroid goiter but causes metastasis.

In this context, some cases in which peritoneal dissemination was found at the time of surgery for ovarian tumor seems to be malignant struma ovarii, and the term ‘peritoneal strumosis’ should be used only in cases in which the primary ovarian tumor is purely benign [6].

Our patient presented with recurrence and peritoneal spread of a benign struma ovarii 2 years after the first diagnosis.

A review of 39 patients with malignant struma ovarii showed only 9 patients (23%) with metastasis.

The predominant sites were adjacent pelvic structures including the contralateral ovary, but some patients had distant metastases to the lungs, bone, liver, and brain [12].

McGill et al. performed a review on 40 patients with struma ovarii and concluded also that the recommended treatment of metastatic struma ovarii should contain total thyroidectomy in conjunction with radioiodine scanning and radioiodine ablation [13]; another two case reports came to similar conclusions [14,15].

Follow up may include the use of thyroglobulin as a tumour marker, and diagnostic radioiodine scans may be performed to screen for residual or recurrent disease [16]. Repeat ablative radioiodine treatment may still have a curative potential or at least can provide extended disease free survival. Recombinant human TSH (rhTSH) is occasionally used before 131I administration to achieve a concentration of 131I activity in the tumour high enough for a significant cytotoxic effect, because 131I uptake by most of thyroid carcinomas is quite low in absence of high levels of endogenous TSH [17,18]. Zekri et al. had described a patient with struma ovarii that was initially diagnosed as benign and presented 10 years later with distant metastases [19].

Conclusion

In our case the diagnosis at the time of first laparoscopic surgery (left oophorectomy) was benign struma ovarii with nuclear atypia. There was no evidence of malignancy in all the slides reviewed. Final diagnosis at the time of second surgery from peritoneal implants also showed benign thyroid tissue with occasional nuclear grooves. Unequivocal features of papillary thyroid carcinoma were not seen. Hence we consider our case as a ‘pure’ peritoneal strumosis.

Patient with benign metastatic struma ovarii (also known as highly differentiated follicular carcinoma of ovarian origin - HDFCO) may affectively be treated with local resection of the extra ovarian tumour and subsequent thyroidectomy followed by radioactive iodine ablation.

If preservation of fertility is desired and the carcinoma is limited to the ovary, unilateral salpingo-oophorectomy or strumectomy is suggested; otherwise, total abdominal hysterectomy and bilateral salpingo-oophorectomy are typically performed. Sequential thyroglobulin measurements along with total-body scintiscanning with I131 follow-up are recommended if recurrence is suspected. Thyroid-type carcinomas arising in struma ovarii, especially the newly recognized entity-HDFCOhave a favourable prognosis.

If preservation of fertility is desired and the carcinoma is limited to the ovary, unilateral salpingo-oophorectomy or strumectomy is suggested; otherwise, total abdominal hysterectomy and bilateral salpingo-oophorectomy are typically performed. Sequential thyroglobulin measurements along with total-body scintiscanning with I131 follow-up are recommended if recurrence is suspected. Thyroid-type carcinomas arising in struma ovarii, especially the newly recognized entity-HDFCOhave a favourable prognosis.

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