Skip Navigation Links.
Collapse <span class="m110 colortj mt20 fontw700">Volume 12 (2024)</span>Volume 12 (2024)
Collapse <span class="m110 colortj mt20 fontw700">Volume 11 (2023)</span>Volume 11 (2023)
Collapse <span class="m110 colortj mt20 fontw700">Volume 10 (2022)</span>Volume 10 (2022)
Collapse <span class="m110 colortj mt20 fontw700">Volume 9 (2021)</span>Volume 9 (2021)
Collapse <span class="m110 colortj mt20 fontw700">Volume 8 (2020)</span>Volume 8 (2020)
Collapse <span class="m110 colortj mt20 fontw700">Volume 7 (2019)</span>Volume 7 (2019)
Collapse <span class="m110 colortj mt20 fontw700">Volume 6 (2018)</span>Volume 6 (2018)
Collapse <span class="m110 colortj mt20 fontw700">Volume 5 (2017)</span>Volume 5 (2017)
Collapse <span class="m110 colortj mt20 fontw700">Volume 4 (2016)</span>Volume 4 (2016)
Collapse <span class="m110 colortj mt20 fontw700">Volume 3 (2015)</span>Volume 3 (2015)
Collapse <span class="m110 colortj mt20 fontw700">Volume 2 (2014)</span>Volume 2 (2014)
Collapse <span class="m110 colortj mt20 fontw700">Volume 1 (2013)</span>Volume 1 (2013)
American Journal of Public Health Research. 2015, 3(5A), 144-147
DOI: 10.12691/AJPHR-3-5A-31
Research Article

Clinical and Histopathological Study of Struma Ovarii: A Rare Ovarian Tumor

Dilasma Ghartimagar1, , Arnab Ghosh1, Manish Kiran Shrestha2, Sushma Thapa1, Tilottama Prasad1, Raghavan Narasimhan1 and O P Talwar1

1Department of Pathology, Manipal College of Medical Sciences, Pokhara, Nepal

2Department of Radiology, Gandaki Medical College, Pokhara, Nepal

Pub. Date: October 28, 2015
(This article belongs to the Special Issue Health Scenario 2015; Millennium Development Goals)

Cite this paper

Dilasma Ghartimagar, Arnab Ghosh, Manish Kiran Shrestha, Sushma Thapa, Tilottama Prasad, Raghavan Narasimhan and O P Talwar. Clinical and Histopathological Study of Struma Ovarii: A Rare Ovarian Tumor. American Journal of Public Health Research. 2015; 3(5A):144-147. doi: 10.12691/AJPHR-3-5A-31

Abstract

Struma ovarii or monodermal teratoma is a specialized ovarian neoplasm which mainly constitutes mature thyroid tissue. It is a rare tumor which comprises 1% of all ovarian tumors and 2.7% of all dermoid tumors. Thyroid tissue can be observed in 5-15% of dermoid tumors but to designate the tumor as struma ovarii, it must comprise more than 50% of the ovarian tissue. This study was conducted in the Department of Pathology, Manipal Teaching Hospital in Pokhara, Nepal over a period of 10 years (Jan 2006 to Sep 2015). Age, clinical findings, pre-operative imaging diagnosis, size and side of the tumor, gross and microscopic findings along with type of surgery performed are included in the study. During this 10 years period, there were 7 cases of struma ovarii with age ranging from 26 to 56 years. 3 cases had tumor on the right and 3 cases had tumor on the left side while 1 case had bilateral struma ovarii. Initial presenting symptom was palpable mass, abdominal pain and vaginal bleeding. The size of the tumor ranged from 4 to 15 cm. The capsule was smooth and cut surface shows multiloculated cyst filled with greenish to pale brown gelatinous thick fluid. Microscopic examination revealed well encapsulated tumor composed entirely of thyroid follicles. Diagnoses of struma ovarii were made in all cases. The preoperative imaging may not exactly give the diagnosis. Clinically, lesser age group was more affected and left side is more commonly involved in our series, in contrary to other literature. Out of 7 cases, bilateral struma ovarii was seen in 1 patient. No malignant features were seen in any of these cases.

Keywords

monodermal teratoma, ovarian tumor, struma ovarii

Copyright

Creative CommonsThis work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

References

[1]  SinghalS, SinghS, SinghalS. Struma Ovarii - A Rare Ovarian Tumor. The Internet Journal of Gynecology and Obstetrics. 2008 Volume 12 Number 1.
 
[2]  Ellinson LR, Pirog EC. The female genital tract. In Kumar, Abbas, Fausto, Aster, editors. Robbins and Cotran PathologicBasis of Disease. 8th ed. Philadelphia, Pennsylvania: Elsevier; 2011. p. 1048.
 
[3]  Talerman A, Roth LM. Recent advances in the pathology and classification of gonadal neoplasms composed of germcells and sex cord derivatives. Int J Gynecol Pathol 2007; 26: 313-21.
 
[4]  Kim SJ, Pak K, Lim HJ, Yun KH, Seong SJ, Kim TJ, et al. Clinical diversity of struma ovarii. Korean J Obstet Gynecol 2002; 45: 748-52.
 
[5]  Raina A, Stasis G, Monzio Compagnoni, B et al. Struma Ovarii :A rare gynecological tumour. Acta Oncol.1997;36:533-4.
 
[6]  Yannopoulos D, Yannopoulos K, Ossowaski R. Malignant struma ovarii. Pathol Ann. 1976; 11: 403-13.
 
[7]  Boettlin R. Uber zahnentwickelung in dermoid cysten des ovariums. Virchows Arch Path Arat 1889; 115: 493-504.
 
[8]  Gottschalk S. Ein neuer typus einer kleincystischen bosartigen eierstockgeschwulst. Arch Gynak 1899; 59: 676-98.
 
[9]  Bethune M, Quinn M, Rome R. Struma ovarii presenting as acute pseudo Meigs syndrome with elevated CA 125 level, Aust N Z J Obstet Gynecol 1996; 36: 372-3.
 
[10]  Seung-Chul Yoo, Ki-Hong Chang, Mi-Ok Lyu, Suk-Joon Chang, Hee-Sug Ryu, Haeng-Soo Kim. Clinical characteristics of struma ovarii. J Gynecol Oncol June 2008; 19(2):135-8.
 
[11]  Khediri Z, Mbarki C, Abdelaziz AB, Hsayoui N, Mezghenni S, Oueslati H. Struma ovaii: clinical presentations of an uncommon tumor. IJCRI 2012; 3 (4): 10-4.
 
[12]  Kaur S, Bodal VK, Bal MS, Bhagat R, Gupta N,Ohari D. Hyperthyroidism with Struma ovarii. Int J Med and Dent Sci 2014; 3(1):344-7.
 
[13]  Bhansali A, Jain V, Rajwanshi A, Lodha S, Dash RJ. Follicular carcinoma in a functioning struma ovarii. Postgrad Med J 1999; 75: 617-8.
 
[14]  Zalel Y, Seidman DS, Oren M, Achiron R, Gotlieb W, Mashiach S, et al. Sonographic and clinical characteristics of struma ovarii. Ultrasound Med 2000; 19: 857-61.
 
[15]  Robboy SJ, Shaco-Levy R, Peng RY, Snyder MJ, Donahue J, Bentley RC et al. Malignant Struma Ovarii: An Analysis of 88 Cases, Including 27 With Extraovarian Spread. Int J Gynecol Pathol. 2009; 28(5): 405-22.
 
[16]  Ayhan A, Yanik F, Tuncer R, Tuncer ZS, Ruacan S. Struma ovarii. Int J Gynaecol Obstet 1993; 42: 143-6.
 
[17]  Marcus CC, Marcus SL. Struma ovarii. A report of 7 cases and a review of the subject. Am J Obstet Gynecol 1961; 81: 752-62.
 
[18]  Dohke M, Watanabe Y, Takahashi A, Katayama T, Amoh Y, Ishimori T, et al. Struma ovarii: MR findings. J Comput Assit Tomogr 1997;21: 256-7.
 
[19]  Nogales F, Talerman A, Kubik-Huch RA, Tavassoli FA, Devouassoux-Shisheboran M. Germ cell tumors. In: Tavassoli FA, Devilee P, editors. Pathology and genetics of tumours of the breast and female genital organs. IARC Press, Lyon; 2003.p. 163-75.
 
[20]  Szyfelbein WM, Young RH, Scully RE. Cystic struma ovarii: Frequently unrecognized tumor. Report of 20 cases. MJ Search Pathol. 1994; 18: 785-8.
 
[21]  Scully RE. Recent progress in ovarian cancer. Hum Pathol 1970; 1: 73-98.
 
[22]  Rana V, Srinivas V, Bandyopadhyay, Ghosh SK, Singh Y. Bilateral benign non functional struma ovarii with Pseudo-Meigs’ syndrome. IJPM. 2009;52(1):94-6.
 
[23]  Dardik RB, Dardik M, Westra W, Montz FJ. Malignant struma ovarii: Two case reports and a review of the literature. Gynecol Oncol 1999;73:447-51.