- Author:
Sang Mi KIM
1
;
Bo Kwang CHOI
;
Ji Hyun KANG
;
Mi Ra KIM
;
Yun Kyung JEON
;
Sang Soo KIM
;
Bo Hyun KIM
;
In Ju KIM
Author Information
- Publication Type:Case Report
- Keywords: Bilateral struma ovarii; Hyperthyroidism; Ovarian neoplasms
- MeSH: Abdominal Pain; Accounting; Goiter; Humans; Hyperthyroidism; Incidence; Ovarian Neoplasms; Struma Ovarii; Teratoma; Thyroid Gland; Thyrotoxicosis
- From:Endocrinology and Metabolism 2012;27(1):72-76
- CountryRepublic of Korea
- Language:Korean
- Abstract: Struma ovarii is a rare monodermal variant of ovarian teratoma accounting for only 2% of all mature teratomas. To be classified as a struma ovarii, teratoma must be composed predominantly of mature thyroid tissue (> 50%). This tumor is generally benign, although malignant transformation has been reported. Struma ovarii occur mostly as unilateral cases, so bilateral cases are quite rare (less than 6% of cases). Struma ovarii occur largely without symptoms or are accompanied by non-specific symptoms, such as abdominal pain, a palpable abdominal mass, and abdominal distension. The preoperative diagnosis is generally difficult. The incidence of hyperthyroidism has been reported to be 5-10% of patients with struma ovarii. Thus, cases of functional bilateral struma ovarii are very rare. We report a case of bilateral struma ovarii with subclinical thyrotoxicosis and a diffuse goiter, mimicking a malignant ovarian tumor, and include a brief review of related literature.