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CASE REPORT
Year : 2021  |  Volume : 5  |  Issue : 2  |  Page : 85-87

Proliferative struma ovarii: A rare case report


1 Department of Pathology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh, India
2 Department of Obstetrics and Gynaecology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh, India

Correspondence Address:
Gagan Kumar Rangari
Department of Pathology, Institute of Medical Sciences, Banaras Hindu University, Semicircle Road Number 4, Varanasi - 221 005, Uttar Pradesh
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijcpc.ijcpc_9_21

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Dermoid cyst is the most common ovarian neoplasm, comprising up to 25% or more of all ovarian tumors, and contains various mature tissues derived from one or more of the embryonic germ layers, the ectoderm, mesoderm, and endoderm but occasionally transform to malignant. Struma ovarii is defined as teratoma containing predominantly thyroid tissue up to 50% of the cases. Stroma ovarii is a very unusual and rare type of teratoma and has been demonstrated in 5%–20% of the cases and comprises 3% of ovarian teratomas. For struma ovarii, patient age ranges between 6 and 74 years and most patients are in their reproductive years. Struma ovarii is predominantly unilateral and associated with mature cystic teratoma, ascites, pleural effusion, and rarely with a cystadenoma. Tumor is composed of mature thyroid tissue comprising varying sizes of follicles lined by columnar or flattened epithelium. Sometimes, the follicles are markedly crowded, but other criteria of malignancy are absent, and hence, these cases are reported as proliferative struma ovarii. Proliferative struma ovarii has a good prognosis. Some benign cases are misdiagnosed as carcinoma when serum CA-125 is highly raised. As there are no specific clinical, radiological, and serological markers available for this rare tumor, these are diagnosed on histopathology.


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