Abstract

<i>Background</i>: Ovarian steroid cell tumors are rare tumors of the ovary characterized by steroid cell proliferation. These sex-hormone secreting tumors raise many differential diagnoses related to hyperandrogenism. Although most of these tumors are benign and slow-growing, approximately 25 – 43% of cases are clinically malignant. <i>Case</i>: We herein report a case of 30 years old woman with ovarian steroid cell tumor, not otherwise specified (NOS) with primary infertility. The patient presented with hirsutism and abdominal enlargement due to massive ascites during hospital admission. The blood test result showed significantly increased CA-125. Transabdominal ultrasound revealed a 7.81 x 4.94 cm tumor of the left adnexa. The patient underwent left salpingo-oophorectomy and responded well to the surgery. <i>Conclusion</i>: This case report presents a unique case of ovarian steroid cell tumor, NOS with findings of massive ascites, hirsutism, and a high level of CA-125. The findings were never associated with this type of tumor. The steroid cell tumor and its ascites could mechanically irritate the mesothelium that causing overexpression of CA-125. Surgery remains as the first-line treatment of this case. Adjuvant chemotherapy should be done based on the histologic type of the tumor and its surgical stage. Tumor marker decreased after surgery was done and patient remains alive and free of disease after a period of 2 years.

Highlights

  • Ovarian steroid cell tumors are uncommon sex-hormone secreting tumors characterized by a steroid cell proliferation

  • Transabdominal ultrasound revealed an anteflexed uterus with an endometrial thickness of 0.50 cm, hypoechoic mass with a size of 7.81 x 4.94 cm which derives from the left adnexa was seen along with a solid tumor accompanied by massive ascites

  • The patient presented with hirsutism and primary infertility which are the symptoms of ovarian steroid cell tumors

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Summary

Introduction

Ovarian steroid cell tumors are uncommon sex-hormone secreting tumors characterized by a steroid cell proliferation It is a rare type of sex cord-stromal tumours of the ovary. Ovarian steroid cell tumour are classified into three subtypes: stromal luteoma, Leydig cell tumour, and steroid cell tumour not otherwise specified (NOS). This case report describes the case of a 30-year-old woman with an ovarian steroid cell tumor, NOS (not otherwise specified), of the ovary. The Patient had a complete response to surgery which was her only treatment

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