Advanced Stage Clear Cell Ovarian Carcinoma Mimicking Uterine Sarcoma Without Gross Residual Tumor During Primary Surgery: A Case Report.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Clinical Medicine Insights. Case Reports Pub Date : 2023-01-01 DOI:10.1177/11795476231166623
Yoan Alexandria Angelina, Brahmana Askandar Tjokroprawiro
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Abstract

Background: Clear cell ovarian carcinoma is rare and accounts for 1%-12% of ovarian epithelial carcinomas, depending on ethnicity. The prevalence of clear cell ovarian carcinoma in Asian, White, and Black women is 11.1%%, 4.8%, and 3.1%, respectively. Magnetic resonance imaging (MRI) shows that clear cell ovarian carcinomas are typically unilocular cyst-solid (34.9%) or multilocular-solid (41.4%); only 23.7% are solid with papillary projections. MRI can detect clear cell ovarian carcinoma with a sensitivity and specificity of 90% and 87%, respectively. Notably, sometimes ovarian masses have a solid feature and should be differentiated from uterine masses. Clear cell ovarian carcinoma has a better prognosis compared to serous carcinoma when diagnosed at an early stage, but it has a poorer prognosis at an advanced stage. The absence of a residual tumor is a favorable prognostic factor in patients with advanced-stage clear cell ovarian carcinoma. Herein, we present a case in which clear cell ovarian carcinoma was misdiagnosed as uterine sarcoma because imaging showed a mass with a solid uterine-like and necrotic area. In the present case, cytoreductive surgery was performed to remove the entire tumor and its infiltration to the sigmoid colon and left ureter. Hence, the patient had a better prognosis.

Case report: A 57-year-old Indonesian woman presented to our hospital (Dr. Soetomo General Hospital) with post-menopausal bleeding, a large solid pelvic mass, and abdominal discomfort. The patient was diagnosed with uterine sarcoma due to the solid feature observed during ultrasonography and MRI. During the surgery, the mass was observed to originate from the left ovary, and primary debulking surgery with a multidisciplinary team was performed with zero residual tumor tissue. The tumor was histopathologically confirmed as clear cell carcinoma.

Conclusion: MRI of clear cell ovarian carcinoma can be misdiagnosed as uterine sarcoma due to its solid feature. Additionally, the enlarged mass distorts the anatomical landmarks. Surgery with no residual tumor improves the prognosis for advanced-stage clear cell ovarian carcinoma.

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晚期透明细胞卵巢癌模拟子宫肉瘤原发手术无大体残留肿瘤1例报告。
背景:透明细胞卵巢癌是罕见的,占卵巢上皮癌的1%-12%,这取决于种族。透明细胞卵巢癌在亚洲、白人和黑人女性中的患病率分别为11.1%、4.8%和3.1%。磁共振成像(MRI)显示,透明细胞卵巢癌典型表现为单房囊肿实性(34.9%)或多房实性(41.4%);仅有23.7%为实性伴乳头状突起。MRI对卵巢透明细胞癌的诊断敏感性为90%,特异性为87%。值得注意的是,卵巢肿块有时呈实性特征,应与子宫肿块鉴别。透明细胞卵巢癌在早期诊断时预后较浆液性癌好,但在晚期诊断时预后较差。无残留肿瘤是晚期透明细胞卵巢癌患者预后的有利因素。在此,我们报告一个透明细胞卵巢癌被误诊为子宫肉瘤的病例,因为影像显示一个有实质子宫样坏死区域的肿块。在本病例中,我们进行了细胞减少手术,切除了整个肿瘤及其浸润到乙状结肠和左输尿管。因此,患者预后较好。病例报告:一名57岁印度尼西亚妇女因绝经后出血、大实心盆腔肿块及腹部不适来到我院(Soetomo综合医院)。经超声及MRI检查发现子宫肉瘤呈实性征,诊断为子宫肉瘤。在手术中,肿块被观察到起源于左卵巢,并与多学科团队进行了原发性减体积手术,肿瘤组织零残留。组织病理学证实为透明细胞癌。结论:透明细胞卵巢癌的MRI表现为实性,易误诊为子宫肉瘤。此外,扩大的肿块扭曲解剖标志。无残留肿瘤的手术可改善晚期透明细胞卵巢癌的预后。
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来源期刊
Clinical Medicine Insights. Case Reports
Clinical Medicine Insights. Case Reports MEDICINE, GENERAL & INTERNAL-
CiteScore
1.10
自引率
0.00%
发文量
57
审稿时长
8 weeks
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