Female Genital Tuberculosis, a Rare Lesion Mimicking Ovarian Carcinoma, with Granulosa Cell Tumor: A Case Report

R. Samaka, A. Mohamed, A. Abu-Zeid
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Abstract

Introduction: Tuberculosis (TB) of the upper genital tract is a rare disease worldwide. TB should be always considered in the differential diagnosis of a pelvic or adnexal mass as it may diagnosed as ovarian carcinoma but both have completely different treatment. Therefore, recognition of TB is important for surgeons and histopathologists, in order to set a proper plan for management and avoid unnecessary extensive therapy. Granulosa cell tumor of the ovary is a rare type of ovarian cancer that accounts for approximately 2% of all ovarian tumors. This type of tumor is known as a sex cord-stromal tumor and usually occurs in adults. Thorough search in English literature revealed only 2 case reports showed combination between genital TB and granulosa cell tumor. Case summary: A 68 years old female patient complained of vaginal bleeding for four months. She had no personal or family history of TB. An ultrasound study showed a 2x1.5 cm mixed echogenic mass in the right adnexa. Based on her clinical and imaging findings which suggestive of ovarian cancer, the patient underwent panhystrectomy and bilateral salpingoophrectomy. The gross examination of the specimen revealed distended and coiled tubes with right adnexal mass measured 2x1.5 cm and dissection of the uterus revealed erythematous endometrium with yellowish secretions. The histopathologic assessment of right adnexal mass revealed malignant neoplasm *Granulosa cell tumor* formed of short polygonal cells arranged in diffuse sheets with patternless pattern. The malignant cells showed nuclear grooving. There was no necrosis or other ovarian neoplastic element. The histopathologic assessment of both tubes and endometrium revealed infiltration by multiple nodular granulomas. Each granuloma was formed of multinucleated giant cells and epithelioid cells rimmed by lymphocytes with occasional central caseation *genital tuberculosis*. Conclusion: The conclusion of this case report is to stress upon keeping genital TB in mind as a potential differential diagnosis for ovarian carcinoma.
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女性生殖器结核是一种罕见的类似卵巢癌的病变,并伴有颗粒细胞瘤1例
上生殖道结核(TB)在世界范围内是一种罕见的疾病。在鉴别诊断盆腔或附件肿块时应始终考虑结核病,因为它可能被诊断为卵巢癌,但两者的治疗方法完全不同。因此,对于外科医生和组织病理学家来说,认识到结核病是很重要的,以便制定适当的管理计划,避免不必要的广泛治疗。卵巢颗粒细胞瘤是一种罕见的卵巢癌类型,约占所有卵巢肿瘤的2%。这种类型的肿瘤被称为性索间质瘤,通常发生在成人身上。通过查阅英文文献发现,仅有2例报告显示生殖器结核与颗粒细胞瘤合并。病例总结:一名68岁女性患者,主诉阴道出血4个月。她没有个人或家族结核病病史。超声检查显示右附件2 × 1.5 cm混合性回声肿块。由于临床和影像学表现提示卵巢癌,患者接受了全子宫切除术和双侧输卵管切除术。肉眼检查显示右侧附件肿块2 × 1.5 cm,肿胀卷曲的输卵管,子宫剥离显示子宫内膜红斑伴淡黄色分泌物。右附件肿块组织病理检查示恶性肿瘤*颗粒细胞瘤*,由短多边形细胞呈弥漫性片状排列,无模式。恶性细胞呈核沟状。未见坏死或其他卵巢肿瘤。输卵管和子宫内膜的组织病理学检查显示多发性结节性肉芽肿浸润。每个肉芽肿由多核巨细胞和上皮样细胞组成,周围环绕淋巴细胞,偶见中枢干酪化*生殖器结核*。结论:本病例报告的结论是强调要牢记生殖器结核作为卵巢癌的潜在鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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