Kamoun Salma, Charfi Lamia, Doghri Raoudha, Driss Maha, Boujelbene Nadia, Abess Imen, Mrad Karima
Service d'anatomie et cytologie pathologiques, institut Salah Azaiez, boulevard 9 Avril 1938, 1006 Bab Saadoun, Tunis, Tunisie.
Service d'anatomie et cytologie pathologiques, institut Salah Azaiez, boulevard 9 Avril 1938, 1006 Bab Saadoun, Tunis, Tunisie.
Ann Pathol. 2023 Sep;43(5):400-406. doi: 10.1016/j.annpat.2023.01.018. Epub 2023 Feb 24.
Sex cord tumor with annular tubules (SCTAT) is a rare ovarian tumor. It belongs to sex cord and stromal tumor of the ovary and represents less than 1% of cases. It includes two forms: the first one associated with Peuz-Jeghers syndrome and the second sporadic. We report 4 cases of SCTAT collected at the department of pathology of Salah Azaiez Institute of Tunis over the 12 last years. The age ranged from 10 to 32 years. Symptoms were non specific except for one case revealed by precocious puberty. One patient had Peutz-Jeghers syndrome associated. Tumors were unilateral. Gross findings showed often a solid tumor with yellow cut surface. Their size ranged from 0.5cm to 28cm. Their morphological features were characteristic. Immunohistochemistry showed that tumor cells expressed inhibin and claretinin. The treatment was surgical, often conservative. The diagnosis of malignancy wasn't focused on histological features, but on tumor extension, clinical course, and presence of metastases. Evolution was often favorable. We also performed a systematic review of the literature that identified 166 cases. Features of these cases were studied. We also compared these features between sporadic and syndromic forms and between benign and malignant forms. In conclusion, SCTAT is a rare tumor, usually benign. Its diagnosis is based on histological examination. There is a malignant potential especially in sporadic forms, estimated at 20%. Treatment is most often conservative, based on oophorectomy.
伴有环状小管的性索肿瘤(SCTAT)是一种罕见的卵巢肿瘤。它属于卵巢性索间质肿瘤,病例占比不到1%。它包括两种类型:第一种与佩-吉综合征相关,第二种为散发性。我们报告了突尼斯萨拉赫·阿扎耶兹研究所病理科在过去12年中收集的4例SCTAT病例。年龄范围为10至32岁。除1例因性早熟发现外,症状均不具有特异性。1例患者伴有佩-吉综合征。肿瘤均为单侧。大体检查常显示为实性肿瘤,切面呈黄色。其大小从0.5厘米至28厘米不等。其形态学特征具有特异性。免疫组化显示肿瘤细胞表达抑制素和钙视网膜蛋白。治疗方式为手术,通常采用保守治疗。恶性诊断并非基于组织学特征,而是基于肿瘤的扩展、临床病程及转移情况。病情发展通常较好。我们还对文献进行了系统回顾,共识别出166例病例。对这些病例的特征进行了研究。我们还比较了散发性和综合征性类型之间以及良性和恶性类型之间的这些特征。总之,SCTAT是一种罕见肿瘤,通常为良性。其诊断基于组织学检查。存在恶性潜能,尤其是散发性类型,估计为20%。治疗最常采用保守治疗,即卵巢切除术。