Lee Eunhyun, Park Minjeong
Department of Obstetrics and Gynecology, Inje University Haeundae Paik Hospital, Busan, Republic of Korea.
Case Rep Oncol. 2023 Mar 15;16(1):157-161. doi: 10.1159/000529838. eCollection 2023 Jan-Dec.
Primary ovarian neuroendocrine carcinoid tumors are extremely rare. However, their clinical course is good, and hence, fertility-sparing surgery is a feasible treatment option in cases of unilateral localized lesions. In this report, we present the case of a 20-year-old nulliparous woman who was diagnosed as having a primary ovarian neuroendocrine carcinoid tumor arising from a mature cystic teratoma. She underwent laparoscopic right ovarian cystectomy, and her postoperative recovery was uneventful. The patient has been under close observation over a 1-year follow-up period and has shown no evidence of tumor recurrence.
原发性卵巢神经内分泌类癌肿瘤极为罕见。然而,其临床病程良好,因此,对于单侧局限性病变的病例,保留生育功能的手术是一种可行的治疗选择。在本报告中,我们介绍了一名20岁未生育女性的病例,该患者被诊断为起源于成熟囊性畸胎瘤的原发性卵巢神经内分泌类癌肿瘤。她接受了腹腔镜下右卵巢囊肿切除术,术后恢复顺利。该患者在1年的随访期内一直接受密切观察,未发现肿瘤复发迹象。