卵巢未成熟畸胎瘤的临床诊治策略

Clinical Diagnosis and Treatment Strategies for Ovarian Immature Teratoma

  • 摘要: 卵巢未成熟畸胎瘤(ovarian immature teratoma)是一种较为罕见的卵巢恶性肿瘤,好发于儿童、青少年及年轻成人。临床诊疗中,肿瘤标志物检测与影像学检查是鉴别成熟与未成熟畸胎瘤的重要依据,而术前行全面评估并据此选择适宜的手术方式与范围,是改善预后的关键。部分研究表明,对于Ⅰ期卵巢未成熟畸胎瘤,在严密随访下避免辅助化疗并不增加复发风险,也不影响患者远期生存;而晚期卵巢未成熟畸胎瘤仍建议术后行规范化疗。部分患者术后可能发生恶性生殖细胞成分良恶性转化,如生长性畸胎瘤综合征或鳞癌变等。由于卵巢未成熟畸胎瘤十分罕见,目前对其发病机制及临床管理的认知仍较为局限。本文围绕卵巢未成熟畸胎瘤的关键临床问题进行综述,并提出相应诊疗建议,以期为多学科协作与个体化治疗提供参考。

     

    Abstract: Ovarian immature teratoma is a relatively rare malignant ovarian tumor that predominantly occurs in children, adolescents, and young adults. In clinical diagnosis and treatment, tumor marker detection and imaging examinations serve as crucial bases for differentiating mature and immature terotomas. A comprehensive preoperative evaluation followed by the selection of an appropriate surgical approach and extent is key to improving prognosis. Some studies have indicated that for stage Ⅰ ovarian immature teratoma, avoiding adjuvant chemotherapy under close follow-up does not increase the risk of recurrence or affect long-term survival of patients; however, for advanced-stage ovarian immature teratoma, standardized postoperative chemotherapy is still recommended. Some patients may experience benign-malignant transformation of malignant germ cell components after surgery, such as growing teratoma syndrome or squamous cell carcinoma transformation. Due to the rarity of ovarian immature teratoma, current understanding of its pathogenesis and clinical management remains limited. This paper provides a review focusing on key clinical issues related to ovarian immature teratoma and proposes corresponding diagnostic and therapeutic recommendations, aiming to offer references for promoting multidisciplinary collaboration and individualized treatment.

     

/

返回文章
返回