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卵巢未成熟畸胎瘤后并发生长性畸胎瘤综合征和腹膜胶质瘤病:一例报告及文献复习

Coexisting growing teratoma syndrome and gliomatosis peritonei following ovarian immature teratoma: a case report and literature review.

作者信息

Türkmen Osman, Akar Inan Serra, Akbay Serap, Halilzade Mohammad İbrahim, Halilzade İnci, Moraloğlu Tekin Özlem

机构信息

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Faculty of Medicine, Ankara Yıldırım Beyazıt University, Ankara, Turkiye.

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Faculty of Medicine, University of Health Sciences, Ankara, Turkiye.

出版信息

Turk J Med Sci. 2024 Oct 7;54(6):1192-1197. doi: 10.55730/1300-0144.5899. eCollection 2024.

Abstract

Growing teratoma syndrome (GTS) is characterized by a reduction in serum tumor markers despite the growth of a benign mature teratomatous mass following chemotherapy for germ cell tumors. Gliomatosis peritonei (GP) typically accompanies ovarian teratomas, marked by the dissemination of mature glial tissue across the peritoneum. The concurrent presence of GTS and GP after treatment for ovarian immature teratoma (IMT) is notably rare, with approximately 20 reported cases. This case involves a 25-year-old patient who underwent surgical removal of an adnexal mass, which was later diagnosed as stage IIIA grade 3 ovarian IMT with parametrial involvement. Following two cycles of bleomycin, etoposide, and cisplatin chemotherapy, imaging identified new lesions adjacent to the liver and on the pelvic peritoneum. A second fertility-sparing surgery was performed, and paraffin pathology confirmed a mature teratoma within the excised specimen. Additionally, the resected pelvic peritoneum revealed nodules of mature glial tissue consistent with GP. The coexistence of GP with GTS post-IMT surgery presents a diagnostic challenge in distinguishing between malignant and benign components, which is critical to avoid unnecessarily aggressive surgical and chemotherapeutic treatments. Recognizing such cases may enable fertility-sparing surgery for these patients.

摘要

生长性畸胎瘤综合征(GTS)的特征是,在生殖细胞肿瘤化疗后,尽管良性成熟畸胎瘤肿块生长,但血清肿瘤标志物却降低。腹膜胶质瘤病(GP)通常伴随卵巢畸胎瘤出现,其特征是成熟神经胶质组织在腹膜扩散。卵巢未成熟畸胎瘤(IMT)治疗后同时出现GTS和GP的情况极为罕见,仅有约20例报道。该病例涉及一名25岁患者,其附件肿块经手术切除,随后被诊断为III A期3级卵巢IMT伴宫旁组织受累。在接受博来霉素、依托泊苷和顺铂化疗两个周期后,影像学检查发现肝脏附近和盆腔腹膜有新病变。进行了第二次保留生育功能的手术,石蜡病理证实切除标本内为成熟畸胎瘤。此外,切除的盆腔腹膜显示有与GP相符的成熟神经胶质组织结节。IMT手术后GP与GTS并存,在区分恶性和良性成分方面存在诊断挑战,这对于避免不必要的激进手术和化疗治疗至关重要。认识到这类病例可能使这些患者能够接受保留生育功能的手术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01d1/11673672/ca7f3f9e82e0/tjmed-54-06-1192f1.jpg

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