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颗粒细胞瘤:联合药物-手术治疗后两次自然妊娠:病例报告及文献复习。

Granulosa tumor: two spontaneous pregnancies after combined medico-surgical treatment: case report and review of the literature.

机构信息

Hôpital Louis Mourier (Colombes) -AP-HP, Nord-Université de Paris Cité, Colombes, France.

Hôpital Bichat - Claude Bernard (Paris) -AP-HP, Nord-Université de Paris Cité, Paris, France.

出版信息

J Med Case Rep. 2023 Mar 30;17(1):135. doi: 10.1186/s13256-023-03793-5.

Abstract

BACKGROUND

Granulosa tumor is a rare tumor that arises from the mesenchyme and the sexual cord of the ovary. The prognosis is generally excellent, and treatment is mainly based on surgery, followed by chemotherapy depending on the extension of the disease. However, "the obstetrical prognosis" is compromised.

CASE PRESENTATION

We report the case of a 32-year-old Caucasian patient who was diagnosed during a primary infertility assessment with an ultrasound image of a 39 mm organic left ovarian cyst confirmed on pelvic magnetic resonance imaging with infiltration of the uterosacral space. Tumor markers, including cancer antigen 125, alpha fetoprotein, and β-human chorionic gonadotropin, were normal. Histological study of biopsies of the ovarian lesion taken during exploratory laparoscopy confirmed the diagnosis of adult granulosa tumor. After a normal extension assessment including a thoracoabdominopelvic computed tomography scan and a positron emission tomography scan, the patient underwent complete conservative surgery and the disease was classified as stage Ic. Three cycles of adjuvant chemotherapy according to the "BEP" protocol combining bleomycin, etoposide, and cisplatin were performed after oocyte cryopreservation. After a 5-year follow-up period, the patient had no sign of tumor progression and had two spontaneous pregnancies, the first occurring 3 months after the end of chemotherapy and the second 14 months later.

CONCLUSION

Granulosa cell tumor remains a rare tumor whose management considerably compromises fertility and reduces the chances of having a spontaneous pregnancy. The particularity of our observation is that the diagnosis of the granulosa tumor was made following a primary infertility assessment and that the patient had two spontaneous pregnancies 3 months after the end of a medico-surgical treatment known to be very gonadotoxic.

摘要

背景

颗粒细胞瘤是一种罕见的肿瘤,起源于卵巢的间质和性索。预后通常良好,治疗主要基于手术,根据疾病的扩展情况,随后进行化疗。然而,“产科预后”受到影响。

病例介绍

我们报告了一例 32 岁的白人患者,在原发性不孕评估中,超声图像显示左侧卵巢 39 毫米有机囊肿,经盆腔磁共振成像证实,并浸润了子宫骶骨间隙。肿瘤标志物,包括癌抗原 125、甲胎蛋白和β-人绒毛膜促性腺激素,均正常。腹腔镜探查活检的组织学研究证实了成人颗粒细胞瘤的诊断。在进行包括胸腹部盆腔计算机断层扫描和正电子发射断层扫描的扩展评估后,患者接受了完全的保守性手术,疾病被分类为 Ic 期。在卵母细胞冷冻保存后,根据联合使用博来霉素、依托泊苷和顺铂的“BEP”方案进行了三个周期的辅助化疗。经过 5 年的随访期,患者没有肿瘤进展的迹象,并自然怀孕了两次,第一次是在化疗结束后 3 个月,第二次是在 14 个月后。

结论

颗粒细胞瘤仍然是一种罕见的肿瘤,其管理极大地影响了生育能力,并降低了自然怀孕的机会。我们观察的特殊性在于,颗粒细胞瘤的诊断是在原发性不孕评估后做出的,并且患者在接受了一种已知非常性腺毒性的医学-手术治疗后 3 个月自然怀孕了两次。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7665/10061986/ca6410faa77b/13256_2023_3793_Fig1_HTML.jpg

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