Zong Xuan, Yang Jia-Xin, Zhang Ying, Cao Dong-Yan, Shen Keng, You Yan, Guo Li-Na
Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China,
Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Onco Targets Ther. 2019 Mar 28;12:2365-2372. doi: 10.2147/OTT.S192111. eCollection 2019.
46, XY pure gonadal dysgenesis (PGD) is characterized as a female phenotype with strip-like gonads, which has a high tendency to develop into gonadal tumors. Somatic-type malignancies of germ cell tumors (SMs of GCTs) refer to the presence of malignant non-germ cell histologies admixed with GCTs, which are usually chemoresistant and indicate poor prognosis. This case report aimed to analyze the special histological type of GCTs and the importance of salvage surgery in the treatment of refractory GCTs. We report a unique case of gonadal yolk sac tumor (YST) transformed into SMs in a patient with 46, XY PGD. This 18-year-old woman underwent laparoscopic pelvic tumor resection, considered her first surgery, 2 years ago, and pathology revealed YST with initial alpha-fetoprotein (AFP) level measuring >3,000 ng/mL. She underwent seven cycles of chemotherapy, and the AFP level decreased to within a normal range after the second cycle. However, a computed tomography scan after the seventh cycle revealed abdominal and pelvic metastases, and vaginal bleeding was continuously observed. Laparoscopic exploration and laparotomy with tumor subtotal resection were performed. A pathology report showed SMs (sarcoma) derived from YST. Whole exome sequencing demonstrated that the main somatic mutation was a non-synonymous mutation of (c.182A>G), and this result did not show any indications for targeted drugs. She received three cycles of PEI (cisplatin, etoposide, and ifosfamide) chemotherapy but showed no response. She refused to undergo further treatment and has been alive with the disease for 7 months. This suggests that SMs may be one of the reasons for chemoresistance of refractory GCTs, and salvage surgery may be one of the most effective treatments for this patient. Targeted therapy may be a new choice for chemoresistant GCTs, but drug selection must be based on gene sequencing, and its efficacy still needs to be verified by further study.
46,XY单纯性腺发育不全(PGD)的特征是具有条索状性腺的女性表型,其发展为性腺肿瘤的倾向很高。生殖细胞肿瘤的体细胞型恶性肿瘤(GCTs的SMs)是指与GCTs混合存在的恶性非生殖细胞组织学类型,通常对化疗耐药且预后不良。本病例报告旨在分析GCTs的特殊组织学类型以及挽救性手术在难治性GCTs治疗中的重要性。我们报告了一例46,XY PGD患者性腺卵黄囊瘤(YST)转化为SMs的独特病例。这位18岁女性在2年前接受了腹腔镜盆腔肿瘤切除术,被视为首次手术,病理显示为YST,初始甲胎蛋白(AFP)水平>3000 ng/mL。她接受了7个周期的化疗,第二个周期后AFP水平降至正常范围。然而,第七个周期后的计算机断层扫描显示腹部和盆腔转移,且持续观察到阴道出血。进行了腹腔镜探查和肿瘤次全切除的剖腹手术。病理报告显示为源自YST的SMs(肉瘤)。全外显子测序表明主要体细胞突变是(c.182A>G)的非同义突变,该结果未显示任何靶向药物的指征。她接受了3个周期的PEI(顺铂、依托泊苷和异环磷酰胺)化疗但无反应。她拒绝进一步治疗,带瘤生存7个月。这表明SMs可能是难治性GCTs化疗耐药的原因之一,挽救性手术可能是该患者最有效的治疗方法之一。靶向治疗可能是化疗耐药GCTs的新选择,但药物选择必须基于基因测序,其疗效仍需进一步研究验证。