Meng J, Kang Y, Cheng H, Gu Y, Zhang X, Wang S
Eur J Gynaecol Oncol. 2016 Aug;37(4):587-590.
Krukenberg tumor with pregnancy is rare but it is a challenge for treatment and diagnosis. The authors report a case of a 29-week pregnant patient with a massive bilateral Krukenberg tumor which was misdiagnosed as myoma preoperatively and as ovarian stromal tumor intraoperatively. Prenatally the woman was asymptomatic except for preeclamptic symptoms, but red acne on the skin and elevated testosterone were observed. Pelvic ultrasound detected a heterogeneous solid mass mimicking a subserous myoma. The deterioration of preeclampsia prompted a cesarean section, but the neonate died nine days after he was born. A bilateral adnexal mass was found and considered as stromal tumor by frozen section because of luteinization of the stroma. The final pathology showed low differentiation adenocarcinoma of ovary, which was confirmed by gastric biopsies. The patient had undergone chemotherapy 16 times without surgical debulking and she was in generally well 1.5-year follow-up.
妊娠合并库肯勃瘤罕见,但对治疗和诊断来说是一项挑战。作者报告了一例29周妊娠的患者,其患有巨大双侧库肯勃瘤,术前被误诊为肌瘤,术中被误诊为卵巢间质瘤。产前该女性除有子痫前期症状外无其他症状,但观察到皮肤出现红色痤疮且睾酮升高。盆腔超声检测到一个异质性实性肿块,类似浆膜下肌瘤。子痫前期病情恶化促使进行剖宫产,但新生儿出生九天后死亡。发现双侧附件肿块,由于间质黄素化,冰冻切片考虑为间质瘤。最终病理显示为低分化卵巢腺癌,经胃活检确诊。该患者未进行手术减瘤,已接受16次化疗,随访1.5年,总体情况良好。