Persistent Müllerian duct syndrome with testicular malignancy and unilateral seminal vesicle agenesis

Mehmet Ruhi Onur , Ahmet Kursad Poyraz , Ercan Kocakoç , Irfan Orhan
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引用次数: 1

Abstract

A 27-year-old male presented to our clinic for evaluation after operation which was made for a malignancy originated from undescended testis. Operation had revealed abdominal mass located right lateral to bladder originated from right testis. There were no additional findings at operation note. Pathology of specimen was mixed germ cell tumor consisting of embryonal carcinoma, yolk sac tumor and seminoma. Radiologic evaluation ultrasonography (US) showed a solid mass posterior to the bladder with a central cystic component and a hypoechoic oval shaped solid structure on the left side of this mass. Between these masses there was a hypoechoic band like structure. Magnetic resonance imaging (MRI) confirmed the presence of these masses. Four years after operation laboratory results revealed increased AFP levels and patient had exploratory laparotomy since a pelvic mass was seen on MRI and positron emission tomography (PET). Histopathologic diagnosis of tumor was embryonal carcinoma.

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持续性勒管综合征伴睾丸恶性肿瘤及单侧精囊发育不全
一名27岁男性病患,因睾丸肿大而行手术后,到本诊所求诊。手术发现腹部肿块位于膀胱右侧,起源于右侧睾丸。手术记录中无其他发现。标本病理为混合性生殖细胞瘤,由胚胎癌、卵黄囊瘤和精原细胞瘤组成。超声检查显示膀胱后方有一个实性肿块,中间有囊性成分,左侧有一个低回声的椭圆形实性结构。在这些团块之间有一个低回声带状结构。磁共振成像(MRI)证实了这些肿块的存在。手术后四年,实验室结果显示甲胎蛋白水平升高,由于MRI和正电子发射断层扫描(PET)发现盆腔肿块,患者进行了探查性剖腹探查。肿瘤组织病理诊断为胚胎癌。
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