Deguchi Koichi, Tazuke Yuko, Watanabe Miho, Toyama Chiyoshi, Nomura Motonari, Saka Ryuta, Harada Hiromi, Nagamine Yukie, Endo Masayuki, Puh Ritsuko, Okuyama Hiroomi
Department of Pediatric Surgery, Graduate School of Medicine, Osaka University.
Center for Maternal, Fetal and Neonatal Medicine, Osaka University Hospital.
Radiol Case Rep. 2022 Jan 12;17(3):881-885. doi: 10.1016/j.radcr.2021.12.033. eCollection 2022 Mar.
Accessory scrotum (AS) is rarely diagnosed antenatally, and its prenatal features remain unknown. Here, we report a case of a prenatally diagnosed accessory scrotum with perineal lipoma. A 33-year-old woman was referred to our hospital at 35 weeks of gestation to evaluate a mass in the fetal perineal region. Prenatal ultrasonography showed a 2.0 × 2.0 cm sized, echogenic, and circular mass located posterior to the left scrotum in a male fetus. Magnetic resonance imaging (MRI) showed a mass containing adipose tissue. A 6.5 cm elastic mass (AS and protruding lipoma) was observed in the perineal region, and surgical excision was performed at 8 months of age. Histological examination confirmed the diagnosis of AS with perineal lipoma, and there was no recurrence at follow-up. The typical prenatal presentation of AS was a circular perineal mass located posterior to the normal scrotum and was associated with perineal lipoma. The prenatal detection of AS was feasible with careful observation via ultrasonography, and prenatal MRI was useful in characterizing perineal tumors and evaluating associated anomalies.
副阴囊(AS)在产前很少被诊断出来,其产前特征仍不为人知。在此,我们报告一例产前诊断为副阴囊合并会阴脂肪瘤的病例。一名33岁女性在妊娠35周时被转诊至我院,以评估胎儿会阴区的肿物。产前超声检查显示,一名男性胎儿的左阴囊后方有一个大小为2.0×2.0 cm、呈高回声的圆形肿物。磁共振成像(MRI)显示一个包含脂肪组织的肿物。在会阴区观察到一个6.5 cm的弹性肿物(副阴囊和突出的脂肪瘤),并在患儿8个月大时进行了手术切除。组织学检查证实诊断为副阴囊合并会阴脂肪瘤,随访期间无复发。副阴囊典型的产前表现是位于正常阴囊后方的圆形会阴肿物,并与会阴脂肪瘤相关。通过超声仔细观察,产前检测副阴囊是可行的,产前MRI有助于对会阴肿瘤进行特征性描述并评估相关异常情况。