Murase Naruhiko, Uchida Hiroo, Hiramatsu Kiyoshi
Department of Pediatric Surgery, Anjo Kosei Hospital, Anjo, Japan ; Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Nagoya J Med Sci. 2015 Aug;77(3):501-6.
We report a case of accessory scrotum (AS) in the perineal region with peduncular lipoma, diagnosed prenatally. A male fetus of 31 weeks' gestation was referred to our department with a perineal mass. Prenatal ultrasonography and magnetic resonance imaging showed a mass of 1.0 × 1.2 cm located posterior to the scrotum. No other abnormalities were noted during pregnancy. The patient was delivered vaginally at 38 weeks of gestation. On physical examination, a soft peduncular mass with a rugged and pigmented swelling was located between the normally developed scrotum and the anus. There were no specific symptoms or any other associated congenital anomalies. We completely excised the mass at one month of age. A histological examination revealed lipoma, with tissue suggestive of scrotum, so a definite diagnosis of AS was made. AS is a rare congenital anomaly of the scrotum. We review the literature.
我们报告一例产前诊断的会阴区带蒂脂肪瘤的副阴囊(AS)病例。一名孕31周的男性胎儿因会阴肿物转诊至我科。产前超声和磁共振成像显示阴囊后方有一个1.0×1.2 cm的肿物。孕期未发现其他异常。该患者在孕38周时经阴道分娩。体格检查发现,在正常发育的阴囊和肛门之间有一个柔软的带蒂肿物,表面粗糙且有色素沉着。无特殊症状或其他相关先天性异常。患儿1月龄时我们将肿物完整切除。组织学检查显示为脂肪瘤,伴有提示阴囊的组织,因此确诊为AS。AS是一种罕见的阴囊先天性异常。我们对相关文献进行了综述。