Ito Mitsuhiro, Hashizume Kohei, Kanamori Yutaka
Department of Pediatric Surgery, University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655 Japan.
Int J Urol. 2004 Feb;11(2):125-7. doi: 10.1111/j.1442-2042.2004.00744.x.
We present the extremely rare phenotype of an accessory scrotum with an associated lipoblastoma. There was a coexistence of midperineal and lateral types. To our knowledge, this phenotype has never been reported. The lipoblastoma, which arose in the perineum, divided the moving labioscrotal swelling into three parts during early fetal life. This resulted in the specific anomaly in this patient.
我们报告了一种极为罕见的伴有脂肪母细胞瘤的副阴囊表型。存在会阴中部型和外侧型并存的情况。据我们所知,这种表型从未有过报道。起源于会阴的脂肪母细胞瘤在胎儿早期将移动的阴唇阴囊肿胀分为三部分。这导致了该患者出现特定的异常情况。