Subramanian Subramanian, Gamanagatti Shivanand, Sharma Raju
Department of Radiodiagnosis, All India Institute of Medical Sciences, New Delhi 110029, India.
Pediatr Radiol. 2006 Nov;36(11):1194-6. doi: 10.1007/s00247-006-0280-5. Epub 2006 Aug 16.
We present the rare case of a 14-year-old female pseudohermaphrodite due to congenital adrenal hyperplasia (CAH). MRI revealed the presence of a hypoplastic uterus, ovaries, clitoromegaly, and prostate gland with its typical zonal anatomy. Transrectal sonography also confirmed the presence of a prostate gland.
我们报告了一例罕见的因先天性肾上腺增生(CAH)导致的14岁女性假两性畸形病例。磁共振成像(MRI)显示存在发育不全的子宫、卵巢、阴蒂肥大以及具有典型分区解剖结构的前列腺。经直肠超声检查也证实了前列腺的存在。