Storr Helen L, Barwick Tara D, Snodgrass Graeme A I, Booy Robert, Morel Yves, Reznek Rodney H, Savage Martin O
Department of Endocrinology, St Bartholomew's and The Royal London School of Medicine and Dentistry, London, UK.
Horm Res. 2003;60(2):99-102. doi: 10.1159/000071878.
We report the case of a child with congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency, with hyperplasia of adrenal rest tissue presenting as a retroperitoneal mass. Complete resolution of the mass was noted after 18 months of hydrocortisone replacement therapy.
我们报告了一例因11β-羟化酶缺乏导致先天性肾上腺增生的儿童病例,其肾上腺残余组织增生表现为腹膜后肿块。在接受氢化可的松替代治疗18个月后,肿块完全消退。