Abdelmeguid Yasmine, Yakout Nada, Oshiba Ahmed, Zain Mostafa, Kotb Mostafa
Department of Pediatric Endocrinology, Alexandria Faculty of Medicine, Alexandria, Egypt.
Department of Pathology, Alexandria Faculty of Medicine, Alexandria, Egypt.
Clin Pediatr Endocrinol. 2021;30(1):57-60. doi: 10.1297/cpe.30.57. Epub 2021 Jan 5.
Congenital adrenal hyperplasia is the most common cause of ambiguous genitalia worldwide, with an incidence of 1 in 15,000 live births. The most frequently-occurring subtype, 21-hydroxylase deficiency, results in diminished production of aldosterone and cortisol as well as increased androgen secretion. Previous studies have reported a relationship between ovarian cyst formation and adrenal androgen excess; nevertheless, neonatal large ovarian cysts have rarely been reported in newborns with congenital adrenal hyperplasia. Herein, we present the unique case of a neonate with classical 21-hydroxylase deficiency who underwent surgery for a huge unilateral solitary ovarian follicular cyst on the seventh postnatal day. Possible mechanisms by which androgen excess may cause ovarian cyst formation are also discussed.
先天性肾上腺皮质增生症是全球范围内导致生殖器模糊最常见的原因,活产婴儿中的发病率为1/15000。最常见的亚型是21-羟化酶缺乏症,会导致醛固酮和皮质醇分泌减少以及雄激素分泌增加。既往研究报道了卵巢囊肿形成与肾上腺雄激素过多之间的关系;然而,先天性肾上腺皮质增生症新生儿中罕见新生儿大卵巢囊肿的报道。在此,我们报告了一例典型21-羟化酶缺乏症新生儿的独特病例,该患儿在出生后第7天因巨大单侧孤立性卵巢滤泡囊肿接受了手术。本文还讨论了雄激素过多可能导致卵巢囊肿形成的潜在机制。