Nonvirilized external genitalia in a Nigerian female neonate with salt-wasting congenital adrenal hyperplasia

E. Oyenusi, Funmilayo Babatunde, Pauline Akowundu, Uzoamaka Nwigbo, A. Oduwole
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Abstract

A 3-week-old female neonate presented with complaints of weakness and inability to feed. She had been delivered at a general hospital with a birth weight of 3.3 kg. She had jaundice, which was treated with phototherapy and resolved after 3 days. Pregnancy and delivery were uneventful. Parents identified her as female. Examination revealed hanging skin folds, dehydration, tachycardia, hyperpigmentation and swelling of the labial folds, no clitoromegaly, and no palpable gonads. She had lost 30% of her birth weight and was hypoglycemic. Serum investigations showed hyponatremia, metabolic acidosis, hyperkalemia, and hypocortisolemia with elevated testosterone and 17-hydroxyprogesterone. Pelvic ultra sound scan showed normal-sized uterus and no testes suggesting a diagnosis of salt-wasting congenital adrenal hyperplasia (CAH). She is being managed with hydrocortisone, fludrocortisone, and added salt to feeds. Labial swelling and hyperpigmentation have resolved and external genitalia is typically female in appearance. She is gaining weight and thriving. Salt-wasting CAH can present with adrenal crisis without obvious virilization of the external genitalia in the female neonate and can be diagnosed by scrutiny of electrolytes in the sick neonate.
非男性化的外生殖器在尼日利亚女性新生儿与盐耗性先天性肾上腺增生
一名三周大的女婴表现出虚弱和无法进食的症状。她是在一家综合医院出生的,出生体重为3.3公斤。患者有黄疸,经光疗治疗,3天后消退。怀孕和分娩都平安无事。父母确认她是女性。检查发现皮肤褶皱下垂,脱水,心动过速,色素沉着,唇襞肿胀,未见阴蒂肿大,未见性腺。她的出生体重下降了30%,并且出现了低血糖。血清调查显示低钠血症、代谢性酸中毒、高钾血症和低皮质醇血症伴睾酮和17-羟孕酮升高。盆腔超声检查显示子宫大小正常,未见睾丸,提示诊断为耗盐型先天性肾上腺增生症。她正在接受氢化可的松、氟化可的松治疗,并在饲料中添加盐。阴唇肿胀和色素沉着已经消失,外生殖器的外观是典型的女性。她的体重在增加,身体也在茁壮成长。在女性新生儿中,盐耗性CAH可以表现为肾上腺危象,但没有明显的外生殖器男性化,可以通过检查患病新生儿的电解质来诊断。
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