De Luca F, Pandullo E, Polimeni A, Sindoni A, Gemelli M
Pediatrie. 1986 Jan-Feb;41(1):45-8.
The present case report concerns a male infant affected by congenital hypopituitarism presenting with neonatal hypoglycaemic attacks, microphallus and bilateral cryptorchidism. A transient cholestasis observed during the 2nd month of life and reversed by hydrocortisone treatment, is to be considered, in Authors' opinion, in the context of the endocrine syndrome, probably as consequence of the adrenal failure.
本病例报告涉及一名患有先天性垂体功能减退的男婴，表现为新生儿低血糖发作、小阴茎和双侧隐睾。作者认为，在出生后第2个月观察到的并通过氢化可的松治疗得以逆转的短暂性胆汁淤积，应在内分泌综合征的背景下考虑，可能是肾上腺功能衰竭的结果。
