Singh Vivek Kumar, Khanna Chitrali, Raman V Shankar, Goel Akhil
Department of Paediatric Surgery, Command Hospital (SC), Pune, Maharashtra, India.
Department of Surgery, Armed Forces Medical College, Pune, Maharashtra, India.
J Indian Assoc Pediatr Surg. 2022 Nov-Dec;27(6):764-767. doi: 10.4103/jiaps.jiaps_25_22. Epub 2022 Nov 14.
Pediatric adrenocortical tumors (ACTs) are rare entities with an incidence of 0.2% of all pediatric tumors. Only two cases of antenatally detected ACT have been reported in the literature. Our case is the first report of an antenatally detected suprarenal mass which manifested with postnatal virilizing features and was proven to be adrenocortical adenoma on histology.
小儿肾上腺皮质肿瘤(ACTs)是罕见的疾病,在所有小儿肿瘤中的发病率为0.2%。文献中仅报道过2例产前检测到的ACT。我们的病例是第一例关于产前检测到的肾上腺肿块的报告,该肿块在出生后表现出男性化特征,组织学检查证实为肾上腺皮质腺瘤。