Liver Unit.
Gastroenterology Department.
J Pediatr Gastroenterol Nutr. 2019 Apr;68(4):e54-e57. doi: 10.1097/MPG.0000000000002266.
McCune-Albright syndrome (MAS) results from a GNAS gene mutation. It is associated with café au lait macules, fibrous dysplasia, and several endocrinopathies to include gonadotropin-independent precocious puberty, growth hormone excess, Cushing syndrome, thyroid disease, and renal phosphate wasting. It is recognized to be a rare cause of neonatal cholestasis. We describe the hepatic outcome of 3 children with MAS referred to a single national liver unit. All presented with high gamma-glutamyl transpeptidase cholestasis and hepatitis. Cholestasis resolved by 1 year; but hepatic inflammation persisted, and 2 children developed progressive atypical focal nodular hyperplasia and 1 developed hepatoblastoma. This the first reported malignant hepatic lesion associated with MAS. MAS should be considered part of the differential diagnosis of neonatal cholestasis and affected children should be closely monitored for the development of hepatic lesions with regular liver ultrasound and alpha fetoprotein level.
McCune-Albright 综合征(MAS)是由 GNAS 基因突变引起的。它与咖啡牛奶斑、纤维结构不良以及多种内分泌疾病相关,包括促性腺激素依赖性性早熟、生长激素过多、库欣综合征、甲状腺疾病和肾脏磷酸盐丢失。它被认为是新生儿胆汁淤积的罕见原因。我们描述了 3 名 MAS 患儿的肝脏结局,这些患儿被转诊至单一的国家肝脏单位。所有患儿均表现为高γ-谷氨酰转肽酶胆汁淤积性肝炎。胆汁淤积在 1 年内缓解;但肝内炎症持续存在,其中 2 名患儿发展为进行性非典型局灶性结节性增生,1 名患儿发展为肝细胞癌。这是首例与 MAS 相关的恶性肝病变报道。MAS 应被视为新生儿胆汁淤积症鉴别诊断的一部分,应密切监测受影响患儿的肝脏病变的发展,包括定期进行肝脏超声和甲胎蛋白水平检查。