Abdul-Rahman Omar A, Edghill Emma L, Kwan Andrea, Enns Gregory M, Hattersley Andrew T
Division of Medical Genetics, Department of Pediatrics, University of Mississippi Medical Center, Jackson, MS, USA.
J Pediatr Hematol Oncol. 2009 Jul;31(7):527-9. doi: 10.1097/MPH.0b013e3181a974c8.
Hypoplastic glomerulocystic kidney disease is an autosomal dominant disorder caused by mutations in hepatocyte nuclear factor-1beta. Hepatoblastoma is a sporadic occurring tumor of embryonal origin that has been associated with the several overgrowth syndromes. We report a case of concomitant hypoplastic glomerulocystic kidney disease and hepatoblastoma. Review of the literature identified 4 other patients with a similar association. We propose that hypoplastic glomerulocystic kidney disease and hepatoblastoma represent a possible association, and we excluded mutations in hepatocyte nuclear factor-1beta in our patient as causative of this putative association.
发育不全性肾小球囊性肾病是一种由肝细胞核因子-1β突变引起的常染色体显性疾病。肝母细胞瘤是一种散发的胚胎源性肿瘤,与多种过度生长综合征相关。我们报告了一例同时患有发育不全性肾小球囊性肾病和肝母细胞瘤的病例。文献回顾发现另外4例有类似关联的患者。我们提出发育不全性肾小球囊性肾病和肝母细胞瘤可能存在关联,并且在我们的患者中排除了肝细胞核因子-1β突变作为这种假定关联的病因。