首页> 外文期刊>American journal of medical genetics, Part A >Hepatoblastoma and heart transplantation in a patient with cardio-facio-cutaneous syndrome.
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Hepatoblastoma and heart transplantation in a patient with cardio-facio-cutaneous syndrome.

机译:心脏-面部皮肤综合征患者的肝母细胞瘤和心脏移植。

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摘要

Cardio-facio-cutaneous syndrome (CFC) and Costello syndrome (CS) are disorders with an overlapping spectrum of congenital anomalies. Mutations in the RAS-MAPK pathway have recently been reported in both of these syndromes, with HRAS mutations characteristic for CS and BRAF and MEK1/2 mutations for CFC. We report on a 3-year-old boy who underwent a cardiac transplant at age 8 months for hypertrophic cardiomyopathy; he was subsequently suspected to have CS. At age 35 months he presented with an intra-cardiac mass that was diagnosed as metastatic hepatoblastoma. Although hepatoblastoma is not known to have an increased frequency in immunocompromised patients, questions were raised as whether the post-transplant immuno-suppressive therapy played a role in tumor development. The patient died shortly thereafter and his post-mortem DNA analysis revealed a MEK1 mutation (Y130C) previously reported in CFC. While CS is associated with increased cancer risk, only a single case of leukemia has been reported in a patient with CFC, making this the first case of a solid tumor reported in a patient with CFC.
机译:心脏面部皮肤综合征(CFC)和科斯特洛综合征(CS)是先天性异常频谱重叠的疾病。最近在这两种综合征中都报道了RAS-MAPK途径的突变,其中CS和BRAF具有HRAS突变特征,CFC具有MEK1 / 2突变特征。我们报道了一个3岁男孩,他在8个月大时因肥厚型心肌病接受了心脏移植。他随后被怀疑患有CS。在35个月大时,他出现了心脏内肿块,被诊断为转移性肝母细胞瘤。尽管尚不知道肝母细胞瘤在免疫功能低下患者中的发生率会增加,但还是提出了问题,例如移植后免疫抑制疗法是否在肿瘤发展中起作用。该患者此后不久死亡,他的验尸DNA分析显示以前在CFC中报告过MEK1突变(Y130C)。虽然CS与增加的癌症风险相关,但仅在CFC患者中报告了一例白血病,这使其成为CFC患者中报告的第一例实体瘤。

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