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Segmental storiform collagenomas: Expanding the spectrum of PTEN PTEN hamartoma tumor syndrome in children

机译:节段储层胶原蛋白:扩展儿童Pten Pten Hamartoma肿瘤综合征的谱

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Abstract A 4‐year‐old girl with autism spectrum disorder and congenital heart disease presented to dermatology clinic for?evaluation of skin growths present since infancy. Physical examination was significant for macrocephaly and agminated skin‐colored to pink papulonodules in a segmental distribution on the right lower back and buttocks, biopsy of which showed storiform collagenomas (sclerotic fibromas). Genetic testing revealed a pathogenic missense mutation in the PTEN gene, and a diagnosis of PTEN hamartoma tumor syndrome was made. The segmental nature of her storiform collagenomas is unique, to our knowledge, and may be explained by a postzygotic second‐hit PTEN mutation, contributing to the growing spectrum of clinical findings associated with PTEN hamartoma tumor syndrome.
机译:摘要一个4岁的女孩患有自闭症谱系障碍和先天性心脏病,呈现给皮肤科诊所?评估自婴儿婴儿以来的皮肤生长。 体格检查对于大型畸形和粉状粉迹的粉末粉迹,在右下后背部和臀部的节段分布中,其活检显示,其显示储层胶原蛋白酶(硬化纤维纤维素)。 基因检测揭示了PTEN基因中的致病畸变突变,并进行了PTEN HARARTOMA肿瘤综合征的诊断。 她的储层胶原蛋白酶的分段性是我们知识的独特性,并且可以通过Postygotic第二次突变的PTEN突变来解释,促进与PTEN HARARTOMA肿瘤综合征相关的临床发现的繁殖范围。

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