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Metachronous Type I pleuropulmonary blastoma and atypical choroid plexus papilloma in a young child

机译:幼儿期I型胸膜肺母细胞瘤和非典型脉络丛乳头状瘤

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摘要

Pleuropulmonary blastoma (PPB) is a rare childhood tumor, often associated with germline DICER1 mutations and a risk for development of other benign and malignant tumors, a constellation termed DICER1 syndrome. A 1-year-old male was diagnosed with Type I PPB and screened regularly thereafter for detection of intrathoracic and intraabdominal disease. Ten months after diagnosis of PPB, he presented with headaches and vomiting. He was diagnosed with atypical choroid plexus papilloma, a lesion not previously reported with PPB. The presence of central nervous system symptoms in patients with PPB or a phenotype suggestive of DICER1 syndrome should prompt early intracranial imaging.
机译:胸膜肺母细胞瘤(PPB)是一种罕见的儿童期肿瘤,通常与种系DICER1突变相关,并有发展成其他良性和恶性肿瘤的危险,这种星座称为DICER1综合征。一名1岁男性被诊断患有I型PPB,此后定期进行筛查以检测胸腔和腹腔疾病。诊断为PPB十个月后,他出现头痛和呕吐。他被诊断出患有非典型脉络丛乳头状瘤,这是PPB以前没有报道的病变。 PPB或表型提示DICER1综合征的患者中枢神经系统症状的出现应促使早期颅内成像。

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