Nozawa Akifumi, Ozeki Michio, Kawasaki Riko, Nakama Mina, Iwata Hisashi, Yamamoto Toshiyuki, Fukao Toshiyuki
Department of Pediatrics, Gifu University Graduate School of Medicine.
Gifu University School of Medicine.
J Pediatr Hematol Oncol. 2020 May;42(4):307-309. doi: 10.1097/MPH.0000000000001392.
Pleuropulmonary blastoma (PPB) is a rare, progressive, and aggressive malignant intrathoracic tumor observed during childhood. Mutations in the DICER1 gene have been considered a major etiologic factor of PPB and cause a variety of tumor types in children and young adults. We present a 3-year-old boy with type II PPB. Multimodal treatment consisting of surgery and neoadjuvant chemotherapy was effective. DICER1 mutations were examined by Sanger sequencing, microarray comparative genomic hybridization, and microsatellite markers. The results revealed that a somatic biallelic DICER1 mutation with uniparental disomy was present in the tumor tissue.
肺胸膜母细胞瘤(PPB)是一种在儿童期发现的罕见、进行性且侵袭性的胸腔内恶性肿瘤。DICER1基因的突变被认为是PPB的主要病因,可导致儿童和年轻成人出现多种肿瘤类型。我们报告了一名患有II型PPB的3岁男孩。由手术和新辅助化疗组成的多模式治疗是有效的。通过桑格测序、微阵列比较基因组杂交和微卫星标记对DICER1突变进行了检测。结果显示,肿瘤组织中存在具有单亲二体性的体细胞双等位基因DICER1突变。