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两名儿科患者的科斯特洛综合征与脐韧带横纹肌肉瘤:病例报告及文献综述

Costello Syndrome and Umbilical Ligament Rhabdomyosarcoma in Two Pediatric Patients: Case Reports and Review of the Literature.

作者信息

Sánchez-Montenegro Carlos, Vilanova-Sánchez Alejandra, Barrena-Delfa Saturnino, Tenorio Jair, Santos-Simarro Fernando, García-Miñaur Sixto, Lapunzina Pablo, Martínez-Martínez Leopoldo

机构信息

Pediatric Surgical Oncology Section, Oncology Service, Department of Hematology-Oncology, Hospital Nacional de Niños "Dr. Carlos Sáenz Herrera", Paseo Colón, 1654-1000 San José, Costa Rica; Oncology Section, Department of Pediatric Surgery, Hospital Universitario La Paz, Paseo de la Castellana 261, 28046 Madrid, Spain.

Oncology Section, Department of Pediatric Surgery, Hospital Universitario La Paz, Paseo de la Castellana 261, 28046 Madrid, Spain.

出版信息

Case Rep Genet. 2017;2017:1587610. doi: 10.1155/2017/1587610. Epub 2017 Jan 19.

Abstract

Costello syndrome is caused by heterozygous de novo missense mutations in the protooncogene with tumor predisposition, especially rhabdomyosarcoma. We here report two pediatric patients with Costello syndrome and umbilical ligament rhabdomyosarcoma. A review of the literature published in English in MEDLINE from January 1971 to June 2016 using the search terms "Costello syndrome" and "rhabdomyosarcoma" was performed, including two new cases that we describe. Twenty-six patients with Costello syndrome and rhabdomyosarcoma were recorded with mean age of diagnosis of 2 years and 8 months. The most common tumor location was the abdomen/pelvis, including four out of ten of those in the umbilical ligament. The most common histological subtype was embryonal rhabdomyosarcoma. Overall survival was 43%. A total of 17 rhabdomyosarcomas in pediatric patients arising in the umbilical ligament were recorded with mean age of diagnosis of 3 years and 4 months. Overall survival was 69%. Costello syndrome is a poorly known disorder in pediatric oncology but their predisposition to malignancies implies the need for a new perspective on early diagnosis and aggressive medical and surgical treatment.

摘要

科斯特洛综合征由原癌基因中的杂合性新发错义突变引起,具有肿瘤易感性,尤其是横纹肌肉瘤。我们在此报告两名患有科斯特洛综合征和脐韧带横纹肌肉瘤的儿科患者。我们使用检索词“科斯特洛综合征”和“横纹肌肉瘤”对1971年1月至2016年6月期间MEDLINE上发表的英文文献进行了回顾,包括我们描述的两例新病例。记录了26例患有科斯特洛综合征和横纹肌肉瘤的患者,诊断时的平均年龄为2岁8个月。最常见的肿瘤部位是腹部/骨盆,其中十分之四位于脐韧带。最常见的组织学亚型是胚胎型横纹肌肉瘤。总生存率为43%。记录了17例儿科患者发生在脐韧带的横纹肌肉瘤,诊断时的平均年龄为3岁4个月。总生存率为69%。科斯特洛综合征在儿科肿瘤学中是一种鲜为人知的疾病,但他们对恶性肿瘤的易感性意味着需要对早期诊断以及积极的药物和手术治疗有新的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0da9/5288506/74de28622a1a/CRIG2017-1587610.001.jpg

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