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一名幼儿同时患两种肿瘤。

A concurrent episode of two neoplasms in a toddler-age child.

作者信息

Alrazzak Muaz A, Zablahalabi Jenny, Alrazzak Baraa, De Angulo Guillermo

机构信息

Department of Pediatrics, Roswell Park Cancer Institute, Buffalo, New York, United States.

Department of Pediatrics, Miami Children's Hospital, Miami, Florida, United States.

出版信息

Avicenna J Med. 2014 Apr;4(2):48-50. doi: 10.4103/2231-0770.130347.

DOI:10.4103/2231-0770.130347
PMID:24761385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3994710/
Abstract

Childhood neoplasms are relatively rare and represent only about 1- 2% of the total incidence of neoplasms in United States. Concurrent episode of childhood cancer is uncommon and usually related to a cancer genetic syndrome. Li Fraumeni Syndrome refers to an autosomal dominant condition that is manifested by the development of certain cancers in early childhood and an increased lifetime risk for developing multiple primary cancers including sarcoma, breast cancer, leukemia, bone cancer, and others. We report a case of a 21-month-old girl who was found to have orbital embryonal rhabdomyosarcoma and adrenocortical tumor concurrently.

摘要

儿童肿瘤相对罕见,仅占美国肿瘤总发病率的约1%-2%。儿童癌症并发情况并不常见,通常与癌症遗传综合征有关。李-弗劳梅尼综合征是一种常染色体显性疾病,表现为儿童早期发生某些癌症,以及患多种原发性癌症(包括肉瘤、乳腺癌、白血病、骨癌等)的终生风险增加。我们报告一例21个月大女童,其同时被发现患有眼眶胚胎性横纹肌肉瘤和肾上腺皮质肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ae/3994710/d246618a470a/AJM-4-48-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ae/3994710/206e2c602465/AJM-4-48-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ae/3994710/d246618a470a/AJM-4-48-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ae/3994710/206e2c602465/AJM-4-48-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ae/3994710/d246618a470a/AJM-4-48-g002.jpg

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1
A concurrent episode of two neoplasms in a toddler-age child.一名幼儿同时患两种肿瘤。
Avicenna J Med. 2014 Apr;4(2):48-50. doi: 10.4103/2231-0770.130347.
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本文引用的文献

1
Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study.胚系 TP53 突变携带者 Li-Fraumeni 综合征的生化和影像学监测:一项前瞻性观察研究。
Lancet Oncol. 2011 Jun;12(6):559-67. doi: 10.1016/S1470-2045(11)70119-X. Epub 2011 May 19.
2
Gastric cancer in individuals with Li-Fraumeni syndrome.Li-Fraumeni 综合征患者的胃癌。
Genet Med. 2011 Jul;13(7):651-7. doi: 10.1097/GIM.0b013e31821628b6.
3
Inherited cancer syndromes in children and young adults.儿童和青年的遗传性癌症综合征。
J Pediatr Hematol Oncol. 2010 Apr;32(3):195-228. doi: 10.1097/MPH.0b013e3181ced34c.
4
2009 version of the Chompret criteria for Li Fraumeni syndrome.2009年版李-弗劳梅尼综合征的乔普雷标准。
J Clin Oncol. 2009 Sep 10;27(26):e108-9; author reply e110. doi: 10.1200/JCO.2009.22.7967. Epub 2009 Aug 3.
5
TP53 germline mutations in Portugal and genetic modifiers of age at cancer onset.葡萄牙的 TP53 种系突变与癌症发病年龄的遗传修饰因子。
Fam Cancer. 2009;8(4):383-90. doi: 10.1007/s10689-009-9251-y. Epub 2009 May 26.
6
Orbital rhabdomyosarcoma in Li-Fraumeni syndrome.李-弗劳梅尼综合征中的眼眶横纹肌肉瘤
Arch Ophthalmol. 2007 Apr;125(4):566-9. doi: 10.1001/archopht.125.4.566.
7
Rhabdomyosarcoma: many similarities, a few philosophical differences.横纹肌肉瘤:诸多相似之处,些许理念差异。
J Clin Oncol. 2005 Apr 20;23(12):2586-7. doi: 10.1200/JCO.2005.11.909. Epub 2005 Feb 22.
8
[Li-Fraumeni syndrome: update, new data and guidelines for clinical management].[李-弗劳梅尼综合征:临床管理的最新进展、新数据及指南]
Bull Cancer. 2001 Jun;88(6):581-7.
9
E-cadherin germline mutations in familial gastric cancer.家族性胃癌中的E-钙黏蛋白种系突变
Nature. 1998 Mar 26;392(6674):402-5. doi: 10.1038/32918.