儿童横纹肌肉瘤：流行病学研究及一种家族性癌症综合征的鉴定 - Suppr

Suppr

超能文献

Rhabdomyosarcoma in children: epidemiologic study and identification of a familial cancer syndrome.

作者信息

Li F P, Fraumeni J F

出版信息

J Natl Cancer Inst. 1969 Dec;43(6):1365-73.

PMID:5396222

Abstract

摘要

相似文献

Rhabdomyosarcoma in children: epidemiologic study and identification of a familial cancer syndrome.儿童横纹肌肉瘤：流行病学研究及一种家族性癌症综合征的鉴定

J Natl Cancer Inst. 1969 Dec;43(6):1365-73.

Heredity and cancer in man.人类的遗传与癌症。

Prog Med Genet. 1973;9:113-58.

[Familial cancer. 2. The S.B.L.A. syndrome: sarcoma of the breast, brain, leukemia and adrenals].[家族性癌症。2. S.B.L.A. 综合征：乳腺癌、脑癌、白血病和肾上腺肉瘤]

Union Med Can. 1985 Jun;114(6):476-80.

Mucosal neuroma syndrome. Syndrome of bilateral pheochromocytoma, medullary thyroid carcinoma, and multiple neuromas.黏膜神经瘤综合征。双侧嗜铬细胞瘤、甲状腺髓样癌和多发性神经瘤综合征。

Am J Dis Child. 1971 Mar;121(3):235-6.

Association of soft tissue sarcoma, leukemia, and brain tumors in families affected with breast cancer.

Am Surg. 1973 Apr;39(4):199-206.

Genetic factors in breast cancer: a survey.乳腺癌中的遗传因素：一项调查。

Pathol Annu. 1976;11:77-101.

The cancer family syndrome and cancer control.癌症家族综合征与癌症控制。

Surg Gynecol Obstet. 1971 Feb;132(2):247-50.

The sarcoma, breast cancer, lung cancer, and adrenocortical carcinoma syndrome revisited. Childhood cancer.肉瘤、乳腺癌、肺癌和肾上腺皮质癌综合征再探讨。儿童癌症。

Am J Dis Child. 1985 Feb;139(2):134-6. doi: 10.1001/archpedi.1985.02140040032020.

BRCA2: a cause of Li-Fraumeni-like syndrome.BRCA2：一种李-佛美尼样综合征的病因。

J Med Genet. 2008 Jan;45(1):62-3. doi: 10.1136/jmg.2007.054494.

Multiple endocrine neoplasia, type II: a combined surgical and genetic approach to treatment.II型多发性内分泌腺瘤病：一种手术与基因相结合的治疗方法。

Can Med Assoc J. 1981 Feb 15;124(4):403-10.

引用本文的文献

TP53 variant clusters stratify phenotypic diversity in germline carriers and reveal an osteosarcoma-prone subgroup.TP53变异簇对种系携带者的表型多样性进行分层，并揭示了一个易患骨肉瘤的亚组。

Nat Commun. 2025 Sep 29;16(1):8546. doi: 10.1038/s41467-025-63528-6.

Li-Fraumeni Syndrome : Current Strategies and Future Perspectives.李-佛美尼综合征：当前策略与未来展望

J Korean Neurosurg Soc. 2025 May;68(3):305-310. doi: 10.3340/jkns.2025.0050. Epub 2025 Apr 29.

Exploiting somatic oncogenic driver alterations in a patient with Li-Fraumeni syndrome- paving the path towards precision medicine: a case report.利用李-弗劳梅尼综合征患者的体细胞致癌驱动基因改变——迈向精准医学之路：一例病例报告

J Cancer Res Clin Oncol. 2025 Jan 16;151(1):37. doi: 10.1007/s00432-024-06077-7.

Mutant p53 reactivation restricts the protumorigenic consequences of wild type p53 loss of heterozygosity in Li-Fraumeni syndrome patient-derived fibroblasts.突变型 p53 的重新激活限制了 Li-Fraumeni 综合征患者来源成纤维细胞中野生型 p53 杂合性丢失的促肿瘤发生后果。

Cell Death Differ. 2024 Jul;31(7):855-867. doi: 10.1038/s41418-024-01307-4. Epub 2024 May 14.

Cancer Risks Associated With Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum.与致病性变异相关的癌症风险：Li-Fraumeni 综合征谱之外的首发癌症的扩展家系的最大似然分析。

JCO Precis Oncol. 2024 Feb;8:e2300453. doi: 10.1200/PO.23.00453.

Malignant and Benign Head and Neck Tumors of the Pediatric Age: A Narrative Review.儿童期头颈部良恶性肿瘤：一项叙述性综述

Curr Pediatr Rev. 2025;21(2):118-132. doi: 10.2174/0115733963258575231123043807.

Epithelioid angiomyolipoma of the liver in a patient with Li-Fraumeni syndrome: a case report.肝脏上皮样血管平滑肌脂肪瘤合并 Li-Fraumeni 综合征 1 例报告

Diagn Pathol. 2024 Jan 19;19(1):16. doi: 10.1186/s13000-023-01418-5.

Lessons learnt from the clinico-genomic profiling of families with Li Fraumeni syndrome at a tertiary care centre in North India.从印度北部一家三级医疗中心对李-佛美尼综合征家族进行的临床基因组分析中吸取的经验教训。

Ecancermedicalscience. 2023 May 11;17:1550. doi: 10.3332/ecancer.2023.1550. eCollection 2023.

TP53 germline pathogenic variant frequency in anaplastic rhabdomyosarcoma: A Children's Oncology Group report.间变性横纹肌肉瘤中TP53种系致病变异频率：儿童肿瘤学组报告

Pediatr Blood Cancer. 2023 May 17:e30413. doi: 10.1002/pbc.30413.

Genomic profile of two Brazilian choroid plexus tumors by whole-exome sequencing.巴西两个脉络丛肿瘤的全外显子组测序基因组分析。

Cold Spring Harb Mol Case Stud. 2023 Mar 24;9(1). doi: 10.1101/mcs.a006245. Print 2023 Feb.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验