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核心技术专利:CN118964589B侵权必究
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一位 48 岁的女性 MUTYH 携带者患有五种同时性原发性癌症。

Forty-eight-year-old female MUTYH carrier presenting with five concurrent primary cancers.

机构信息

Department of Surgery, University of Tennessee Medical Center, Knoxville, Tennessee, USA.

Department of Pathology, University of Tennessee Medical Center, Knoxville, Tennessee, USA.

出版信息

Cancer Rep (Hoboken). 2022 Feb;5(2):e1455. doi: 10.1002/cnr2.1455. Epub 2021 Jun 26.


DOI:10.1002/cnr2.1455
PMID:34173730
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8842692/
Abstract

BACKGROUND: MUTYH-associated polyposis is a rare disorder resulting from mutations involved in DNA mismatch repair. This results in an increased susceptibility to colonic adenomatosis and other cancers. Studies have examined the resulting frequency of extracolonic manifestations; however, these typically occur alone, concurrently, or temporally separate from an already diagnosed colorectal cancer in individuals with a biallelic mutation. CASE: Reported here is a case of five distinct primary neoplasms presenting simultaneously in a patient monoallelic for an MYH mutation. These neoplasms included squamous cell carcinoma of the vulva, rectal adenocarcinoma, synchronous anal adenocarcinoma, papillary thyroid carcinoma, and ovarian serous psammocarcinoma. Throughout her course, she underwent multiple surgical procedures, neoadjuvant chemoradiation, with further adjuvant therapy, and treatment ongoing. Due to her unique presentation, she underwent genetic testing that demonstrated she was monoallelic for an MYH mutation. CONCLUSION: The patient had a positive response to her treatment and surgical procedures with ongoing adjuvant therapy. She will continue to undergo further genetic testing, and testing for her children is being considered. This case demonstrates a unique presentation associated with a monoallelic MYH mutation that is not described in the current literature and warrants further investigation.

摘要

背景:MutYH 相关息肉病是一种罕见的疾病,由参与 DNA 错配修复的突变引起。这会导致结肠腺瘤病和其他癌症的易感性增加。已有研究检查了由此产生的结肠外表现的频率;然而,这些通常单独发生,与已诊断的结直肠癌同时发生,或在具有双等位基因突变的个体中与已诊断的结直肠癌在时间上分开。

病例报告:这里报告了一例 5 种不同的原发性肿瘤同时发生在单等位基因 MYH 突变的患者中的病例。这些肿瘤包括外阴鳞状细胞癌、直肠腺癌、同步肛门腺癌、甲状腺乳头状癌和卵巢浆液性砂粒体癌。在整个病程中,她接受了多次手术、新辅助放化疗,以及进一步的辅助治疗和正在进行的治疗。由于她的独特表现,她接受了基因检测,结果显示她的 MYH 突变是单等位基因。

结论:该患者对治疗和手术有积极反应,并正在接受辅助治疗。她将继续进行进一步的基因检测,并正在考虑对她的孩子进行检测。本病例显示了一种与单等位基因 MYH 突变相关的独特表现,目前文献中尚无描述,值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/c358445f2b93/CNR2-5-e1455-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/c96512e0bbca/CNR2-5-e1455-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/054395c62d26/CNR2-5-e1455-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/7e5b21f9425e/CNR2-5-e1455-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/4ddae9eb4ba5/CNR2-5-e1455-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/6a04ff23073c/CNR2-5-e1455-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/45825fbcc4e9/CNR2-5-e1455-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/42ac5813a0ce/CNR2-5-e1455-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/c358445f2b93/CNR2-5-e1455-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/c96512e0bbca/CNR2-5-e1455-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/054395c62d26/CNR2-5-e1455-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/7e5b21f9425e/CNR2-5-e1455-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/4ddae9eb4ba5/CNR2-5-e1455-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/6a04ff23073c/CNR2-5-e1455-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/45825fbcc4e9/CNR2-5-e1455-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/42ac5813a0ce/CNR2-5-e1455-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4027/8842692/c358445f2b93/CNR2-5-e1455-g005.jpg

相似文献

[1]
Forty-eight-year-old female MUTYH carrier presenting with five concurrent primary cancers.

Cancer Rep (Hoboken). 2022-2

[2]
Asymptomatic synchronous quintuple primary cancers.

Gynecol Obstet Invest. 2012-7-6

[3]
Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations.

Clin Genet. 2005-11

[4]
Aggressive phenotype of MYH-associated polyposis with jejunal cancer and intra-abdominal desmoid tumor: report of a case.

Dis Colon Rectum. 2009-4

[5]
Germline MUTYH (MYH) mutations in Portuguese individuals with multiple colorectal adenomas.

Hum Mutat. 2004-10

[6]
Risk of extracolonic cancers for people with biallelic and monoallelic mutations in MUTYH.

Int J Cancer. 2016-10-1

[7]
Colorectal cancer in a monoallelic MYH mutation carrier.

J Gastrointest Surg. 2013-4-27

[8]
[Multiple primary malignancies in BRCA1 mutation carriers--two clinical cases].

Ginekol Pol. 2013-10

[9]
A case report of a patient with first phenotype of papillary thyroid carcinoma and heterochronous multiprimary tumor harboring germline MUTYH Arg19*/Gly286Glu mutations.

Oral Oncol. 2021-1

[10]
Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk.

J Natl Cancer Inst. 2004-11-3

本文引用的文献

[1]
A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants.

Br J Cancer. 2010-11-9

[2]
Papillary thyroid cancer in a patient with MUTYH-associated polyposis (MAP).

Fam Cancer. 2010-12

[3]
Expanded extracolonic tumor spectrum in MUTYH-associated polyposis.

Gastroenterology. 2009-12

[4]
MUTYH-associated polyposis.

Best Pract Res Clin Gastroenterol. 2009

[5]
MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype.

Int J Cancer. 2006-8-15

[6]
Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations.

Clin Genet. 2005-11

[7]
MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps.

Gastroenterology. 2004-7

[8]
Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH.

Lancet. 2003-7-5

[9]
Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH.

N Engl J Med. 2003-2-27

[10]
Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C-->T:A mutations.

Hum Mol Genet. 2002-11-1

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