Department of Surgery, University of Tennessee Medical Center, Knoxville, Tennessee, USA.
Department of Pathology, University of Tennessee Medical Center, Knoxville, Tennessee, USA.
Cancer Rep (Hoboken). 2022 Feb;5(2):e1455. doi: 10.1002/cnr2.1455. Epub 2021 Jun 26.
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.
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。
Cancer Rep (Hoboken). 2022-2
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