Rare Intronic Variants Altering Splicing Cause Lynch Syndrome: Two Case Reports

Lynch syndrome (LS) is an autosomal-dominant hereditary cancer syndrome caused by defective mismatch repair (MMR) genes. This report presents two cases of LS with rare intronic variants in MLH1 and MSH2 that affect splicing, leading to diagnostic challenges and implications for management. The first case involves a 50-year-old woman with a history of colorectal and endometrial cancers, identified with a MSH2 c.2458+976A>G variant, resulting in pseudo-exon inclusion. The second case describes a 70-year-old woman with synchronous endometrial and cecal cancers, carrying an MLH1 c.545+4_545+5del variant, which caused exon 6 skipping. Both cases have strong familial and/or medical histories of LS-related cancers, but no pathogenic variant has been detected by conventional genetic testing. In these cases, RNA sequencing played a crucial role in establishing a definitive diagnosis. These findings highlight the need for genetic testing beyond conventional exon-focused sequencing to ensure accurate diagnosis and management.

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Publication Details

Journal
Journal of obstetrics and gynaecology research
Published
2025-10-29
DOI
https://doi.org/10.1111/jog.70117
Primary Topic
Genetic factors in colorectal cancer
Type
article
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article

Rare Intronic Variants Altering Splicing Cause Lynch Syndrome: Two Case Reports

Gou Yamamoto, Tomokazu Wakatsuki, Naohiro Tomita, Kiwamu Akagi et al.
Journal of obstetrics and gynaecology research
Genetic factors in colorectal cancer
article

Rare Intronic Variants Altering Splicing Cause Lynch Syndrome: Two Case Reports

Gou Yamamoto, Tomokazu Wakatsuki, Naohiro Tomita, Kiwamu Akagi, Ikuo Matsuda, Hideaki Sawai, Hiroshi Tsubamoto, Seiji Mabuchi, Riyo Yoshii, Yumi Takimoto
article en

Abstract

Lynch syndrome (LS) is an autosomal-dominant hereditary cancer syndrome caused by defective mismatch repair (MMR) genes. This report presents two cases of LS with rare intronic variants in MLH1 and MSH2 that affect splicing, leading to diagnostic challenges and implications for management. The first case involves a 50-year-old woman with a history of colorectal and endometrial cancers, identified with a MSH2 c.2458+976A>G variant, resulting in pseudo-exon inclusion. The second case describes a 70-year-old woman with synchronous endometrial and cecal cancers, carrying an MLH1 c.545+4_545+5del variant, which caused exon 6 skipping. Both cases have strong familial and/or medical histories of LS-related cancers, but no pathogenic variant has been detected by conventional genetic testing. In these cases, RNA sequencing played a crucial role in establishing a definitive diagnosis. These findings highlight the need for genetic testing beyond conventional exon-focused sequencing to ensure accurate diagnosis and management.

Journal of obstetrics and gynaecology researchVol. 51(11)
Hyogo Medical University (JP), Toyonaka Municipal Hospital (JP), Sakai Municipal Hospital (JP), Saitama Cancer Center (JP), International University of Health and Welfare (JP), Hyogo University (JP)
Openalex Percentile: Top 56%
Genetic factors in colorectal cancer
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