# Elevated Risk of Endometrial Cancer and Precursor Lesions in Patients With Myotonic Dystrophy: A Retrospective Study at a Single Institution in Japan

**Authors:** Ruka Hano, Hirofumi Ando, Marina Fujioka, Masako Nakajima, Manaka Shinagawa, Hodaka Takeuchi, Mitsuko Shinagawa, Hisanori Kobara, Tsuneaki Yoshinaga, Tsutomu Miyamoto

PMC · DOI: 10.1111/jog.70221 · The Journal of Obstetrics and Gynaecology Research · 2026-02-26

## TL;DR

This study found that Japanese women with myotonic dystrophy have a higher risk of endometrial cancer and related conditions at a younger age compared to others.

## Contribution

The study provides new evidence on elevated endometrial cancer risk in Japanese myotonic dystrophy patients.

## Key findings

- 13.9% of Japanese MD patients had endometrial cancer or precursor lesions compared to 1.2% in controls.
- MD patients were diagnosed at a median age of 45, significantly younger than non-MD cases.
- All surgically treated MD-related endometrial cancers were early-stage with good outcomes.

## Abstract

Myotonic dystrophy (MD) has been associated with an increased risk of endometrial cancer (EC) in Western countries; however, data from Japan are limited. This study aimed to evaluate the incidence and clinical characteristics of EC and its precursor lesion, atypical endometrial hyperplasia (AEH), in Japanese patients with MD.

We retrospectively reviewed medical records of female patients with MD (MD group, n = 36) and those with other types of muscular dystrophy (control group, n = 84) treated at a single institution between 2008 and 2023.

EC/AEH was identified in 5 of 36 patients in the MD group (13.9%), including 3 cases of EC and 2 of AEH, whereas 1 case of EC (1.2%) was observed among 84 control patients, indicating a significantly higher incidence in the MD group (p = 0.014). The median age at diagnosis of EC/AEH in the MD group was 45 years, which was significantly younger than that of non‐MD EC/AEH cases treated during the same period (median 59 years). All surgically treated EC cases were early‐stage endometrioid carcinoma and achieved favorable oncological outcomes, although perioperative respiratory complications were observed.

Japanese MD patients have a significantly higher risk of developing EC/AEH at a younger age compared with non‐MD patients. These findings highlight the importance of regular gynecological surveillance in women with MD.

## Linked entities

- **Diseases:** Myotonic dystrophy (MONDO:0016107), Endometrial cancer (MONDO:0002447), Atypical endometrial hyperplasia (MONDO:0006096)

## Full-text entities

- **Genes:** CASP5 (caspase 5) [NCBI Gene 838] {aka ICE(rel)III, ICEREL-III, ICH-3}, PDK4 (pyruvate dehydrogenase kinase 4) [NCBI Gene 5166], DAPK1 (death associated protein kinase 1) [NCBI Gene 1612] {aka DAPK, ROCO3}, DMPK (DM1 protein kinase) [NCBI Gene 1760] {aka DM, DM1, DM1PK, DMK, MDPK, MT-PK}, CNBP (CCHC-type zinc finger nucleic acid binding protein) [NCBI Gene 7555] {aka CNBP1, DM2, PROMM, RNF163, ZCCHC22, ZNF9}, PLA2G7 (phospholipase A2 group VII) [NCBI Gene 7941] {aka LDL-PLA2, LP-PLA2, PAFAD, PAFAH}, CEBPD (CCAAT enhancer binding protein delta) [NCBI Gene 1052] {aka C/EBP-delta, CELF, CRP3, NF-IL6-beta}, INSR (insulin receptor) [NCBI Gene 3643] {aka CD220, HHF5}, MBNL1 (muscleblind like splicing regulator 1) [NCBI Gene 4154] {aka EXP, MBNL}
- **Diseases:** tumor suppressor microRNA family 200c/141 (OMIM:601308), insulin resistance (MESH:D007333), infertility (MESH:D007246), pneumothorax (MESH:D011030), colorectal cancer (MESH:D015179), myotonia (MESH:D009222), thyroid cancer (MESH:D013964), tumorigenic (MESH:D002471), precancerous lesion (MESH:D011230), EC (MESH:D016889), cardiac conduction defects (MESH:D000075224), Types of muscular dystrophy (MESH:D009136), ovarian cancer (MESH:D010051), cardiac conditions (MESH:D006331), respiratory muscle dysfunction (MESH:D009135), AEH (MESH:D004714), abnormal genital bleeding (MESH:D014564), cataracts (MESH:D002386), DM1 (MESH:D009223), cervical intraepithelial neoplasia (MESH:D002578), muscle weakness (MESH:D018908), diabetes mellitus (MESH:D003920), endometrioid carcinoma (MESH:D018269), benign tumors (MESH:D009369), thyroid nodules (MESH:D016606), respiratory infections (MESH:D012141), hypoxemia (MESH:D000860), hypothalamic amenorrhea (MESH:D000568), Becker muscular dystrophy (MESH:D020388), autosomal dominant disorder (MESH:D030342), overweight (MESH:D050177), carcinogenesis (MESH:D063646), testicular cancer (MESH:D013736), cardiac conduction abnormalities (MESH:D006327), arrhythmia (MESH:D001145), limb-girdle muscular dystrophy (MESH:D049288), skin tumors (MESH:D012878), obesity (MESH:D009765), colorectal polyps (MESH:D003111), Restrictive ventilatory impairment (MESH:D012131)
- **Chemicals:** oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC12939248/full.md

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Source: https://tomesphere.com/paper/PMC12939248