Mayer-Rokitansky-Küster-Hauser Syndrome With Concurrent Adenomyosis and Leiomyoma in Rudimentary Uterus: A Case Report

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AI-generated summary by claude@2026-06, 2026-06-23

This case report details a 35-year-old woman with MRKH syndrome found to have adenomyosis and a leiomyoma in uterine remnants, highlighting the need for careful imaging in MRKH patients.

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AI-generated deep summary by claude@2026-06, 2026-06-10 · read from full text

This paper reports a rare case of Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome in a 35-year-old woman who presented with progressive lower abdominal pain and was evaluated with diagnostic imaging. Initial ultrasound suggested an adnexal mass, but subsequent imaging identified bilateral rudimentary uterine remnants, including one with adenomyotic changes and the other containing a leiomyoma, which was confirmed by laparoscopic excision. A stated limitation is that the work is a single case report, which does not establish broader prevalence or generalizable causal mechanisms. This paper is centrally about adenomyosis within a Müllerian remnant context in MRKH, and it directly documents concurrent adenomyosis and leiomyoma in rudimentary uterus.

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Abstract

We report a rare case of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome accompanied by simultaneous adenomyosis and leiomyoma in rudimentary uterine remnants. A 35-year-old woman presented with progressive lower abdominal pain and underwent diagnostic imaging. The initial ultrasound erroneously suggested an adnexal mass, but subsequent imaging revealed bilateral uterine remnants-one with adenomyotic changes and the other harboring a leiomyoma. Laparoscopic excision confirmed these pathological findings. This case suggests the importance of regular gynecological imaging examinations for MRKH patients and challenges the conventional belief in the non-functional nature of Müllerian remnants. Furthermore, our findings underscore the diagnostic utility of transabdominal ultrasound in accurately identifying complex uterine anomalies.
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Mayer–Rokitansky–Küster–Hauser Syndrome With Concurrent Adenomyosis and Leiomyoma in Rudimentary Uterus: A Case Report Funding: This work was supported by the National Health Commission of the People's Republic of China (IHECC-2022C20004). ABSTRACT We report a rare case of Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome accompanied by simultaneous adenomyosis and leiomyoma in rudimentary uterine remnants. A 35-year-old woman presented with progressive lower abdominal pain and underwent diagnostic imaging. The initial ultrasound erroneously suggested an adnexal mass, but subsequent imaging revealed bilateral uterine remnants—one with adenomyotic changes and the other harboring a leiomyoma. Laparoscopic excision confirmed these pathological findings. This case suggests the importance of regular gynecological imaging examinations for MRKH patients and challenges the conventional belief in the non-functional nature of Müllerian remnants. Furthermore, our findings underscore the diagnostic utility of transabdominal ultrasound in accurately identifying complex uterine anomalies. Conflicts of Interest The authors declare no conflicts of interest. Data Availability Statement The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.

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Condition tags

adenomyosis

MeSH descriptors

46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development 46, XX Disorders of Sex Development

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Source provenance

europepmc
last seen: 2026-08-07T06:07:27.085738+00:00
pubmed
last seen: 2026-08-07T06:03:53.109537+00:00
unpaywall
last seen: 2026-05-11T08:34:28.763810+00:00
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