Imaging of leiomyomas arising from Müllerian remnants in a case of Mayer-Rokitansky-Küster-Hauser syndrome
article
OA: bronze
CC0
⤵ 2 in-corpus citations
AI-generated summary
This case report details a 43-year-old woman with Mayer-Rokitansky-Küster-Hauser syndrome who was found to have multiple large leiomyomas arising from Müllerian remnant tissue on MRI.
One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works
Abstract
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare congenital abnormality characterised by varying degrees of aplasia or hypoplasia of the uterus and vagina. Very rarely, leiomyomas or adenomyosis can develop in the Müllerian remnant tissue or rudimentary uterus. We present a case of a 43-year-old woman with MRKH syndrome, who presented with primary amenorrhoea and lower abdominal pain. On examination, a large pelvic mass was palpated and a provisional diagnosis of ovarian tumour was made. MRI showed multiple large leiomyomas arising from the Müllerian remnant tissue, and chronic torsion of the right ovary.
My notes (saved in your browser only)
Condition tags
MeSH descriptors
Citation neighborhood (sparse)
Too few in-corpus citations on either side for a chart; here are the lists.
Cites (1)
Cited by (2)
References (4)
- Rare case of leiomyoma in Mayer-Rokitansky-Kuster-Hauser syndrome via openalex
- W2060438950 via openalex
- W2086417042 via openalex
- W2099353796 via openalex
Cited by (2)
Source provenance
- europepmc
- last seen: 2026-06-17T06:13:18.893374+00:00
- openalex
- last seen: 2026-06-04T00:00:01.174412+00:00
- pubmed
- last seen: 2026-05-13T22:17:39.907309+00:00
License: CC0
· commercial use OK