ArticleRadiology case reports2026
Retrograde menses presented as acute stump appendicitis- Mayer-Rokitansky-Küster-Hauser syndrome.
Article in Radiology case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is an exceptionally rare condition. This article highlights its unusual presentation and the role of radiological imaging in the diagnosis and outlines an approach to management. A 17-year-old female presented to the hospital with symptoms typical of acute appendicitis. However, further evaluation revealed no menstrual bleeding, recurrent monthly abdominal pain, and the absence of a uterus on imaging. These findings raised suspicion for Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. The presentation mimicking acute appendicitis in this context is an exceptionally rare occurrence. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare condition that presents a considerable challenge in terms of diagnosis and management. A thorough clinical history, along with appropriate imaging and investigations, is essential for the timely identification of the syndrome and for guiding effective management.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.