ArticleCureus2026
Unicornuate Uterus With a Rudimentary Horn Adenomyoma, Ipsilateral Renal Agenesis, and Deep Infiltrating Endometriosis: A Case Report.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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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.
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Authors and funding
4 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Congenital uterine malformations are often difficult to classify, and an incorrect label can carry over for years across successive clinical records. We describe a 39-year-old woman, gravida 1 para 1, referred for chronic pelvic pain and intermenstrual bleeding, whose uterus had previously been recorded as didelphys. Pelvic magnetic resonance imaging, with T2-weighted sequences in three planes, T1-weighted and fat-saturated sequences, diffusion-weighted imaging, and post-gadolinium imaging, instead demonstrated a unicornuate uterus with a left, cavitated, non-communicating functional rudimentary horn (European Society of Human Reproduction and Embryology/European Society for Gynaecological Endoscopy (ESHRE/ESGE) class U4a; American Society for Reproductive Medicine (ASRM) unicornuate uterus with a non-communicating rudimentary horn). The rudimentary horn was almost entirely occupied by a 6 cm adenomyoma, with a small residual endometrial-lined cavity; the contralateral functional horn showed diffuse adenomyosis; a deep infiltrating endometriotic nodule extended to the left pelvic sidewall with neurovascular tethering and rectal tenting but no transmural invasion; the left ovary contained an endometrioma; and the left kidney was absent. Surgery and histopathology confirmed a single cervix with a rudimentary horn fused at the cervical level, together with the adenomyoma, extensive adenomyosis, and ovarian endometriosis; the patient recovered without complications and became asymptomatic. The case shows how imaging settled a long-standing classification error and how a single examination characterized the associated renal and endometriotic findings that follow from the shared embryology of the genital and urinary tracts.
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