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双子宫合并双侧平滑肌瘤的复杂表现:一例报告

Complex Presentation of Uterus Didelphys With Bilateral Leiomyomas: A Case Report.

作者信息

Wube Assaye Mezgebu, Yusuf Yusuf Mohammed, Abate Biniyam Afework, Hussen Meksud Shemsu, Kebede Yabets Tesfaye, Mohammed Bekri Delil

机构信息

Department of Medicine, Ethio Tebib Hospital, Addis Ababa, Ethiopia.

Department of Medicine, Jimma University, Jimma, Ethiopia.

出版信息

Case Rep Obstet Gynecol. 2025 Jan 21;2025:6231298. doi: 10.1155/crog/6231298. eCollection 2025.

Abstract

Müllerian duct anomalies and uterine leiomyomas represent distinctive facets of female reproductive health. While uterine leiomyomas are prevalent reproductive pathologies, the coexistence of Müllerian anomalies and leiomyomas is relatively uncommon. This case study examines the complex medical and surgical management of a woman who initially presented with chronic abdominal pain and swelling. Following evaluation, the patient received a diagnosis of an uncommon co-occurrence of congenital uterus didelphys and leiomyomas. Notably, during the surgical procedure, a rectovesical peritoneal band was identified. This case study seeks to broaden the scientific understanding of these subsets of women, offering insights into the complexities arising from a common diagnosis overlaying a rare condition.

摘要

苗勒管异常和子宫平滑肌瘤是女性生殖健康的不同方面。虽然子宫平滑肌瘤是常见的生殖系统疾病,但苗勒管异常与平滑肌瘤并存的情况相对少见。本病例研究探讨了一名最初表现为慢性腹痛和腹胀的女性患者复杂的药物和手术治疗过程。经过评估,该患者被诊断为先天性双子宫与平滑肌瘤罕见并存。值得注意的是,在手术过程中发现了一条直肠膀胱腹膜带。本病例研究旨在拓宽对这些女性亚群的科学认识,深入了解罕见病症叠加常见诊断所产生的复杂性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3b8/11774576/50b2d3e0afee/CRIOG2025-6231298.001.jpg

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