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苗勒管异常与子宫内膜异位症:关联及表型变异

Müllerian anomalies and endometriosis: associations and phenotypic variations.

作者信息

Bhamidipaty-Pelosi Surya, Kyei-Barffour Isaac, Volpert Marianna, O'Neill Nora, Grimshaw Alyssa, Eriksson Lars, Vash-Margita Alla, Pelosi Emanuele

机构信息

Department of Clinical Pharmacology, Indiana University School of Medicine, Indianapolis, IN, USA.

Royal Brisbane and Women's Hospital, The University of Queensland, Brisbane, QLD, Australia.

出版信息

Reprod Biol Endocrinol. 2024 Dec 19;22(1):157. doi: 10.1186/s12958-024-01336-1.

Abstract

Müllerian anomalies are congenital conditions characterized by the incomplete development of the female reproductive tract. Women affected by Müllerian anomalies often display additional malformations of the renal, skeletal, and cardiovascular system, and are at a higher risk for infertility and adverse pregnancy outcomes. Several Müllerian anomalies have been reported in association with endometriosis, but it is unclear if all classes or anatomical variations are associated with the disease. Most importantly, both Müllerian anomalies and endometriosis can manifest with a wide degree of variability, adding further complexity to their poorly defined relationship. Retrograde menstruation occurring in obstructive Müllerian anomalies is a well-accepted mechanism for the development of endometriosis. However, endometriosis can occur following surgical correction of the anomaly or in the absence of obstruction. This suggests that other mechanisms may be involved, although the specific pathogenesis remains elusive. This review provides a comprehensive summary of the current state of clinical research on endometriosis in Müllerian anomalies. This review also highlights research and knowledge gaps, informing the development of future experimental designs to address current limitations including heterogeneity of phenotypes, variable comorbidities, and lack of genetic information.

摘要

苗勒管异常是一种先天性疾病,其特征为女性生殖道发育不完全。受苗勒管异常影响的女性常伴有肾脏、骨骼和心血管系统的其他畸形,并且不孕和不良妊娠结局的风险更高。已有多种苗勒管异常与子宫内膜异位症相关的报道,但尚不清楚所有类型或解剖变异是否均与该疾病相关。最重要的是,苗勒管异常和子宫内膜异位症均可表现出广泛的变异性,这使得它们之间关系的界定更加复杂。梗阻性苗勒管异常中发生的经血逆流是子宫内膜异位症发病的一个公认机制。然而,在对异常进行手术矫正后或在无梗阻的情况下也可发生子宫内膜异位症。这表明可能涉及其他机制,尽管具体发病机制仍不清楚。本综述全面总结了苗勒管异常中子宫内膜异位症的临床研究现状。本综述还强调了研究和知识空白,为未来实验设计的开展提供信息,以解决当前的局限性,包括表型异质性、可变的合并症和缺乏遗传信息等问题。

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