Guo Sun-Wei
Shanghai Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
Shanghai Key Laboratory of Female Reproductive Endocrine-Related Diseases, Fudan University, Shanghai, China.
Reproduction. 2022 Oct 10;164(5):R101-R121. doi: 10.1530/REP-22-0224. Print 2022 Nov 1.
Traditionally viewed as enigmatic and elusive, adenomyosis is a fairly common gynecological disease but is under-recognized and under-researched. This review summarizes the latest development on the pathogenesis and pathophysiology of adenomyosis, which have important implications for imaging diagnosis of the disease and for the development of non-hormonal therapeutics.
Traditionally considered as an enigmatic disease, adenomyosis is a uterine disease that affects many women of reproductive age and is a contributing factor for pelvic pain, heavy menstrual bleeding (HMB), and subfertility. In this review, the new development in the pathogenesis and pathophysiology of adenomyosis has been summarized, along with their clinical implications. After reviewing the progress in our understanding of the pathogenesis and describing the prevailing theories, in conjunction with their deficiencies, a new hypothesis, called endometrial-myometrial interface disruption (EMID), which is backed by extensive epidemiologic data and demonstrated by a mouse model, is reviewed, along with recent data implicating the role of Schwann cells in the EMI area in the genesis of adenomyosis. Additionally, the natural history of adenomyotic lesions is elaborated and underscores that, in essence, adenomyotic lesions are fundamentally wounds undergoing repeated tissue injury and repair (ReTIAR), which progress to fibrosis through epithelial-mesenchymal transition, fibroblast-to-myofibroblast transdifferentiation, and smooth muscle metaplasia. Increasing lesional fibrosis propagates into the neighboring EMI and endometrium. The increased endometrial fibrosis, with ensuing greater tissue stiffness, results in attenuated prostaglandin E2, hypoxia signaling and glycolysis, impairing endometrial repair and causing HMB. Compared with adenomyosis-associated HMB, the mechanisms underlying adenomyosis-associated pain are less understood but presumably involve increased uterine contractility, hyperinnervation, increased lesional production of pain mediators, and central sensitization. Viewed through the prism of ReTIAR, a new imaging technique can be used to diagnose adenomyosis more accurately and informatively and possibly help to choose the best treatment modality.
子宫腺肌病传统上被视为神秘且难以捉摸,它是一种相当常见的妇科疾病,但却未得到充分认识和研究。本综述总结了子宫腺肌病发病机制和病理生理学的最新进展,这些进展对该疾病的影像学诊断以及非激素治疗的发展具有重要意义。
子宫腺肌病传统上被认为是一种神秘的疾病,它是一种影响许多育龄妇女的子宫疾病,是盆腔疼痛、月经过多(HMB)和生育力低下的一个促成因素。在本综述中,总结了子宫腺肌病发病机制和病理生理学的新进展及其临床意义。在回顾了我们对发病机制的理解进展并描述了主流理论及其不足之处后,一种新的假说,即子宫内膜 - 肌层界面破坏(EMID),得到了广泛的流行病学数据支持并在小鼠模型中得到证实,同时还回顾了近期涉及雪旺细胞在子宫腺肌病发生中在EMI区域作用的数据。此外,阐述了子宫腺肌病病变的自然史,并强调子宫腺肌病病变本质上是经历反复组织损伤和修复(ReTIAR)的基本伤口,通过上皮 - 间充质转化、成纤维细胞向肌成纤维细胞转分化和平滑肌化生进展为纤维化。病变纤维化的增加扩散到邻近的EMI和子宫内膜。子宫内膜纤维化增加,随之组织硬度增加,导致前列腺素E2、缺氧信号和糖酵解减弱,损害子宫内膜修复并导致月经过多。与子宫腺肌病相关的月经过多相比,子宫腺肌病相关疼痛的潜在机制了解较少,但可能涉及子宫收缩力增加、神经支配过度、病变疼痛介质产生增加和中枢敏化。从ReTIAR的角度来看,一种新的成像技术可用于更准确、更有信息地诊断子宫腺肌病,并可能有助于选择最佳治疗方式。