Chronic sterile inflammation in the pathogenesis of benign myometrial diseases
Chronic sterile inflammation, marked by DAMPs, underlies the pathogenesis of adenomyosis and uterine fibroids through shared mechanisms involving abnormal cell division, neoangiogenesis, neoneurogenesis, and fibrosis.
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This review analyzes existing literature to establish chronic sterile inflammation as a central mechanism in the pathogenesis of benign myometrial diseases, specifically adenomyosis and uterine fibroids. The authors identify damage-associated molecular patterns (DAMPs) as key markers of inflammation severity that drive neoangiogenesis, neoneurogenesis, and fibrosis through abnormal cell division responses. Genetic and epigenetic factors determine whether these inflammatory processes manifest as fibroids or adenomyosis, leading to clinical symptoms such as pain, bleeding, and infertility. The paper concludes by recommending further investigation into the systemic immune profile and cellular composition of these tissues to clarify the role of inflammation. This paper is centrally about adenomyosis — it examines its pathogenesis alongside uterine fibroids through the lens of chronic sterile inflammation.
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