Sorbonne Université, Service de Gynécologie Obstétrique Hôpital Trousseau, AP-HP, F-75012, Faculté de Médecine Sorbonne Université, Paris, France.
Sorbonne Université, service d'Anatomie et Cytologie Pathologiques, AP-HP, Hôpital Trousseau, F-75012 Paris, France.
Eur J Obstet Gynecol Reprod Biol. 2024 Jan;292:125-132. doi: 10.1016/j.ejogrb.2023.11.024. Epub 2023 Nov 19.
MPVFD (Massive perivillous fibrin deposition) is placental lesion characterized by extensive massive deposits of fibrin in the intervillous space, extending over at least 25 % of the placental volume. Currently, this pathology can only be detected through histopathological examination of the placenta after a pregnancy has ended. The underlying mechanisms are poorly studied, there is no biomarker available for the diagnosis of MPVFD and treatment protocols are experimental and still lacking. The objective of this study is to systematically review the literature on the associated clinicopathologic features, treatment, and prognosis of MPVFD. We ended up with 17 studies, of these 12 studies were considered relevant for this article and included in the final analysis. All studies reporting MPVFD are retrospective. MPVFD is associated with recurrent miscarriage, intra uterine fetal death (IUFD), intra uterine growth restriction (IUGR) and preterm delivery. The prevalence in pregnancies with a delivery after 22 weeks of gestation was at 1.1 % and even higher to 2.7 % in recurrent early miscarriages. The reported risk of fetal death in MPVFD ranges mainly from 15 to 80 %. Preterm delivery is spontaneous in 50 to 70 % of cases and induced by of a severe intrauterine growth restriction (IUGR) in 30 to 50 % of cases depending on the study. Its causes and treatment are still poorly understood, although several avenues have been explored. This review summarizes current understanding of the prevalence, diagnostic features, clinical consequences, immune pathology, and potential prophylaxis against recurrence in this chronic inflammatory placental syndrome.
MPVFD(巨大绒毛膜下纤维蛋白沉积)是一种胎盘病变,其特征为绒毛间隙内广泛存在大量纤维蛋白沉积,至少占胎盘体积的 25%。目前,这种病理学只能通过对妊娠结束后的胎盘进行组织病理学检查来发现。其潜在机制研究不足,目前尚无用于 MPVFD 诊断的生物标志物,且治疗方案仍处于实验阶段,尚不完善。本研究旨在系统地综述 MPVFD 的相关临床病理特征、治疗和预后的文献。我们共检索到 17 项研究,其中 12 项研究与本文相关,并纳入最终分析。所有报道 MPVFD 的研究均为回顾性研究。MPVFD 与复发性流产、胎儿宫内死亡(IUFD)、宫内生长受限(IUGR)和早产有关。在 22 周后分娩的妊娠中,MPVFD 的患病率为 1.1%,而在复发性早期流产中,患病率甚至更高,为 2.7%。报道的 MPVFD 胎儿死亡风险主要在 15%至 80%之间。早产的发生率为 50%至 70%,自发性早产,30%至 50%因严重宫内生长受限(IUGR)而诱导早产,具体取决于研究。尽管已经探索了多种途径,但对其病因和治疗仍了解甚少。本综述总结了目前对这种慢性炎症性胎盘综合征的患病率、诊断特征、临床后果、免疫病理学以及潜在的复发预防的认识。