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胎盘间充质发育不良:与中期胎儿生长受限相关的罕见病例。

Placental mesenchymal dysplasia: a rare case associated with second trimester fetal growth restriction.

机构信息

Obstetrics & Gynecology department, Whiston Hospital, Prescot, L35 5DR, UK.

出版信息

BMC Pregnancy Childbirth. 2024 Nov 25;24(1):786. doi: 10.1186/s12884-024-06960-8.

DOI:10.1186/s12884-024-06960-8
PMID:39587496
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11587632/
Abstract

BACKGROUND

Placental mesenchymal dysplasia (PMD) is a rare, benign, placental disorder characterised macroscopically by an enlarged multi-cystic placenta. It is a condition associated with a range of reported clinical outcomes and can be misdiagnosed as a molar or partial molar pregnancy given the similarities in clinical presentation. We present an unusual case of PMD complicated by fetal growth restriction and oligohydramnios in the second trimester.

CASE PRESENTATION

A 33 year old female was referred to our fetal medicine unit with a multi-cystic placenta at dating scan suspected initially to be a partial molar pregnancy. She opted for conservative management and declined invasive testing. At 16 weeks severe fetal growth restriction was present with an estimated fetal weight < 3rd centile and associated with oligohydramnios. Whilst live births in cases of PMD have been reported in the literature, to our knowledge there are no reported successful outcomes in cases of early onset growth restriction at this gestation. The patient opted to proceed with termination of pregnancy given the suspected poor prognosis. Post mortem results confirmed a diagnosis of PMD and fetal growth restriction with normal genetic testing.

CONCLUSIONS

Placental mesenchymal dysplasia can be a difficult condition to manage, particularly when counselling about prognosis and deciding whether to continue the pregnancy. More evidence is needed about prognostic factors in PMD associated with a successful outcome. Early onset fetal growth restriction and/or oligohydramnios prior to 20 weeks are likely poor prognostic factors which should be considered in the antenatal counselling.

摘要

背景

胎盘间质发育不良(PMD)是一种罕见的良性胎盘疾病,其宏观特征为多房性胎盘增大。由于临床表现相似,它是一种与多种报道的临床结局相关的疾病,可能被误诊为葡萄胎或部分葡萄胎。我们报告了一例罕见的 PMD 病例,在妊娠中期并发胎儿生长受限和羊水过少。

病例介绍

一名 33 岁女性因在孕早期的超声检查中发现多房性胎盘,疑似部分葡萄胎,被转诊至我们的胎儿医学科。她选择了保守治疗并拒绝了有创性检查。在 16 周时,出现严重的胎儿生长受限,估计胎儿体重<第 3 百分位数,伴有羊水过少。尽管文献中有 PMD 病例活产的报道,但据我们所知,在这个孕龄出现早期生长受限的病例中,尚无成功结局的报道。鉴于可疑的不良预后,患者选择终止妊娠。尸检结果证实了 PMD 和胎儿生长受限的诊断,遗传检测正常。

结论

PMD 的管理较为困难,尤其是在预后咨询和决定是否继续妊娠时。需要更多关于 PMD 相关成功结局的预后因素的证据。20 周前出现的早期胎儿生长受限和/或羊水过少可能是不良预后因素,在产前咨询中应予以考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d603/11587632/d5062b002f46/12884_2024_6960_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d603/11587632/a7eea7a34b34/12884_2024_6960_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d603/11587632/c86dde0a53ee/12884_2024_6960_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d603/11587632/d5062b002f46/12884_2024_6960_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d603/11587632/a7eea7a34b34/12884_2024_6960_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d603/11587632/c86dde0a53ee/12884_2024_6960_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d603/11587632/d5062b002f46/12884_2024_6960_Fig4_HTML.jpg

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