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罕见型赫尔林-韦纳-武德连综合征中成功的早产妊娠:病例报告。

Successful preterm pregnancy in a rare variation of Herlyn-Werner-Wunderlich syndrome: a case report.

机构信息

Department of Biomedicine and Prevention, Obstetrics and Gynecological Clinic, University of Rome "Tor Vergata", via Montpellier 1, 00133, Rome, Italy.

Department of Woman's and Child's Health, Obstetrics and Gynecological Unit, San Camillo-Forlanini Hospital, Circonvallazione Gianicolense 87, 00152, Rome, Italy.

出版信息

BMC Pregnancy Childbirth. 2018 Dec 17;18(1):498. doi: 10.1186/s12884-018-2133-2.

Abstract

BACKGROUND

Herlyn-Werner-Wunderlich syndrome (HWWS) is an uncommon congenital anomaly of the female urogenital tract, characterised by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. We reported the difficult pregnancy course complicated by an extremely rare and unique case of this syndrome associated with ectrodactyly, a clinical combination never described in literature.

CASE PRESENTATION

A 28- year-old nulliparous woman previously diagnosed for HWWS associated with ectrodactyly of the right foot and with a history of abdominal left hemi-hysterectomy, ipsilateral salpingectomy, vaginal reconstruction when she was an adolescent. She suffered from threats of abortion in the first trimester, recurrent urinary tract infections during all pregnancy. At 33 weeks + 5 days of gestational age, she was hospitalized for premature rupture of the membranes and uterine contractions and a caesarean section was performed because of breech presentation. Postpartum period was complicated by a pelvic abscess resolved with parental antibiotic therapies.

CONCLUSIONS

Our literature review shows an unusual aspect in our case: HWWS is not classically associated with skeletal anomalies. Moreover, the most frequent urogenital side affected is the right, not left side as in this woman. Preterm spontaneous rupture of membranes and fetal abnormal presentation represent frequent complications and probably post-caesarean infections are related to pregnancies in the context of this syndrome.

摘要

背景

赫尔林-韦纳-武德希(HWWS)综合征是一种罕见的女性生殖道先天性异常,其特征为双子宫、阴道半阻塞和同侧肾发育不全。我们报告了一例妊娠过程复杂的罕见病例,该病例与独特的外胚层发育不良有关,这种临床组合在文献中从未描述过。

病例介绍

一名 28 岁的初产妇,曾被诊断为 HWWS 合并右足并指畸形,并于青少年时期行左侧半子宫切除术、同侧输卵管切除术和阴道重建术。她在妊娠早期经历了流产威胁,整个妊娠期间反复发生尿路感染。在妊娠 33 周+5 天时,因胎膜早破和子宫收缩住院,并因臀位行剖宫产术。产后期间并发骨盆脓肿,经父母抗生素治疗后痊愈。

结论

我们的文献回顾显示了我们病例的一个不寻常方面:HWWS 不常与骨骼异常相关。此外,受影响最常见的泌尿生殖侧为右侧,而不是本例中的左侧。自发性胎膜早破和胎儿异常表现是常见的并发症,剖宫产术后感染可能与该综合征相关的妊娠有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fd1/6296152/bd4872a8215d/12884_2018_2133_Fig1_HTML.jpg

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