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一种罕见的先天性会阴沟。

A Rare Congenital Perineal Groove.

作者信息

Abate Enyew

机构信息

Department of Obstetrics and Gynecology, College of Medicine and Health Sciences, Bahir dar University, Ethiopia.

出版信息

Case Rep Obstet Gynecol. 2022 Oct 27;2022:8797205. doi: 10.1155/2022/8797205. eCollection 2022.

DOI:10.1155/2022/8797205
PMID:36338543
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9633183/
Abstract

BACKGROUND

Perineal groove is a rare congenital anomaly characterized by nonepithelialized mucous membrane that appears as an erythematous sulcus in the perineal midline, extending from the posterior vaginal fourchette to the anterior anal orifice. It is one of the uncommon anomalies of anogenital region that is unknown to many clinicians, and it is usually misdiagnosed as an anal fissure, perineal trauma, diaper dermatitis, infection, or sexual abuse. . Seven-day-old female neonate was brought by her parents after they observe reddish discoloration of her genitalia. Upon examination, there was a vertical perineal wet groove-like unkeratinized erythematous lesion with no bleeding, sign of infection, or inflammation that extends from the posterior vaginal fourchette to the anal rim. The newborn was sent home after counseling with a reassessment plan in case of complications.

CONCLUSIONS

Recognition of the congenital perineal groove at birth is important for the health care providers to deliver an appropriate parental counseling and appropriate follow-up.

摘要

背景

会阴沟是一种罕见的先天性异常,其特征为无上皮化的黏膜,表现为会阴中线处的一条红斑性沟,从阴道后穹延伸至肛门开口前部。它是许多临床医生不了解的肛门生殖器区域不常见的异常之一,通常被误诊为肛裂、会阴创伤、尿布皮炎、感染或性虐待。一名7日龄女新生儿在其父母观察到其生殖器发红后被带来就诊。检查时,发现有一条垂直的会阴湿沟样未角化的红斑性病变,无出血、感染迹象或炎症,从阴道后穹延伸至肛门边缘。在给予咨询并制定并发症再评估计划后,该新生儿被送回家。

结论

出生时识别先天性会阴沟对于医护人员进行适当的家长咨询和适当的随访很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73ff/9633183/633d5d67e6cf/CRIOG2022-8797205.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73ff/9633183/633d5d67e6cf/CRIOG2022-8797205.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73ff/9633183/633d5d67e6cf/CRIOG2022-8797205.001.jpg

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本文引用的文献

1
Perineal Groove: Is It More Common Than We Think? Clinical Characteristics of Four Cases and Review of Literature.会阴沟:是否比我们想象的更常见?4例临床特征及文献复习
Pediatr Rep. 2021 Aug 9;13(3):490-494. doi: 10.3390/pediatric13030056.
2
Congenital Perineal Groove Defect in Monozygotic Twin Infants: A Literature Review.单卵双胎婴儿先天性会阴沟缺陷:文献综述
AJP Rep. 2021 Jan;11(1):e54-e57. doi: 10.1055/s-0041-1727145. Epub 2021 Mar 31.
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Perineal Groove: An Anorectal Malformation Network, Consortium Study.会阴沟:肛门直肠畸形网络,联合会研究。
J Pediatr. 2020 Jul;222:207-212. doi: 10.1016/j.jpeds.2020.03.026.
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Four Cases of Perineal Groove-Experience of a Greek Maternity Hospital.会阴沟四例——希腊一家妇产医院的经验。
Medicina (Kaunas). 2019 Aug 15;55(8):488. doi: 10.3390/medicina55080488.
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Perineal Groove: Report of Two Cases and Review of the Literature.会阴沟:两例报告及文献综述
Front Pediatr. 2018 Aug 15;6:227. doi: 10.3389/fped.2018.00227. eCollection 2018.
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Congenital perineal groove.先天性会阴沟
Arch Dis Child. 2019 Mar;104(3):286. doi: 10.1136/archdischild-2017-314554. Epub 2018 Feb 7.
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Perineal groove in female infants: A case series and literature review.
Pediatr Dermatol. 2017 Nov;34(6):677-680. doi: 10.1111/pde.13311. Epub 2017 Oct 11.
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Perineal Groove: A Rare Congenital Midline Defect of Perineum.会阴沟:一种罕见的先天性会阴中线缺损。
AJP Rep. 2016 Mar;6(1):e30-2. doi: 10.1055/s-0035-1566311. Epub 2015 Oct 28.
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Perineal groove: A rare congenital abnormality of failure of fusion of the perineal raphe and discussion of its embryological origin.会阴沟:一种罕见的先天性异常,即会阴缝融合失败及其胚胎学起源的讨论。
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