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新生儿期的完全性内脏反位

Situs Inversus Totalis in the Neonatal Setting.

作者信息

Devera Jordan, Licandro Francesca, Ramos Jean, Taymoorian Hovik T, Yap Laurel G

机构信息

Obstetrics and Gynecology, Pediatrics, and Medicine, University of Medicine and Health Sciences, Camps, Basseterre, KNA.

Obstetrics and Gynecology, MedStar Harbor Hospital, Baltimore, USA.

出版信息

Cureus. 2021 Feb 23;13(2):e13516. doi: 10.7759/cureus.13516.

Abstract

Situs inversus totalis (SIT) is a rare condition of complete inversion and mirroring of normal human anatomy. The incidence is approximately 1 in 8,000 to 1 in 25,000 live births. SIT is inherited in an autosomal recessive pattern and is associated with multiple gene mutations. It is also commonly seen in a condition known as primary ciliary dyskinesia. A 39-year-old pregnant woman presented to the Labor and Delivery unit to rule out pre-eclampsia due to high blood pressure recordings in the office setting. The infant was delivered preterm at 36 weeks gestation via spontaneous vaginal delivery. The infant presented with symptoms of respiratory distress. The newborn was transferred to the neonatal intensive care unit (NICU) for further work-up and to rule in/rule out an etiology known as Wet Lung. Upon retrieving a chest X-ray for the newborn, the results demonstrated situs inversus totalis. The newborn was transferred to a level III NICU for further management and work-up for other potential etiologies. Situs inversus totalis was not seen on prenatal work-up. In summary, situs inversus totalis is a rare condition which can be associated with other detrimental conditions. In the future, if situs inversus totalis is detected in utero, patients should be instructed to deliver in a setting in which any possible etiology can be accommodated. Pediatricians should follow these infants closely and with caution as common presentations may be obscured due to complete inversion of normal human anatomy. It is also important to screen these infants for other etiologies which may present in later developmental stages such as bronchiectasis and respiratory infections.

摘要

全内脏反位(SIT)是一种罕见的正常人体解剖结构完全反转和镜像的情况。发病率约为每8000至25000例活产中有1例。SIT以常染色体隐性模式遗传,与多种基因突变相关。它也常见于一种称为原发性纤毛运动障碍的病症中。一名39岁的孕妇因在门诊测量血压高而前往分娩室排除先兆子痫。婴儿在妊娠36周时通过自然阴道分娩早产。婴儿出现呼吸窘迫症状。新生儿被转至新生儿重症监护病房(NICU)进行进一步检查,以确定/排除一种称为湿肺的病因。为新生儿进行胸部X光检查后,结果显示为全内脏反位。新生儿被转至三级NICU进行进一步管理和对其他潜在病因的检查。产前检查未发现全内脏反位。总之,全内脏反位是一种罕见病症,可能与其他有害病症相关。未来,如果在子宫内检测到全内脏反位,应指导患者在能够应对任何可能病因的环境中分娩。儿科医生应密切且谨慎地随访这些婴儿,因为正常人体解剖结构的完全反转可能会掩盖常见症状。对这些婴儿进行筛查以排除其他可能在后期发育阶段出现的病因,如支气管扩张和呼吸道感染,也很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/721c/7904504/c8803732a635/cureus-0013-00000013516-i01.jpg

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