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一名新生儿的梗阻性半阴道和同侧肾发育不全综合征

Obstructed Hemivagina and Ipsilateral Renal Agenesis Syndrome in a Neonate.

作者信息

Khanal Luna, Deora Kanika, Gaihre Suman R, Monika Bajaj

机构信息

Pediatrics, Children's Hospital of Michigan, Detroit, USA.

Neonatology, Central Michigan University College of Medicine, Mount Pleasant, USA.

出版信息

Cureus. 2023 Mar 28;15(3):e36822. doi: 10.7759/cureus.36822. eCollection 2023 Mar.

Abstract

Obstructed hemivagina with an ipsilateral renal anomaly (OHVIRA) syndrome is a congenital malformation that presents as a uterine didelphys with an obstructed hemivagina and an associated ipsilateral renal aberration. The clinical symptoms usually manifest after menarche. Unlike the typical presentation in adolescence, this case report features a neonatal presentation of OHVIRA syndrome with an unusual renal association. A female twin delivered at 35 weeks of gestation was transferred to our institution after birth from an outside hospital due to respiratory distress and for evaluation of the left multicystic dysplastic kidney identified on prenatal ultrasound. Physical examination and lab results, including a complete blood count, and a basic metabolic panel, including blood urea and serum creatinine, were within the normal range for age. Abdominal and pelvic ultrasound showed multicystic dysplastic left pelvic kidney, congenital hepatic cyst measuring 6 mm, uterine didelphys with duplication of the vaginal canal, and obstructed left hemivagina corresponding to the OHVIRA syndrome. Further testing revealed a normal chromosomal microarray, small patent foramen ovale on the echocardiogram, no vertebral or rib anomalies on the spinal x-ray, normal hearing test, and mild optic cupping on the ophthalmological evaluation. The pediatric surgeon and urologist recommended an outpatient follow-up and elective surgery in the future. This is a unique case presenting in the neonatal period with an unusual association. Timely intervention can help prevent obstetric complications.

摘要

梗阻性半阴道合并同侧肾异常(OHVIRA)综合征是一种先天性畸形,表现为双子宫伴梗阻性半阴道及相关同侧肾畸形。临床症状通常在初潮后出现。与青春期的典型表现不同,本病例报告呈现了OHVIRA综合征的新生儿表现及不寻常的肾脏关联。一名孕35周出生的女双胞胎因呼吸窘迫在出生后从外院转入我院,并对产前超声发现的左多囊性发育不良肾进行评估。体格检查和实验室检查结果,包括全血细胞计数以及包括血尿素和血清肌酐在内的基础代谢指标,均在该年龄的正常范围内。腹部和盆腔超声显示左盆腔多囊性发育不良肾、6mm先天性肝囊肿、双子宫伴阴道管重复以及与OHVIRA综合征相符的梗阻性左半阴道。进一步检查显示染色体微阵列正常、超声心动图显示小的卵圆孔未闭、脊柱X线检查未见椎体或肋骨异常、听力测试正常以及眼科评估有轻度视盘凹陷。小儿外科医生和泌尿外科医生建议门诊随访并择期手术。这是一例在新生儿期出现且有不寻常关联的独特病例。及时干预有助于预防产科并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c069/10139762/6c04edb15422/cureus-0015-00000036822-i01.jpg

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