双脊膜膨出-一种罕见的神经管缺损:一个病例系列

Q4 Medicine Journal of Neonatal Surgery Pub Date : 2022-11-29 DOI:10.47338/jns.v11.1126
Md Mokarram Ali, Y. Kadian
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引用次数: 0

摘要

背景:神经管缺损是一种常见的先天性畸形,通常表现为背部从枕骨到骶骨的孤立性囊性肿胀。然而,多发性神经管缺陷是罕见的,全世界报告的病例不到100例。病例介绍:我们报告了两例多发性神经管缺陷,发生在新生儿时期,有背部中线同时肿胀的病史。经超声检查,确诊为双脊膜膨出。随后,他们进行了手术,切除了两个病变,并同时修复了缺陷。结论:双脊膜膨出是一种罕见的神经管缺损。由于其稀有性,确切的胚胎发生尚不清楚,因此有必要对其胚胎学进行进一步研究。
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Double meningomyelocele - a rare variant of neural tube defect: A case series
Background: A neural tube defect is a common congenital malformation and it commonly presents as an isolated cystic swelling on the back, anywhere from occiput to sacrum. However, multiple neural tube defects are rare with less than 100 cases reported worldwide. Case Presentation: We are reporting two cases of multiple neural tube defects that presented in the newborn period with a history of concurrent swellings along the midline on the back. They were evaluated with ultrasonography and the diagnosis of double meningomyelocele was confirmed. Subsequently, they were operated on, both the lesions were excised, and the defects were repaired simultaneously. Conclusion: Double meningomyelocele is a rare form of neural tube defect. Due to its rarity, exact embryogenesis is not known and thus, there is a need for further study on its embryology.
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来源期刊
Journal of Neonatal Surgery
Journal of Neonatal Surgery Medicine-Surgery
CiteScore
0.30
自引率
0.00%
发文量
29
审稿时长
6 weeks
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