Clinical Spectrum and Surgical Outcomes of Parasitic Twins in Early Infancy: Case Series and Experience from a Tertiary Care Center.

Q3 Medicine
Ashish Chhabra, Saalim Nazki, Shipra Galhotra, Lubna Samad, Saswati Behera
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引用次数: 0

Abstract

Background: Parasitic or heteropagus conjoined twins are an exceptionally rare congenital anomaly, with an estimated incidence of 1 in 1-2 million live births. These anomalies pose complex clinical and surgical challenges due to their varied anatomical presentations. Multidisciplinary evaluation and timely intervention are essential for favorable outcomes. The study aimed at clinical presentation, anatomical description, management, and outcomes of various heteropagus twins that were managed in a single tertiary care center.

Methods: This retrospective study included six patients diagnosed with heteropagus twinning. Antenatal ultrasonography (USG) findings were reviewed where available. Postnatal investigations included USG, magnetic resonance imaging, and two-dimensional echocardiography for anatomical delineation and cardiac evaluation. Surgical intervention was performed based on the anatomical site and complexity of attachment. Resected specimens were sent for histopathological examination.

Results: All patients presented in early infancy. Presentations were diverse: one had a sacral mass mimicking a myelomeningocele (rachipagus) containing intestinal loops; another had a limb, phallus, and testis with lipomeningocele; the third baby had an extra lower limb attached to the pelvis; the fourth baby had an accessory digit on the back; the fifth baby had rudimentary parasitic tissue near the perineum, and the last baby had a mandibular outgrowth resembling a distorted ill-formed face. All cases underwent successful surgical separation with good postoperative recovery. One of the babies succumbed to neonatal sepsis. All the patients are under a strict surveillance protocol with a minimum follow-up period of 3 years and longest being 8 years.

Conclusion: Heteropagus twins exhibit a wide range of anatomical variations. Early antenatal diagnosis, detailed imaging, and prompt surgical management are key to achieving favorable outcomes. In addition, preoperative planning must include a detailed anatomical survey through the radiological scans and also cardiac evaluation. Surgical procedure to separate the parasitic twin varies from a simple to a more complex approach, so a multidisciplinary approach ensures comprehensive care and minimizes morbidity.

婴儿早期寄生双胞胎的临床谱和手术结果:来自三级保健中心的病例系列和经验。
背景:寄生或异位连体双胞胎是一种非常罕见的先天性异常,估计发病率为1- 200万活产婴儿。这些异常由于其不同的解剖表现,给临床和手术带来了复杂的挑战。多学科评估和及时干预是获得良好结果的必要条件。本研究的目的是临床表现,解剖描述,管理和结果在一个单一的三级护理中心管理的各种异胎双胞胎。方法:对6例诊断为异位双胞胎的患者进行回顾性研究。产前超声检查(USG)的结果进行审查,如有可能。产后检查包括超声心动图、磁共振成像和二维超声心动图,用于解剖描绘和心脏评估。根据附着的解剖位置和复杂程度进行手术干预。切除标本送组织病理检查。结果:所有患者均出现在婴儿期早期。表现多种多样:一个有类似髓膜膨出的骶骨肿块,包含肠袢;另一个有肢体、阴茎和睾丸,并伴有脂肪脊膜膨出;第三个婴儿的下肢与骨盆相连;第四个婴儿的背上有副手指;第五个婴儿在会阴附近有初步的寄生组织,最后一个婴儿的下颌骨长出了一个变形的畸形脸。所有病例均手术分离成功,术后恢复良好。其中一个婴儿死于新生儿败血症。所有患者均在严格的监测方案下,随访时间最短3年,最长8年。结论:异龙双胞胎具有广泛的解剖变异。早期产前诊断,详细的影像和及时的手术处理是取得良好结果的关键。此外,术前计划必须包括通过放射扫描和心脏评估进行详细的解剖调查。分离寄生双胞胎的手术程序从简单到更复杂的方法各不相同,因此多学科方法可确保全面护理并将发病率降至最低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Indian Association of Pediatric Surgeons
Journal of Indian Association of Pediatric Surgeons Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.80
自引率
0.00%
发文量
148
审稿时长
30 weeks
期刊介绍: Journal of Indian Association of Pediatric Surgeons is the official organ of Indian Association of Pediatric Surgeons. The journal started its journey in October 1995 under the Editor-in-Chief Prof. Subir K Chatterjee. An advisory board was formed with well-versed internationally reputed senior members of our society like Late Prof. R K Gandhi, Prof. I C Pathak, Prof. P Upadhyay, Prof. T Dorairajan and many more. since then the journal is published quarterly uninterrupted. The journal publishes original articles, case reports, review articles and technical innovations. Special issues on different subjects are published every year. There have been several contributions from overseas experts.
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