Parasitic Craniopagus with Cervical Myelomeningocele and Hydrocephalus: Reporting the rarely Reported

Aliyu Muhammad Koko, Ali Lasseini, Nasiru Jinjiri Isma, Bello Bala Shehu
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 Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus.
 Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome.
 Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele
 Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus.
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Abstract

Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus. Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome. Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus. Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome.
寄生虫性颅裂伴颈髓脊膜膨出及脑积水:罕见报道
目的:寄生虫性颅斜视是一种极其罕见的神经外科疾病,其他异常如脑积水和脊膜膨出使其更加罕见和复杂的管理。本报告的目的是描述一个儿童成功的管理与颅寄生,先天性脑积水和颈髓脊膜脑炎三联征;病例介绍:我们成功地治疗了一例5个月大的女婴,该女婴患有寄生虫性颅瘘、颈髓脊膜膨出和先天性脑积水。结论:寄生性颅锥仍是一种少见的神经外科疾病,可合并许多先天性异常,如脑积水和脊膜膨出,仔细的评估和处理将带来良好的结果。目的:寄生虫性颅斜视是一种极其罕见的神经外科疾病,其他异常如脑积水和脊膜膨出使其更加罕见和复杂的管理。本报告的目的是描述一个儿童成功的管理与颅寄生,先天性脑积水和颈髓脊膜脑炎三联征;病例介绍:我们成功地治疗了一例5个月大的女婴,该女婴患有寄生虫性颅瘘、颈髓脊膜膨出和先天性脑积水。结论:寄生性颅裂是一种少见的神经外科疾病,可合并许多先天性异常,如脑积水和脊膜膨出,仔细的评估和处理将会带来良好的结果。
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