Case Report on Myleomeningiocele with Cerebellar Tonsillar

Ekta Ranagri, J. Gawai
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Abstract

Myelomeningocele is a form of neural tube abnormality that causes the spinal cord and meninges to protrude through a hole in the spinal column. It is uncommon for myelomeningocele to be associated with cerebellar tonsillar herniation. This instance demonstrates the difficulties in detecting and controlling this comorbid illness. Myelomeningocele with cerebellar tonsillar herniation is a severe congenital disorder involving the protrusion of the spinal cord and meninges through a defect in the vertebral column, accompanied by downward displacement of the cerebellar tonsils. It is associated with significant neurological and physical impairments, requiring comprehensive medical management and rehabilitation. Early diagnosis, intervention, and on-going multidisciplinary care are crucial for individuals affected by this condition to maximize their potential and improve their overall well-being. We present a case of a female child who was admitted to the NICU for further evaluation and management of myelomeningocele. On examination, the child was active with vitals stable. On local examination, swelling is present at the Lumbosacral region of size 5*4 cm. All investigations and septic screens sent reports within normal limits. MRI was done s/o Spina bifid occulta with LS myelomeningocele with cerebellar tonsillar descent (likely Arnold Chiari Malformation type.
小脑扁桃体伴脊膜脑膜膨出1例报告
脊髓脊膜膨出是神经管异常的一种形式,它会导致脊髓和脑膜从脊柱的孔中突出。脊髓脊膜膨出合并小脑扁桃体疝并不常见。这个例子说明了发现和控制这种共病的困难。脊髓脊膜膨出伴小脑扁桃体疝是一种严重的先天性疾病,涉及脊髓和脑膜通过脊柱缺陷突出,并伴有小脑扁桃体向下移位。它与严重的神经和身体损伤有关,需要全面的医疗管理和康复。早期诊断、干预和持续的多学科护理对受这种疾病影响的个体至关重要,以最大限度地发挥其潜力并改善其整体健康状况。我们提出一个病例的女性儿童谁被录取到新生儿重症监护室进一步评估和管理脊膜膨出。经检查,孩子活动自如,生命体征稳定。局部检查,腰骶区肿胀,大小为5* 4cm。所有的调查和化粪池检查报告都在正常范围内。MRI检查为隐匿性脊柱裂伴LS脊髓脊膜膨出伴小脑扁桃体下降(可能为Arnold Chiari畸形型)。
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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