Journals / Cukurova Medical Journal / 2015 / Cilt: 40 - Sayı: 2

Split Cord Malformations

Ayrık Omurilik Malformasyonu

Pages
199–207
Publication Date
2015-09-10
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Earlier diagnosis, meticuolus surgical therapy and interdisciplinary careful evaluation and follow-up should be made for good prognosis

📌 3 Key Takeaways

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Objective & Hypothesis:Split cord malformations are rare form of occult spinal dysraphism in children.
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Key Findings & Data:Although their precise incidence is unknown, split cord malformations are exceedingly rare and represent %3.8-5 of all congenital spinal anomalies.
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Conclusion & Impact:Earlier diagnosis, meticuolus surgical therapy and interdisciplinary careful evaluation and follow-up should be made for good prognosis
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Split cord malformation · spinal dysraphism · spina bifida

Abstract

Split cord malformations are rare form of occult spinal dysraphism in children. Split cord malformations are characterized by septum that cleaves the spinal canal in sagittal plane within the single or duplicated thecal sac. Although their precise incidence is unknown, split cord malformations are exceedingly rare and represent %3.8-5 of all congenital spinal anomalies. Characteristic neurological, urological, orthopedic clinical manifestations are variable and asymptomatic course is possible. Earlier diagnosis and surgical intervention for split cord malformations is associated with better long-term fuctional outcome. For this reason, diagnostic imaging is indicated for children with associated cutaneous and orthopedic signs. Additional congenital anomalies usually to accompany the split cord malformations. Earlier diagnosis, meticuolus surgical therapy and interdisciplinary careful evaluation and follow-up should be made for good prognosis

Özet

Ayrık omurilik malformasyonu (AOM); çocukluk çağında görülen okkült spinal disrafizmin nadir bir formudur. AOM tek veya çift dural kılıf içerisinde, omuriliğin iki ayrı yarıdan oluştuğu konjenital anomaliyi tanımlar. Kesin insidansı bilinmemekle birlikte nadirdir, tüm gelişimsel spinal anomalilerin %3.8-5’ ni oluşturur. Asemptomatik kalabileceği gibi karakteristik nörolojik, ürolojik ve ortopedik yakınmalara neden olabilir. Bu problemlerin gelişmesinin önüne geçilebilmesi malformasyonun erken teşhis ve tedavisine bağlıdır. Erken teşhis için yeni doğan dönemindeki bebeklerin cilt ve ortopedik bulgularına dikkat edilmeli ve gerekirse tüm nöral aks radyolojik olarak incelenmelidir. AOM’ na sıklıkla gergin omurilik sendromuna neden olan ilave patolojiler de eşlik eder. Erken teşhis, titiz cerrahi yaklaşım ve hastanın beyin cerrahi, ortopedi, çocuk nefroloji, üroloji hekimlerinden oluşan bir ekip tarafından yakın takip ve tedavisi ile başarılı sonuçlar elde edilir

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Cite This Article

GEZERCAN, Y., ÖZSOY, K., OKTAY, K., ÇETİNALP, N., ERMAN, T., ZEREN, M. (2015). Split Cord Malformations. Cukurova Medical Journal, Cilt: 40 - Sayı: 2, 199–207. https://ajindex.com/articles/216041

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References (5)

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