Saurya Saurya, Dhamija Bhumika, Sharma Srishti, Singh Ravi S, Ks Priyanka, Kumar Saroj, Siddhant Kumar, Haque Sumair
Department of Radiodiagnosis, All India Institute of Medical Sciences, Patna, Patna, IND.
Department of Radiodiagnosis, All India Institute of Medical Sciences, Rishikesh, Rishikesh, IND.
Cureus. 2024 Oct 6;16(10):e70924. doi: 10.7759/cureus.70924. eCollection 2024 Oct.
Objective This study aims to evaluate the MRI morphology of corpus callosum malformations and the associated anomalies frequently observed in a tertiary care center in northern India. Methods We conducted a retrospective cross-sectional study using MRI reports, images, and clinical records from January 2020 to July 2024. A total of 19 patients with corpus callosum agenesis or hypoplasia were identified, with 17 patients included after excluding those with incomplete records. We analyzed MRI findings for agenesis type (complete or partial), commissural abnormalities, midline anomalies, cortical abnormalities, and posterior fossa abnormalities. Statistical analysis was performed using chi-square tests to compare associations between complete and partial agenesis. Results Of the 17 patients, 52.9% had complete agenesis and 47.1% had partial agenesis. Complete agenesis was associated with higher rates of commissural involvement (44.4% vs. 12.5%), midline anomalies (22.2% vs. 0%), and Probst bundle formation (88.9% vs. 37.5%). Ventricular distortion was more common in complete agenesis (88.9% vs. 40%), and cortical malformations were also more prevalent (44.4% vs. 12.5%). Other anomalies included holoprosencephaly, Dandy-Walker malformation, and hypoxic-ischemic encephalopathy changes. Conclusion Complete agenesis of the corpus callosum is significantly associated with other commissural abnormalities, midline cysts, Probst bundle formation, ventricular distortions, and cortical malformations compared to partial agenesis. This study highlights the varied imaging presentations of corpus callosum malformations and their associated anomalies.
目的 本研究旨在评估胼胝体发育不全的MRI形态以及在印度北部一家三级医疗中心经常观察到的相关异常情况。方法 我们使用2020年1月至2024年7月的MRI报告、图像和临床记录进行了一项回顾性横断面研究。共确定了19例胼胝体发育不全或发育不良的患者,排除记录不完整的患者后,纳入了17例患者。我们分析了发育不全类型(完全或部分)、连合异常、中线异常、皮质异常和后颅窝异常的MRI表现。使用卡方检验进行统计分析,以比较完全发育不全和部分发育不全之间的关联。结果 17例患者中,52.9%为完全发育不全,47.1%为部分发育不全。完全发育不全与更高的连合受累率(44.4%对12.5%)、中线异常(22.2%对0%)和普罗布斯特束形成率(88.9%对37.5%)相关。脑室变形在完全发育不全中更常见(88.9%对40%),皮质畸形也更普遍(44.4%对12.5%)。其他异常包括前脑无裂畸形、丹迪-沃克畸形和缺氧缺血性脑病改变。结论 与部分发育不全相比,胼胝体完全发育不全与其他连合异常、中线囊肿、普罗布斯特束形成、脑室变形和皮质畸形显著相关。本研究强调了胼胝体发育不全及其相关异常的多种影像学表现。