1例男孩硬脊膜动静脉瘘及盲肠动静脉畸形

APSP journal of case reports Pub Date : 2017-01-04 DOI:10.21699/ajcr.v8i1.510

Vimlesh Soni, P. Vaidya, J. Sahu, M. Yadav, P. Singhi

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引用次数: 1

摘要

并发硬脊膜动静脉瘘(AVF)和盲肠动静脉畸形(AVM)是非常罕见的。一个六岁男孩在创伤后表现为下肢麻痹。影像学检查发现脊膜AVF。采用血管内胶栓塞治疗。两年后，男孩出现严重贫血和隐蔽性胃肠道出血。盲肠AVM的诊断和治疗与栓塞。

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Spinal Dural Arteriovenous Fistula and Cecal Arteriovenous Malformation in a Boy

Concurrent spinal dural arteriovenous fistula (AVF) and cecal arteriovenous malformation (AVM) are very rare. A 6-year old boy presented with lower limb paresis after trauma. On imaging work-up spinal dural AVF was found. It was managed with endovascular glue embolization. After two years, the boy presented with severe anemia and occult gastrointestinal tract (GIT) bleed. Cecal AVM was diagnosed and managed with embolization.

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APSP journal of case reports

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