先天性内管:一种异常,目前还很难被识别
Alessandro Raffaele1, Marta Gazzaneo1, Piero Romano1
1Pediatric Surgery Unit, Department of Maternal and Child Health, Fondazione IRCCS Policlinico San Matteo, Pavia, Lombardia, Italy.
先天性内喉瘤 (CIJP) 是一种罕见的部质. 建议对无症状病例进行保守管理,并定期进行临床和超声监测.
科学领域:
- 血管外科 血管外科
- 儿科放射学 儿科放射学
- 医学诊断 医学诊断 医学诊断
背景情况:
- 先天性内喉 (CIJP) 是一种罕见的静脉形.
- 它呈现为侧侧部质量,往往由应力加剧.
- 诊断可能会延迟几个月到几年,许多病例是无症状的.
研究的目的:
- 在儿科患者中报告CIJP病例.
- 为了突出诊断成像的发现.
- 讨论无症状CIJP的保守管理策略.
主要方法:
- 一个7岁男孩的病例介绍,他的部有侧面质量.
- 诊断成像包括部超声波 (US) 和对比度增强计算机断层扫描 (CT) 扫描.
- 保守管理,随访5年.
主要成果:
- 美国公布了右内关节轴心,随着瓦萨尔瓦机动而恶化.
- CT证实了右侧内静脉的状扩张.
- 在5年的随访期间,患者仍然无症状,没有并发症.
结论:
- CIJP是一种罕见的疾病,通常是偶然或延迟后诊断出来的.
- 无症状CIJP可以保守地管理,因为它的自我限制性质.
- 定期的临床和美国评估对于监测无症状CIJP患者至关重要.
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