左主干起源于右冠状动脉窦（附2例报告并文献复习）

目的:分析左主干起源于右冠状动脉窦的临床特征,提高对左主干起源于右冠状动脉窦的认识和诊断.方法:回顾分析2例左主干起源于右冠状动脉窦的临床病例并对文献进行回顾分析.结果:左主干起源于右冠状动脉窦是一种罕见的先天性冠脉畸形,这种畸形可分为良性或恶性,主要根据异常左冠状动脉与主动脉和肺动脉之间的关系.对于可能引起猝死或严重心肌缺血患者,应进行冠状动脉旁路移植术.2例患者左主干起源于右冠状动脉窦,其中1例左主干走行于主动脉与肺动脉之间,1例走行于主动脉前方,这2例未进行预防性外科手术,目前预后良好.结论:左主干起源于右冠状动脉窦是罕见的冠脉畸形,应注意鉴别是良性或是恶性,确定下一步治疗方案.     

Histopathology of the teeth in segmental odontomaxillary dysplasia: new findings

Histological examination of the deciduous teeth in two cases of segmental odontomaxillary dysplasia (SOMD) showed fibrous enlargement of the pulps, an irregular pulp/dentine interface displaying many pseudoinclusions and pulp stones. There were tubular defects in the coronal dentine from pulp horn to cusp tip, an irregular tubular structure to the circumpulpal dentine of the apical half, a focally deficient odontoblast layer and widespread external resorption. Together with the clinical features of unilateral maxillary enlargement, upper alveolar expansion in the distal segment, increased spacing and delayed eruption of the deciduous molars and absence of premolar teeth, these histological appearances allow distinction of this condition from fibrous dysplasia (FD), segmental hemifacial hypertrophy (SHH) and regional odontodysplasia (ROD).     

The assimilated os sustentaculi

The assimilated os sustentaculi is a projection of bone from the medial aspect of the sustentaculum tali which is surmounted by a similar projection from the medial tubercle of the talus. The accessory joint so formed may develop secondary osteoarthritis changes. This congenital anomaly is very rate. The present report is of 2 additional cases.     

Ebstein畸形82例心血管造影分析

报道我院1958～1992年期间的 Ebstein 畸形82例。平片表现可归纳为球型、方型和不典型4种心脏形态。介绍该畸形的心血管造影方法,所见征象和相应的病理基础。主要造影征象有:1.心脏膈面双切迹征;2.帆样征:3.房化心室:4.三尖瓣闭锁不全。本文结合文献对本病病理,X 线表现进行了系统的讨论,并着重突出了我们的观点。     

椎动脉形态学异常对后循环短暂性脑缺血发作症状持续时间的影响

目的 探讨椎动脉形态学异常对后循环TIA症状持续时间的影响。
方法 回顾性分析2015年10月-2018年3月在中国科学院大学重庆仁济医院神经内科完成头颈部DSA
或CTA的后循环TIA住院患者临床资料，根据症状持续时间分为<10 min组、10～59 min组和≥60 mi n组，
比较椎动脉形态异常各亚型在3组间的差异。通过多因素Logistic回归分析明确椎动脉形态异常与后
循环TIA症状持续时间之间的关系。
结果 共纳入237例患者，其中症状持续时间<10 min组109例（45.99%）、10～59 min组71例（29.96%）
和≥60 min组57例（24.05%）。一般临床资料的比较显示，性别、椎动脉和基底动脉狭窄率≥50%
在3组间差异具有统计学意义（P＜0.05）。椎动脉形态异常中，动脉粥样硬化性椎动脉狭窄（狭窄
率1%～99%）在3组间的差异具有统计学意义（P =0.004），而一侧迂曲、双侧迂曲、一侧优势、一
侧优势合并迂曲和起源异常在3组间差异均无统计学意义；多因素Logi sti c回归分析显示椎动脉
狭窄（OR 2.500，95%CI 1.381～4.525，P =0.002）、基底动脉狭窄率≥50%（OR 12.066，95%CI
1.446～100.668，P =0.021）是TI A症状持续时间延长的独立影响因素。
结论 椎动脉狭窄和基底动脉狭窄率≥50%是影响后循环TIA症状持续时间延长的独立影响因素。     

Klippel-Feil anomaly combined with fetal alcohol syndrome

Summary Alcohol is the most frequent and most important teratogenic noxa for the embryo and fetus. It may lead to deformation of all cells and organs. A case of Klippel-Feil anomaly associated with fetal alcohol syndrome is described. The diagnosis of Klippel-Feil anomaly, even a late diagnosis made on the basis of rare deformities, is very important as the affected patients are at a high risk of alcoholism. The combination of Klippel-Feil anomaly with numerous other syndromes and deformities suggests a basic general disorder of skeletal maturation. Diverse cases of Klippel-Feil anomaly possibly originate., in reality, in an unrecognzied fetal alcohol syndrome.     

小儿鞘状突畸形的一日住院手术

报告自1988年1月至1990年1月以一日往院手术治疗小儿鞘状突畸形159例,其中腹股沟疝120例,鞘膜水囊肿39例。小儿疝囊或未闭鞘状突高位结扎虽然是小儿外科最常见的基本手术,但有时也会遇到困难,发生较严重的并发症,不宜完全按门诊手术处理。一日住院手术治疗鞘状突畸形可以提高病床周转率,减少术后院内交叉感染。本文讨论了一日住院手术的适应症,实施方法及其对手术者和麻醉医师的要求。