高密度多孔聚乙烯植入体在鼻整形中的应用

目的 探究高密度多孔聚乙烯植入体在鼻整形中的应用价值方法 选取2019年5月-2021年8月我院接受综合鼻整形手术的106例患者为研究对象，采用照随机数字表法分为对照组和观察组，各53例。 对照组采用自体肋骨植入术，观察组采用高密度多孔聚乙烯植入体植入治疗，比较两组临床手术指标(手术时间、恢复时间)、整形优良率、鼻指标(鼻高度/鼻长度比例、鼻唇角)、并发症发生率以及疼痛评分结果 观察组手术时间、术后恢复时间均短于对照组(P＜0.05)；观察组整形优良率为94.34%，高于对照组的86.79%，差异有统计学意义(P＜0.05)；观察组鼻高度/鼻长度比例高于对照组，鼻唇角小于对照组，差异有统计学意义(P＜0.05)；观察组并发症发生率为5.66%，低于对照组的15.09%，差异有统计学意义(P＜0.05)；观察组疼痛评分低于对照组，差异有统计学意义(P＜0.05)；观察组治疗满意度为 96.23%，高于对照组的84.91%，差异有统计学意义(P＜0.05)结论 高密度多孔聚乙烯植入体在鼻整形中的应用效果理想，可减轻患者疼痛度，缩短手术和恢复时间，降低并发症发生率，改善鼻高度/鼻长度比例和鼻唇角，实现理想的整形效果。     

胫腓骨下段开放性粉碎骨折的治疗(附20例临床报告)

目的探讨胫腓骨下段开放性粉碎骨折的综合治疗。方法20例胫腓骨下段开放性粉碎骨折采用半环槽式外固定器固定、皮瓣转移、腓骨内移、骨折端加压并同期行上干骺端骨延长等综合治疗方法。结果伤口均一期愈合，所有皮瓣均成活，骨折临床愈合平均时间19周，7例因严重骨缺损经骨折端加压并同期行上干骺端骨延长后肢体均恢复正常长度。无1例针眼感染和血管、神经损伤。临床优良率为90％(18／20)。结论a)半环槽外固定器能克服胫腓骨下段开放性粉碎骨折的治疗困难，具有立体均衡固定。刚性可调，避免肢体受压。便于再次创面处理以及同期行骨折端加压和肢体延长等优点。b)半环槽式外固定器结合皮瓣转移、腓骨内移以及骨折端加压并同期行上干骺端骨延长等综合治疗方法是胫腓骨下段开放性粉碎骨折可选择的较好治疗措施之一。     

重视膀胱癌淋巴管浸润和淋巴结转移的研究

转移是膀胱癌患者死亡的主要原因,且早期以淋巴结转移为主。T2 期膀胱癌约 50%淋巴管内有癌细胞,T3 期几乎全部淋巴管内有癌细胞。残存的肿瘤细胞淋巴管浸润是肿瘤切除术后复发的根源,明显的淋巴结转移更是患者预后不良的重要危险因素。然而膀胱癌淋巴管浸润和淋巴结转移的     

碘伏用于超声根管预备预防根管治疗期间痛的临床研究

目的观察碘伏用于超声根管预备对死髓牙根管治疗期间痛(endodontic interappointment pain EIP)发生率的影响及防治效果.方法对159例180颗慢性根尖周炎患者,随机分为3组(每组60颗患牙).第1组为传统手持器械对照组,第2组为超声生理盐水对照组,第3组为超声碘伏治疗组.采用临床观察分析法,观察治疗组与对照组临床反应的差异.结果超声治疗组Ⅱ～Ⅲ级EIP发生率为10%,对照组为36.67%(P＜0.01),有显著差异性.结论碘伏应用于超声根管预备能预防和降低EIP的发生并减轻其疼痛程度.     

Spondylometaphyseal dysplasia: further heterogeneity

The spondylometaphyseal dysplasias are a very heterogeneous group of disorders. Only one has been clearly defined, namely, the spondylometaphyseal dysplasia — Kozlowski type, known also as the common type. This disorder is inherited as an autosomal dominant trait. In this report we describe an Arabic-Moslem kindred with spondylometaphyseal dysplasia, not of the common type, with an autosomal dominant mode of inheritance, indicating further heterogeneity.     

New multiple congenital anomalies: Mental retardation syndrome (MCA/MR) with facio-cutaneous-skeletal involvement

Five unrelated patients (a male and 4 females) were affected with a previously undefined multiple congenital anomalies/mental retardation syndrome which has been designated the facio-cutaneous-skeletal (FCS) syndrome and which includes mental retardation with specific sociable, humorous behavior, characteristic facial appearance, excessive generalized skin, postnatal growth failure, and skeletal involvement. Consanguinity was noted in 2 patients, thus autosomal recessive inheritance is suggested. © 1992 Wiley-Liss, Inc.     

Springer Link及其收录的医学期刊分析

目的：向图书馆员和用户介绍Springer Link，对其收录的医学期刊进行深入分析，使该数据库得到更好的利用。方法利用《外国报刊目录》和美国《医学索引》(IM)的《引用期刊一览表》等对Springer Link收录的英文医学期刊从权威性、出版地分布、学科分布和收藏年限等方面进行考查。结果86％的期刊被IM引用，欧洲——尤其是德国的期刊较多，医学各学科都有相应的期刊被收录，但数量分布不均，有所偏重，72．7％的期刊可以保证至少近5年或自创刊以来的文献。结论Springer Link所提供的全文医学期刊服务质量较上乘，并有自己的特色。     

Neu-Laxova syndrome: Prenatal ultrasonographic diagnosis,clinical and pathological studies,and new manifestations

A diagnosis of the Neu-Laxova syndrome (NLS) was made by ultrasonography at 32 wks of gestation. Ultrasonographic examination showed intrauterine growth retardation (IUGR), Dandy-Walker anomaly, choroid plexus cysts, receding forehead and microcephaly, bilateral cataract without prominent eyes, scalp edema with no generalized edema, retrognathia, curved penis, and flexion deformities of limbs. The findings in this case are consistent with NLS; however, they did not fit any of Curry's [1982] groups. Massive swelling of hands and feet were among the main manifestations in classic NLS cases. In the case presented herein, edema was noted only in the scalp. This might shed further light on the question of variability vs. heterogeneity in the NLS. This case shows the existing possibility of an early diagnosis of NLS and adds Dandy-Walker anomaly and choroid plexus cysts as new findings to this syndrome. © 1992 Wiley-Liss, Inc.