首页 > 最新文献
paperpass

La Chirurgia degli organi di movimento最新文献

英文 中文
Distal osteotomy of the first metatarsal bone in association with sub-talar arthroerisis, for hallux valgus correction in abnormal pronation syndrome. 第一跖骨远端截骨与距下关节关节病相关,用于异常前旋综合征拇外翻矫正。
Pub Date : 2008-12-01 Epub Date: 2008-12-10 DOI: 10.1007/s12306-008-0065-0
Carlo Lucaccini, Nevio Zambianchi, Gabriele Zanotti

The Authors analyse the clinical and radiographical results of 14 patients (16 feet) affected by hallux valgus (HV) in flexible abnormal pronation syndrome. Patients were treated by distal osteotomy of the first metatarsal bone and sub-talar arthroerisis in one stage. This treatment was chosen because HV is often associated with abnormal foot pronation. Patients were young and the sub-talar joints had good mobility. The protocol forecasts: X-ray study of the feet and post-surgery planning, day surgery admission, minimally invasive surgery and 5 weeks of immobilisation in a below-knee cast.

作者分析了14例(16英尺)拇外翻(HV)患者柔性异常旋前综合征的临床和影像学结果。患者采用第一跖骨远端截骨术和距下关节关节病一期治疗。选择这种治疗是因为HV通常与异常足内旋有关。患者年龄小,距下关节活动度好。该方案预测:足部x线检查和术后计划,日间手术入院,微创手术和膝盖以下石膏固定5周。
{"title":"Distal osteotomy of the first metatarsal bone in association with sub-talar arthroerisis, for hallux valgus correction in abnormal pronation syndrome.","authors":"Carlo Lucaccini,&nbsp;Nevio Zambianchi,&nbsp;Gabriele Zanotti","doi":"10.1007/s12306-008-0065-0","DOIUrl":"https://doi.org/10.1007/s12306-008-0065-0","url":null,"abstract":"<p><p>The Authors analyse the clinical and radiographical results of 14 patients (16 feet) affected by hallux valgus (HV) in flexible abnormal pronation syndrome. Patients were treated by distal osteotomy of the first metatarsal bone and sub-talar arthroerisis in one stage. This treatment was chosen because HV is often associated with abnormal foot pronation. Patients were young and the sub-talar joints had good mobility. The protocol forecasts: X-ray study of the feet and post-surgery planning, day surgery admission, minimally invasive surgery and 5 weeks of immobilisation in a below-knee cast.</p>","PeriodicalId":76085,"journal":{"name":"La Chirurgia degli organi di movimento","volume":"92 3","pages":"145-8"},"PeriodicalIF":0.0,"publicationDate":"2008-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12306-008-0065-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27899992","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Medial meniscal cyst: a case report. 内侧半月板囊肿1例。
Pub Date : 2008-12-01 Epub Date: 2008-11-15 DOI: 10.1007/s12306-008-0059-7
Mauro Spina, Giacomo Sabbioni, Domenico Tigani

Meniscal cysts are a rare disease constantly combined with a horizontal meniscal lesion. Currently, nuclear magnetic resonance (MRI) is the main diagnostic tool, because of its high sensitivity and specificity, and decompression arthroscopy combined with selective meniscectomy is the treatment of choice. The Authors report a case of a voluminous medial meniscal cyst where instrumental examination, MRI, was fundamental for the preoperative diagnosis of the horizontal meniscal lesion causing the cystic degeneration of the meniscus. The treatment performed was selective meniscectomy of the body and posterior horn of the medial meniscus and decompression of the voluminous cyst by arthroscopy. Physical examination after six months showed the complete resolution of swelling at the medial hemirima, no walking pain and normal range of motion.

半月板囊肿是一种罕见的疾病,经常合并水平半月板病变。目前,核磁共振(MRI)是主要的诊断工具,因其具有较高的敏感性和特异性,减压关节镜联合选择性半月板切除术是治疗的首选。作者报告了一例巨大的内侧半月板囊肿,其中仪器检查,MRI,是术前诊断水平半月板病变导致半月板囊性变性的基础。治疗方法为选择性半月板体和内侧半月板后角切除术,关节镜下对大囊肿进行减压。6个月后的体格检查显示内侧半边肿胀完全消退,无行走疼痛,活动范围正常。
{"title":"Medial meniscal cyst: a case report.","authors":"Mauro Spina,&nbsp;Giacomo Sabbioni,&nbsp;Domenico Tigani","doi":"10.1007/s12306-008-0059-7","DOIUrl":"https://doi.org/10.1007/s12306-008-0059-7","url":null,"abstract":"<p><p>Meniscal cysts are a rare disease constantly combined with a horizontal meniscal lesion. Currently, nuclear magnetic resonance (MRI) is the main diagnostic tool, because of its high sensitivity and specificity, and decompression arthroscopy combined with selective meniscectomy is the treatment of choice. The Authors report a case of a voluminous medial meniscal cyst where instrumental examination, MRI, was fundamental for the preoperative diagnosis of the horizontal meniscal lesion causing the cystic degeneration of the meniscus. The treatment performed was selective meniscectomy of the body and posterior horn of the medial meniscus and decompression of the voluminous cyst by arthroscopy. Physical examination after six months showed the complete resolution of swelling at the medial hemirima, no walking pain and normal range of motion.</p>","PeriodicalId":76085,"journal":{"name":"La Chirurgia degli organi di movimento","volume":"92 3","pages":"175-8"},"PeriodicalIF":0.0,"publicationDate":"2008-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12306-008-0059-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27841664","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Synovial chondrosarcoma of the hip: report of two cases and literature review. 髋关节滑膜软骨肉瘤2例报告并文献复习。
Pub Date : 2008-12-01 Epub Date: 2008-12-04 DOI: 10.1007/s12306-008-0062-3
Domenico Andrea Campanacci, Davide Matera, Alessandro Franchi, Rodolfo Capanna

Synovial chondrosarcoma (SCH) is a rare malignant tumour. The lesion may arise de novo in intra-articular space or, more frequently, it may occur as a malignant degeneration of synovial chondromatosis (SC). The authors report two cases of SCH of the hip joint occurring on a SC diagnosed 23 years earlier in one case and 10 years earlier in another case. In both cases the SCH showed an intermediate grade of malignancy at histology (grade 2). In the first case, the patient underwent an external hemipelvectomy and he was disease-free 10 years after the operation. In the second case, the patient refused the proposed amputation and, after palliative radiation therapy, she was alive with disease 58 months after diagnosis. A review of literature reports on SCH was carried out. The knee was the most affected joint, followed by the hip. An amputation was performed in two thirds of cases. Amputation was done as primary surgery in one fifth of cases and for tumour recurrence after synovectomy in four fifth of cases. Metastatic dissemination was seen in 29% of cases. An early detection of malignant transformation of SC might improve the rate of limb salvage surgery in these patients, although no reliable clinical and imaging signs of malignant degeneration have been identified so far.

摘要滑膜软骨肉瘤是一种罕见的恶性肿瘤。病变可能发生在关节内间隙,或者更常见的是,它可能发生为滑膜软骨瘤病(SC)的恶性变性。作者报告了2例髋关节SCH,其中1例发生在23年前诊断的SC,另1例发生在10年前。在这两个病例中,SCH在组织学上显示为中度恶性肿瘤(2级)。在第一个病例中,患者接受了外半骨盆切除术,手术后10年无疾病。在第二个病例中,患者拒绝了建议的截肢,在姑息性放射治疗后,她在诊断后58个月仍然活着。本文对SCH的文献报道进行了综述。膝关节是受影响最严重的关节,其次是髋关节。三分之二的病例进行了截肢。五分之一的病例以截肢作为主要手术,五分之四的病例以滑膜切除术后肿瘤复发作为主要手术。29%的病例出现转移性传播。早期发现SC的恶性转化可能会提高这些患者的保肢手术率,尽管到目前为止还没有确定可靠的临床和影像学恶性变性迹象。
{"title":"Synovial chondrosarcoma of the hip: report of two cases and literature review.","authors":"Domenico Andrea Campanacci,&nbsp;Davide Matera,&nbsp;Alessandro Franchi,&nbsp;Rodolfo Capanna","doi":"10.1007/s12306-008-0062-3","DOIUrl":"https://doi.org/10.1007/s12306-008-0062-3","url":null,"abstract":"<p><p>Synovial chondrosarcoma (SCH) is a rare malignant tumour. The lesion may arise de novo in intra-articular space or, more frequently, it may occur as a malignant degeneration of synovial chondromatosis (SC). The authors report two cases of SCH of the hip joint occurring on a SC diagnosed 23 years earlier in one case and 10 years earlier in another case. In both cases the SCH showed an intermediate grade of malignancy at histology (grade 2). In the first case, the patient underwent an external hemipelvectomy and he was disease-free 10 years after the operation. In the second case, the patient refused the proposed amputation and, after palliative radiation therapy, she was alive with disease 58 months after diagnosis. A review of literature reports on SCH was carried out. The knee was the most affected joint, followed by the hip. An amputation was performed in two thirds of cases. Amputation was done as primary surgery in one fifth of cases and for tumour recurrence after synovectomy in four fifth of cases. Metastatic dissemination was seen in 29% of cases. An early detection of malignant transformation of SC might improve the rate of limb salvage surgery in these patients, although no reliable clinical and imaging signs of malignant degeneration have been identified so far.</p>","PeriodicalId":76085,"journal":{"name":"La Chirurgia degli organi di movimento","volume":"92 3","pages":"139-44"},"PeriodicalIF":0.0,"publicationDate":"2008-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12306-008-0062-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27879324","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 27
Adamantinoma: an unusual bone tumour. 金刚瘤:一种罕见的骨肿瘤。
Pub Date : 2008-12-01 Epub Date: 2008-11-15 DOI: 10.1007/s12306-008-0060-5
Pedro Roque, Henry J Mankin, Andrew Rosenberg

Adamantinoma is a rare tumour, which most often affects the tibia and produces lytic and sometimes destructive lesions, which can cause fractures. The lesions occur principally in adults and are more common in males. A small percentage of the patients develop metastases, sometimes quite late in the course. Our institution has treated 42 patients with adamantinomas since 1972 and has evaluated them by imaging studies and histology. The majority of the patients were treated by resection of the lesion and insertion of an intercalary allograft. Only three of the patients died of disease with the time until death ranging from 10 to 17 years. Recurrence occurred in only three patients and the allograft success rate in terms of function was 71% at a mean time of 10 years.

金刚烷瘤是一种罕见的肿瘤,它最常影响胫骨,并产生溶解性,有时是破坏性的病变,这可能导致骨折。这种病变主要发生在成人中,在男性中更为常见。一小部分患者发生转移,有时在病程很晚。自1972年以来,我们已经治疗了42例金刚烷瘤患者,并通过影像学研究和组织学对他们进行了评估。大多数患者通过切除病变并植入肾间异体移植物进行治疗。只有3例患者死于疾病,死亡时间从10年到17年不等。只有3例患者复发,在平均10年的时间里,同种异体移植的功能成功率为71%。
{"title":"Adamantinoma: an unusual bone tumour.","authors":"Pedro Roque,&nbsp;Henry J Mankin,&nbsp;Andrew Rosenberg","doi":"10.1007/s12306-008-0060-5","DOIUrl":"https://doi.org/10.1007/s12306-008-0060-5","url":null,"abstract":"<p><p>Adamantinoma is a rare tumour, which most often affects the tibia and produces lytic and sometimes destructive lesions, which can cause fractures. The lesions occur principally in adults and are more common in males. A small percentage of the patients develop metastases, sometimes quite late in the course. Our institution has treated 42 patients with adamantinomas since 1972 and has evaluated them by imaging studies and histology. The majority of the patients were treated by resection of the lesion and insertion of an intercalary allograft. Only three of the patients died of disease with the time until death ranging from 10 to 17 years. Recurrence occurred in only three patients and the allograft success rate in terms of function was 71% at a mean time of 10 years.</p>","PeriodicalId":76085,"journal":{"name":"La Chirurgia degli organi di movimento","volume":"92 3","pages":"149-54"},"PeriodicalIF":0.0,"publicationDate":"2008-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12306-008-0060-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27858211","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 9
Traumatic lumbosacral lateral dislocation without fracture. 外伤性腰骶外侧脱位无骨折。
Pub Date : 2008-12-01 Epub Date: 2008-11-27 DOI: 10.1007/s12306-008-0063-2
Federico De Iure, Stefania Paderni, Alessandro Gasbarrini, Stefano Bandiera, Stefano Boriani

Study design: A unique case of lumbosacral lateral dislocation without fracture is reported.

Objective: To report on the diagnosis and treatment of a traumatic L5-S1 lateral dislocation in a polytrauma 34-year-old male with L5 nerve root paralysis.

Method: Interbody fusion following decompression, posterior reduction and interbody grafting combined with posterior plating was performed.

Results: At an early stage the patient was able to return to work and walk without supports. At the 12-month follow-up evaluation no back pain was referred and fusion was achieved.

Conclusions: Lateral pure dislocation of the lumbosacral joint is very rare and can be easily misdiagnosed. A careful evaluation of the AP standard X-ray can lead to diagnosis and can be confirmed by CT scan. Prompt reduction and fusion is the treatment of choice to allow a quick functional recovery.

研究设计:报告一例独特的腰骶外侧脱位无骨折。目的:报道一例34岁男性多发创伤伴L5神经根麻痹的外伤性L5- s1侧位脱位的诊断和治疗。方法:行椎间融合术后减压、后路复位、椎间植骨联合后路钢板。结果:在早期阶段,患者能够返回工作和行走没有支持。在12个月的随访评估中,没有出现背部疼痛,并实现了融合。结论:单纯腰骶关节外侧脱位非常罕见,且易误诊。仔细评估AP标准x线片可导致诊断,并可通过CT扫描确认。快速复位融合是快速功能恢复的治疗选择。
{"title":"Traumatic lumbosacral lateral dislocation without fracture.","authors":"Federico De Iure, Stefania Paderni, Alessandro Gasbarrini, Stefano Bandiera, Stefano Boriani","doi":"10.1007/s12306-008-0063-2","DOIUrl":"10.1007/s12306-008-0063-2","url":null,"abstract":"<p><strong>Study design: </strong>A unique case of lumbosacral lateral dislocation without fracture is reported.</p><p><strong>Objective: </strong>To report on the diagnosis and treatment of a traumatic L5-S1 lateral dislocation in a polytrauma 34-year-old male with L5 nerve root paralysis.</p><p><strong>Method: </strong>Interbody fusion following decompression, posterior reduction and interbody grafting combined with posterior plating was performed.</p><p><strong>Results: </strong>At an early stage the patient was able to return to work and walk without supports. At the 12-month follow-up evaluation no back pain was referred and fusion was achieved.</p><p><strong>Conclusions: </strong>Lateral pure dislocation of the lumbosacral joint is very rare and can be easily misdiagnosed. A careful evaluation of the AP standard X-ray can lead to diagnosis and can be confirmed by CT scan. Prompt reduction and fusion is the treatment of choice to allow a quick functional recovery.</p>","PeriodicalId":76085,"journal":{"name":"La Chirurgia degli organi di movimento","volume":"92 3","pages":"183-5"},"PeriodicalIF":0.0,"publicationDate":"2008-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27864933","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Historical review of bone prefabrication. 骨预制的历史回顾。
Pub Date : 2008-09-01 Epub Date: 2008-08-30 DOI: 10.1007/s12306-008-0052-5
Claudia Di Bella, Enrico Lucarelli, Davide Donati

Prefabricated tissue represents a bridge between traditional reconstructive surgery and tissue engineering. Initially used in the 1960s in reconstructive plastic surgery, in the 1980s it was also used in orthopedics. The term "prefabricated" indicates a process of neovascularization of a tissue by implanting a vascular pedicle inside the tissue itself; this tissue can be then reimplanted either at a short distance through the pedicle itself, or as a free graft by microvascular anastomosis. The purpose of prefabrication is to build a tissue (muscle, bone, skin, or composite) with characteristics as similar as possible to those of the defect to fill, thus minimizing morbidity in the donor site and improving the reconstructive effectiveness. We present a review of the literature that includes the main experiments performed until now in which a bone segment has been reconstructed using scaffolds and growth factors in relationship to the local blood supply or to the use of a vascular pedicle.

预制组织是传统重建外科和组织工程之间的桥梁。最初在20世纪60年代用于重建整形手术,在20世纪80年代也用于矫形术。术语“预制”指通过在组织本身内植入血管蒂使组织新生血管化的过程;该组织可以通过蒂本身在短距离内重新植入,或者通过微血管吻合作为游离移植物。预制的目的是建立一个组织(肌肉、骨骼、皮肤或复合材料),其特征尽可能与缺损相似,从而最大限度地减少供体部位的发病率,提高重建效果。我们对文献进行了回顾,其中包括迄今为止进行的主要实验,其中使用支架和生长因子重建骨段,与局部血液供应或血管蒂的使用有关。
{"title":"Historical review of bone prefabrication.","authors":"Claudia Di Bella,&nbsp;Enrico Lucarelli,&nbsp;Davide Donati","doi":"10.1007/s12306-008-0052-5","DOIUrl":"https://doi.org/10.1007/s12306-008-0052-5","url":null,"abstract":"<p><p>Prefabricated tissue represents a bridge between traditional reconstructive surgery and tissue engineering. Initially used in the 1960s in reconstructive plastic surgery, in the 1980s it was also used in orthopedics. The term \"prefabricated\" indicates a process of neovascularization of a tissue by implanting a vascular pedicle inside the tissue itself; this tissue can be then reimplanted either at a short distance through the pedicle itself, or as a free graft by microvascular anastomosis. The purpose of prefabrication is to build a tissue (muscle, bone, skin, or composite) with characteristics as similar as possible to those of the defect to fill, thus minimizing morbidity in the donor site and improving the reconstructive effectiveness. We present a review of the literature that includes the main experiments performed until now in which a bone segment has been reconstructed using scaffolds and growth factors in relationship to the local blood supply or to the use of a vascular pedicle.</p>","PeriodicalId":76085,"journal":{"name":"La Chirurgia degli organi di movimento","volume":"92 2","pages":"73-8"},"PeriodicalIF":0.0,"publicationDate":"2008-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12306-008-0052-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27647370","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Isolated congenital absence of posterior cruciate ligament? A case report. 孤立性先天性后交叉韧带缺失?一份病例报告。
Pub Date : 2008-09-01 Epub Date: 2008-05-06 DOI: 10.1007/s12306-008-0044-5
Marco da Gama Malchér, Andrea A M Bruno, Benedetta Grisone, Giuseppina Bernardelli, Luca Pietrogrande

A rare case of a 28-year-old Asiatic male with the isolated absence of a posterior cruciate ligament is reported. Clinical features, diagnostic steps, therapeutic strategies and follow-up are described. A review of the literature is also presented.

一个罕见的情况下,一个28岁的亚洲男性孤立缺席后交叉韧带报告。临床特点,诊断步骤,治疗策略和随访描述。文献综述也提出。
{"title":"Isolated congenital absence of posterior cruciate ligament? A case report.","authors":"Marco da Gama Malchér,&nbsp;Andrea A M Bruno,&nbsp;Benedetta Grisone,&nbsp;Giuseppina Bernardelli,&nbsp;Luca Pietrogrande","doi":"10.1007/s12306-008-0044-5","DOIUrl":"https://doi.org/10.1007/s12306-008-0044-5","url":null,"abstract":"<p><p>A rare case of a 28-year-old Asiatic male with the isolated absence of a posterior cruciate ligament is reported. Clinical features, diagnostic steps, therapeutic strategies and follow-up are described. A review of the literature is also presented.</p>","PeriodicalId":76085,"journal":{"name":"La Chirurgia degli organi di movimento","volume":"92 2","pages":"105-7"},"PeriodicalIF":0.0,"publicationDate":"2008-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12306-008-0044-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27424691","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Asymmetrical bilateral traumatic fracture dislocation of the hip: a report of two cases. 不对称双侧外伤性髋骨折脱位2例报告。
Pub Date : 2008-09-01 Epub Date: 2008-05-26 DOI: 10.1007/s12306-008-0045-4
Raffaele Pascarella, Alessandra Maresca, Michele Cappuccio, Leonardo Marchesini Reggiani, Stefano Boriani

We report on two cases of simultaneous asymmetrical bilateral hip dislocation. Both patients were involved in car accidents. The first case is a 23-year-old man who had a bilateral hip dislocation, anterior on the right side and posterior on the left associated with bilateral femoral head fracture. The second case presented the same dislocations of the hips associated with acetabular fracture on the right side. Closed reduction of the hips was performed in both cases. In the first case the femoral head fragments was subsequently removed. In the second case internal fixation of the acetabular fracture was postponed.

我们报告两例同时不对称双侧髋关节脱位。两位病人都发生了车祸。第一个病例是一名23岁的男性,他患有双侧髋关节脱位,右侧前位,左侧后位并伴有双侧股骨头骨折。第二个病例出现相同的髋关节脱位并伴有右侧髋臼骨折。两例患者均行髋部闭合复位。第一例股骨头碎片随后被取出。第二例髋臼骨折内固定手术延期。
{"title":"Asymmetrical bilateral traumatic fracture dislocation of the hip: a report of two cases.","authors":"Raffaele Pascarella,&nbsp;Alessandra Maresca,&nbsp;Michele Cappuccio,&nbsp;Leonardo Marchesini Reggiani,&nbsp;Stefano Boriani","doi":"10.1007/s12306-008-0045-4","DOIUrl":"https://doi.org/10.1007/s12306-008-0045-4","url":null,"abstract":"<p><p>We report on two cases of simultaneous asymmetrical bilateral hip dislocation. Both patients were involved in car accidents. The first case is a 23-year-old man who had a bilateral hip dislocation, anterior on the right side and posterior on the left associated with bilateral femoral head fracture. The second case presented the same dislocations of the hips associated with acetabular fracture on the right side. Closed reduction of the hips was performed in both cases. In the first case the femoral head fragments was subsequently removed. In the second case internal fixation of the acetabular fracture was postponed.</p>","PeriodicalId":76085,"journal":{"name":"La Chirurgia degli organi di movimento","volume":"92 2","pages":"109-11"},"PeriodicalIF":0.0,"publicationDate":"2008-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12306-008-0045-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27462599","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 24
Isolation, characterisation and osteogenic potential of human bone marrow stromal cells derived from the medullary cavity of the femur. 来自股骨髓腔的人骨髓基质细胞的分离、表征和成骨潜能。
Pub Date : 2008-09-01 Epub Date: 2008-09-12 DOI: 10.1007/s12306-008-0057-0
Elisa Leonardi, Valentina Devescovi, Francesca Perut, Gabriela Ciapetti, Armando Giunti

Marrow stromal cells (MSC) are increasingly being introduced in orthopaedic practice as potentially powerful effectors of bone regeneration. Since cell recovery of MSC is affected by a high degree of individual variability, sources for collecting adequate amounts of safe and effective MSC under routine conditions are needed. We analysed if femoral bone marrow, which is usually discarded during total hip arthroplasty procedures, is a reliable source of MSC to enhance bone healing and regeneration. Mononuclear cells were isolated, assayed for typical MSC markers, harvested under appropriate culture conditions and evaluated for their ability to differentiate into osteoblasts. Cell recovery and osteogenic potential were independent from donor gender or age, suggesting that elderly individuals are eligible for autologous cell therapy. Although heterogeneous, the pool of MSC recovered from femoral marrow without further in vitro selection or manipulation proved highly effective in proliferating and differentiating along the osteogenic lineage. In conclusion, this source of MSC offers a valuable tool to be used to promote osteogenesis and implant fixation.

骨髓基质细胞(MSC)作为潜在的强大的骨再生效应器越来越多地被引入骨科实践。由于间充质干细胞的细胞恢复受到高度个体差异的影响,因此需要在常规条件下收集足够数量的安全有效的间充质干细胞。我们分析了在全髋关节置换术中通常被丢弃的股骨骨髓是否是一种可靠的间充质干细胞来源,以促进骨愈合和再生。分离单个核细胞,检测典型的MSC标记物,在适当的培养条件下收获,并评估其向成骨细胞分化的能力。细胞恢复和成骨潜能与供体性别或年龄无关,这表明老年人适合自体细胞治疗。尽管存在异质性,但未经进一步的体外选择或操作,从股骨骨髓中恢复的间充质干细胞池在沿成骨谱系增殖和分化方面证明是非常有效的。总之,这种来源的间充质干细胞提供了一种有价值的工具,用于促进成骨和植入物固定。
{"title":"Isolation, characterisation and osteogenic potential of human bone marrow stromal cells derived from the medullary cavity of the femur.","authors":"Elisa Leonardi,&nbsp;Valentina Devescovi,&nbsp;Francesca Perut,&nbsp;Gabriela Ciapetti,&nbsp;Armando Giunti","doi":"10.1007/s12306-008-0057-0","DOIUrl":"https://doi.org/10.1007/s12306-008-0057-0","url":null,"abstract":"<p><p>Marrow stromal cells (MSC) are increasingly being introduced in orthopaedic practice as potentially powerful effectors of bone regeneration. Since cell recovery of MSC is affected by a high degree of individual variability, sources for collecting adequate amounts of safe and effective MSC under routine conditions are needed. We analysed if femoral bone marrow, which is usually discarded during total hip arthroplasty procedures, is a reliable source of MSC to enhance bone healing and regeneration. Mononuclear cells were isolated, assayed for typical MSC markers, harvested under appropriate culture conditions and evaluated for their ability to differentiate into osteoblasts. Cell recovery and osteogenic potential were independent from donor gender or age, suggesting that elderly individuals are eligible for autologous cell therapy. Although heterogeneous, the pool of MSC recovered from femoral marrow without further in vitro selection or manipulation proved highly effective in proliferating and differentiating along the osteogenic lineage. In conclusion, this source of MSC offers a valuable tool to be used to promote osteogenesis and implant fixation.</p>","PeriodicalId":76085,"journal":{"name":"La Chirurgia degli organi di movimento","volume":"92 2","pages":"97-103"},"PeriodicalIF":0.0,"publicationDate":"2008-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12306-008-0057-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27674766","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 19
Freeman-Sheldon syndrome. A case report and review of the literature. Freeman-Sheldon综合症。病例报告及文献回顾。
Pub Date : 2008-09-01 Epub Date: 2008-08-01 DOI: 10.1007/s12306-008-0053-4
Daniele Ferrari, Camilla Bettuzzi, Onofrio Donzelli

The Authors describe a case of Freeman-Sheldon Syndrome, a rare congenital autosomal dominant disorder (gene mapped on chromosome 11p15.5) characterized by microstomia with crinkled lips, camptodactyly with ulnar deviation of the fingers and equinus-varus-supine clubfoot. The autosomal recessive form, even rarer and difficult to recognize, has a more severe clinical manifestation. The symptomatology is worsened by breathing and swallowing disorders due to the small orifices of the mouth and nose, which sometimes require tracheotomy to avoid obstruction of the airways.

作者描述了一例弗里曼-谢尔登综合征,这是一种罕见的先天性常染色体显性遗传病(基因定位在11p15.5染色体上),其特征是小口畸形伴嘴唇起皱,camptodacly伴手指尺侧偏差和马蹄-内翻-平卧畸形足。常染色体隐性型更为罕见且难以识别,其临床表现更为严重。由于口鼻小口导致呼吸和吞咽障碍,有时需要气管切开术以避免气道阻塞,从而使症状恶化。
{"title":"Freeman-Sheldon syndrome. A case report and review of the literature.","authors":"Daniele Ferrari,&nbsp;Camilla Bettuzzi,&nbsp;Onofrio Donzelli","doi":"10.1007/s12306-008-0053-4","DOIUrl":"https://doi.org/10.1007/s12306-008-0053-4","url":null,"abstract":"<p><p>The Authors describe a case of Freeman-Sheldon Syndrome, a rare congenital autosomal dominant disorder (gene mapped on chromosome 11p15.5) characterized by microstomia with crinkled lips, camptodactyly with ulnar deviation of the fingers and equinus-varus-supine clubfoot. The autosomal recessive form, even rarer and difficult to recognize, has a more severe clinical manifestation. The symptomatology is worsened by breathing and swallowing disorders due to the small orifices of the mouth and nose, which sometimes require tracheotomy to avoid obstruction of the airways.</p>","PeriodicalId":76085,"journal":{"name":"La Chirurgia degli organi di movimento","volume":"92 2","pages":"127-31"},"PeriodicalIF":0.0,"publicationDate":"2008-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12306-008-0053-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27576051","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
期刊
La Chirurgia degli organi di movimento
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
﹀
mjeditor
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1