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Diagnosis and treatment of posterior sternoclavicular joint dislocations in children. 儿童胸锁骨后关节脱位的诊断与治疗。
Pub Date : 1996-08-01 DOI: 10.1097/01241398-199701000-00068
J. Yang, H. al-Etani, M. Letts
Posterior dislocation of the sternoclavicular joint is uncommon in children, difficult to diagnose, and may be confused with a physical injury of the medial clavicle. We reviewed our experience with posterior dislocations of the medial clavicle over a 10-year period, and found 5 children who had sustained this injury. The computed tomography (CT) scan was found to be the best diagnostic procedure to assess the integrity of the sternoclavicular joint. The cause of the dislocation was most commonly lateral compression of the shoulders sustained during contact sports, particularly football and hockey. Reduction was usually obtained by retraction of the shoulders; for persistent dislocations, a towel clip was used to lift the medial end of the clavicle into its reduced position with the patient under general anesthesia. Reduction was maintained with a figure-of-eight bandage. Any child presenting with pain and swelling in the region of the sternoclavicular joint and no evidence of obvious fracture of the clavicle should have the possibility of dislocation of the sternoclavicular joint investigated with a CT scan.
胸锁关节后路脱位在儿童中并不常见,难以诊断,并可能与内侧锁骨的物理损伤混淆。我们回顾了10年来治疗内侧锁骨后脱位的经验,发现5名儿童遭受了这种损伤。计算机断层扫描(CT)被认为是评估胸锁关节完整性的最佳诊断程序。脱位最常见的原因是在身体接触运动中,特别是足球和曲棍球运动中持续的肩部侧向压迫。复位通常通过肩部内收获得;对于持续脱位的患者,在全身麻醉下使用毛巾夹将锁骨内侧端抬至复位位置。复位用八字形绷带维持。任何表现为胸锁关节区域疼痛和肿胀且无明显锁骨骨折迹象的儿童,应通过CT扫描调查胸锁关节脱位的可能性。
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引用次数: 36
Pectoralis tendon avulsion in the skeletally immature. 胸肌肌腱撕脱在骨骼未成熟。
Pub Date : 1996-08-01 DOI: 10.1097/01241398-199701000-00071
P. Simonian, M. E. Morris
Pectoralis tendon avulsion is a rare injury typically occurring in skeletally mature men. The diagnosis can be difficult to make and is often delayed. We report a case of a complete bony avulsion of the pectoralis tendon at the site of its humeral insertion in a skeletally immature male. The palpable and radiographic evidence of ossification at the injury site made the diagnosis in this adolescent case uniquely obvious.
胸肌肌腱撕脱伤是一种罕见的损伤,通常发生在骨骼成熟的男性。诊断可能很难做出,而且往往被延误。我们报告一个完整的骨撕脱的胸肌肌腱在其肱骨插入的地方在一个骨骼未成熟的男性。损伤部位骨化的可触及和影像学证据使得这个青少年病例的诊断非常明显。
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引用次数: 15
Triplane fracture associated with a proximal third fibula fracture. 三平面骨折合并第三腓骨近端骨折。
Pub Date : 1996-06-01 DOI: 10.1097/01241398-199701000-00073
W. Healy, K. Starkweather, J. Meyer, G. A. Teplitz
The case of a Maisonneuve fracture occurring in association with a triplane fracture in an adolescent wrestler is presented. In this combination of injuries, the deltoid ligament may be ruptured, and/or the medial malleolus fractured. If the proximal fibula fracture is not discovered, and the syndesmosis rupture is not treated, the resulting chronic talocrural instability may lead to chronic ankle pain and degenerative arthritis. The orthopedist should be aware of the possibility of a Maisonneuve fracture occurring in association with a triplane fracture, and should treat both injuries appropriately.
一例Maisonneuve骨折发生与三面骨折的青少年摔跤运动员提出。在这种组合损伤中,三角韧带可能断裂,和/或内踝骨折。如果腓骨近端骨折未被发现,并且联合破裂未得到治疗,则由此产生的慢性距骨不稳定可能导致慢性踝关节疼痛和退行性关节炎。骨科医生应意识到Maisonneuve骨折合并三面骨折的可能性,并应适当治疗两种损伤。
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引用次数: 19
Ultrasonography in the management of painful hips in children. 超声检查在治疗儿童髋关节疼痛中的应用。
Pub Date : 1996-06-01 DOI: 10.1097/01241398-199701000-00044
P. Nimityongskul, A. McBryde, L. Anderson, J. Crotty
The decision to aspirate a painful hip joint is often based on history, physical, and laboratory findings. The purpose of this study is to determine whether ultrasound is helpful in making decisions to aspirate a painful hip joint in children. The anterior capsular distance was determined in 10 children with painful or irritable hips. This anterior capsular distance is 2 to 4 mm in most hips. A side difference of 2 mm or more is considered a significant capsular distension. Based on these criteria and clinical parameters, 3 hips were aspirated, and 7 were observed without aspiration. None of the 7 hips subsequently required further diagnostic workup or treatment and all have had a satisfactory outcome. Ultrasound is a reliable method to detect capsular distension or joint effusion. It helps significantly in making the decision as to "when to aspirate" a painful or irritable hip joint.
髋关节疼痛的抽吸决定通常基于病史、生理和实验室结果。本研究的目的是确定超声是否有助于儿童髋关节疼痛的抽吸决定。对10例髋部疼痛或易激儿童进行前囊距离测定。在大多数髋部,前囊距离为2 - 4mm。2毫米或以上的侧差被认为是明显的囊膜膨胀。根据这些标准和临床参数,3髋被抽吸,7髋未被抽吸。这7个髋关节随后都不需要进一步的诊断检查或治疗,所有的结果都令人满意。超声是检测关节囊膨胀或关节积液的可靠方法。当髋关节疼痛或易激时,它在决定“何时吸气”方面有很大的帮助。
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引用次数: 8
Pyogenic infectious spondylitis in children. The evolution to current thought. 儿童化脓性感染性脊柱炎。进化到现在的思想。
Pub Date : 1996-05-01 DOI: 10.1097/01241398-199611000-00047
David Ring, D. Wenger
The historic evolution of pyogenic infectious spondylitis from its initial descriptions to its current characterization illustrates the degree to which our means of perception and evaluation influence our understanding of an illness. As new concepts resulting from medical innovations challenge traditional beliefs regarding the etiology and optimum treatment of pyogenic infectious spondylitis in children (commonly termed discitis), controversies have arisen. This review attempts to clarify these issues by reconstructing their historic basis and delineating the limitations of our current knowledge. In our opinion, this exercise demonstrates the similarities between pyogenic infectious spondylitis in children and adults and provides support for the management of this illness at all ages with parenteral antibiotics, cast or brace immobilization when needed for symptomatic relief, and, rarely, operative débridement.
化脓性感染性脊柱炎从最初的描述到目前的特征,其历史演变说明了我们的感知和评估方式影响我们对疾病理解的程度。由于医学创新产生的新概念挑战了关于儿童化脓性感染性脊柱炎(通常称为椎间盘炎)的病因和最佳治疗的传统观念,因此出现了争议。这篇综述试图通过重建它们的历史基础和描述我们目前知识的局限性来澄清这些问题。在我们看来,这项研究显示了儿童和成人化脓性感染性脊柱炎的相似之处,并为所有年龄段的这种疾病的治疗提供了支持,在需要缓解症状时使用肠外抗生素、石膏或支具固定,很少使用手术治疗。
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引用次数: 18
Resolving neonatal osteochondroma: a case report and literature review. 新生儿骨软骨瘤的治疗:1例报告并文献复习。
Pub Date : 1996-03-01 DOI: 10.1097/00004694-199609000-00087
Shaw Ba
We report a case of spontaneous resolution of a congenital osteochondroma in a child with metachondromatosis. We could find no reports of congenital or neonatal osteochondromas. Furthermore, reports of spontaneous resolution of osteochondromas are rare. We conclude that some of these radiologically benign lesions may be observed in very young patients.
我们报告一例自发性解决先天性骨软骨瘤在一个孩子与异软骨瘤病。我们没有发现先天性或新生儿骨软骨瘤的报告。此外,骨软骨瘤自发消退的报道是罕见的。我们的结论是,这些放射学上的良性病变可以在非常年轻的患者中观察到。
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引用次数: 5
The acquisition of knowledge. 获取知识。
Pub Date : 1996-01-01 DOI: 10.1007/978-1-4419-1428-6_3046
D. Rumbaugh, James E. King, M. Beran, D. Washburn, K. Gould, Nate Kornell, D. J. Scaturo, B. Haig, R. Schvaneveldt, B. Barton, T. Ulrich, Peter Robinson, Matthew J. Schuelke, E. Day, Henry W. Chase, E. Carayannis, Timothy M. Flemming, M. Mitchelmore, Paul White, Erin M. Brodhagen, M. Gettinger, E. Usher, D. B. Morris, Janna Wardman, J. R. Nelson, R. Low, P. Jin, Betty K. Tuller, N. Nguyen, Fons Wijnhoven, G. Weber, C. Rigg, K. Trehan, Michael L. Jones, Aytac Gogus, N. Seel, S. Naidu, Danny R. Bedgood, Christina M. Steiner, Birgit Marte, J. Heller, D. Albert, A. Podolskiy, L. Uden, Andrew J. Martin, C. Balkenius, B. Johansson, Karen L. Hollis, David A. Cook, J. Bloomberg, O. Bock, R. Clariana, Simon Hooper, Amy B. Adcock, R. Van Eck, C. Tsai, Chung-Yuan Hsu, M. Burtsev, J. S. Nairne, Marco Vasconcelos, Josefa N. S. Pandeirada, Liu Yang, J. Carbonell, M. Dornisch, G. Manaster, Katie Davis, Marcia L. Conner, Dolores Fidishun, M. Tennant, J. Gurlitt, J. Fletcher, S. Cerri, G. Veletsianos, P. Wickman, J. D. Ba
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引用次数: 118
Resolving neonatal osteochondroma: a case report and literature review. 新生儿骨软骨瘤的治疗:1例报告并文献复习。
Pub Date : 1996-01-01 DOI: 10.1097/01241398-199609000-00087
B. Shaw
We report a case of spontaneous resolution of a congenital osteochondroma in a child with metachondromatosis. We could find no reports of congenital or neonatal osteochondromas. Furthermore, reports of spontaneous resolution of osteochondromas are rare. We conclude that some of these radiologically benign lesions may be observed in very young patients.
我们报告一例自发性解决先天性骨软骨瘤在一个孩子与异软骨瘤病。我们没有发现先天性或新生儿骨软骨瘤的报告。此外,骨软骨瘤自发消退的报道是罕见的。我们的结论是,这些放射学上的良性病变可以在非常年轻的患者中观察到。
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引用次数: 6
Idiopathic juvenile osteoporosis. An unusual cause of back pain in an adolescent. 特发性青少年骨质疏松症。青少年背部疼痛的不寻常原因。
Pub Date : 1995-11-01 DOI: 10.1097/01241398-199605000-00038
J. Dimar, M. Campbell, S. Glassman, R. Puno, J. R. Johnson
Idiopathic juvenile osteoporosis represents a rare bone disorder that affects prepubescent children of both sexes. The diagnosis is generally one of exclusion, ruling out other potential metabolic bone diseases. Here, the authors present a representative case of this rare disorder in an otherwise healthy male, along with the clinical history, physical presentation, and review of the available literature. Finally, it is important to note that patients with this disorder often have profound involvement of the spinal column with multiple compression fractures.
特发性青少年骨质疏松症是一种罕见的影响青春期前男女儿童的骨骼疾病。诊断一般是一种排除,排除其他潜在的代谢性骨病。在这里,作者提出了一个具有代表性的病例,这种罕见的疾病,在其他方面健康的男性,随着临床病史,物理表现,并回顾现有的文献。最后,需要注意的是,患有这种疾病的患者通常深度累及脊柱并伴有多处压缩性骨折。
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引用次数: 5
The joy of teaching. 教学的乐趣。
Pub Date : 1995-10-01 DOI: 10.12968/sece.2018.15.8
Greer Rb rd
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引用次数: 17
期刊
American journal of orthopedics
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