Surgical Hip Dislocation
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H20/1, H20/2, H20/3, H20/4 (1000285 1000286 1000287 1000288) Latin
…going one step further H20/1 (1000285) H20/2 (1000286) H20/3 (1000287) H20/4 (1000288) H20/1, H20/2, H20/3, H20/4 (1000285_1000286_1000287_1000288) Latin H20/1, H20/2, H20/3, H20/4 H20/2, H20/3, H20/4 H20/4 1 Promontorium 38 Lig. longitudinale anterius 78 A. iliaca externa 2 Processus articularis 39 Membrana obturatoria 79 V. iliaca externa superior 40 Lig. sacrospinale 80 A. iliaca interna 3 Vertebra lumbalis V 41 Lig. sacrotuberale 81 V. iliaca interna 4 Processus costalis 42 Lig. inguinale 82 A. iliaca communis dextra 5 Discus intervertebralis 43 Ligg. sacroiliaca anteriora 83 V. cava inferior 6 Crista iliaca 44 Lig. iliolumbale 84 Pars abdominalis aortae 7 Ala ossis ilii 45 Ligg. sacroiliaca interossea 85 A. iliaca communis sinistra 8 Spina iliaca anterior 46 Lig. sacroiliacum posterius 86 N. ischiadicus superior 47 Lig. supraspinale 87 A. femoralis 9 Spina iliaca anterior 88 Plexus sacralis inferior 89 N. dorsalis clitoridis 10 Acetabulum H20/3, H20/4 90 N. pudendus 11 Foramen obturatum 48 Rectum 91 M. piriformis 12 Ramus ossis ischii 49 Ovarium 92 Nn. rectales inferiores 13 Ramus superior ossis pubis 50 Tuba uterina 93 Nn. perineales 14 Ramus inferior ossis pubis 51 Uterus 94 Nn. labiales posteriores 15 Tuberculum pubicum 52 Lig. ovarii proprium 95 V. femoralis 16 Crista pubica 53 Vesica urinaria 96 V. iliaca communis sinistra 17 Symphysis pubica 54 Membrana perinei 97 A. glutealis superior 18 Corpus ossis pubis 55 M. obturatorius internus 98 A. glutealis inferior 19 Tuber ischiadicum 56 M. transversus perinei 99 A. pudenda interna 20 Spina ischiadica profundus 100 ® A. -
Cerebral Palsy with Dislocated Hip and Scoliosis: What to Deal with First?
Current Concepts Review Cerebral palsy with dislocated hip and scoliosis: what to deal with first? Ilkka J. Helenius1 Cite this article: Helenius IJ, Viehweger E, Castelein RM. Cer- Elke Viehweger2 ebral palsy with dislocated hip and scoliosis: what to deal Rene M. Castelein3 with first?J Child Orthop 2020;14: 24-29. DOI: 10.1302/1863- 2548.14.190099 Abstract Keywords: cerebral palsy; hip dislocation; neuromuscular Purpose Hip dislocation and scoliosis are common in children scoliosis; CP surveillance; hip reconstruction; spinal fusion with cerebral palsy (CP). Hip dislocation develops in 15% and surgery 20% of children with CP, mainly between three and six years of age and especially in the spastic and dyskinetic subtypes. The risk of scoliosis increases with age and increasing disabili- Introduction ty as expressed by the Gross Motor Function Score. Hip dislocation develops in 15% and 20% of children with Methods A hip surveillance programme and early surgical cerebral palsy (CP), mainly between three and six years 1 treatment have been shown to reduce the hip dislocation, of age, and especially in the spastic dyskinetic subtypes. but it remains unclear if a similar programme could reduce Children with Gross Motor Function Classification System the need for neuromuscular scoliosis. When hip dislocation (GMFCS) level V demonstrate an incidence of hip dis- 2 and neuromuscular scoliosis are co-existent, there appears to placement up to 90%. The risk of scoliosis increases with 3 be no clear guidelines as to which of these deformities should age and increasing disability (increasing GMFCS level). be addressed first: hip or spine. The risk of scoliosis is 1% for GMFCS level I at ten years of age and 5% at 20 years, but 30% for GMFCS V at ten Results Hip dislocation or windswept deformity may cause years and 80% at 20 years. -
Spondylolisthesis, with Description of a Case
[Reprinted from the Transactions of the American Orthopedic Association, 1897.] SPONDYLOLISTHESIS, WITH DESCRIPTION OP A CASE. ROBERT W. LOVETT, M.D., BOSTON. The name spondylolisthesis (ottovoo/loc, a vertebra, and bhadrjat c, a gliding) refers to a forward subluxation of the body of one of the lower lumbar vertebrae, with the exception of one recorded case where the upper part of the sacrum was displaced forward. This displacement has ordinarily been described as a dislocation ; in most instances it hardly reaches a greater degree than may be described by the name subluxation. Even this name is incorrect anatomic- ally. This is because the body of the vertebra is chiefly affected, while the laminae and spinous process remain practically in place. The condition has attracted attention chiefly from the obstetrical point of view, on account of the secondary pelvic changes produced, and surgical literature contains next to nothing about it. Fr. Neugebauer, 1 of Warsaw, has so thoroughly investigated and elab- orated the subject that whoever strives to elucidate it from any point of view must do so largely by quotations from his extensive writings. In 1854, when this condition was recognized and named by Killian, 2 there were described only four known anatomical speci- mens. In 1890, when Neugebauer’s treatise was written, there were one hundred and one clinical and anatomical observations. Blake, 3 Gibuey, 4 and Lombard 5 contributed the only recorded American observations. Between the publication of Neugebauer’s classic in 1892, which was written in 1890, and to-day there have been reported, so far as I could find, twenty-four more cases (two in men). -
Treatment and Outcomes of Arthrogryposis in the Lower Extremity
Received: 25 June 2019 Revised: 31 July 2019 Accepted: 1 August 2019 DOI: 10.1002/ajmg.c.31734 RESEARCH ARTICLE Treatment and outcomes of arthrogryposis in the lower extremity Reggie C. Hamdy1,2 | Harold van Bosse3 | Haluk Altiok4 | Khaled Abu-Dalu5 | Pavel Kotlarsky5 | Alicja Fafara6,7 | Mark Eidelman5 1Shriners Hospitals for Children, Montreal, Québec, Canada Abstract 2Department of Pediatric Orthopaedic In this multiauthored article, the management of lower limb deformities in children Surgery, Faculty of Medicine, McGill with arthrogryposis (specifically Amyoplasia) is discussed. Separate sections address University, Montreal, Québec, Canada 3Shriners Hospitals for Children, Philadelphia, various hip, knee, foot, and ankle issues as well as orthotic treatment and functional Pennsylvania outcomes. The importance of very early and aggressive management of these defor- 4 Shriners Hospitals for Children, Chicago, mities in the form of intensive physiotherapy (with its various modalities) and bracing Illinois is emphasized. Surgical techniques commonly used in the management of these con- 5Pediatric Orthopedics, Technion Faculty of Medicine, Ruth Children's Hospital, Haifa, ditions are outlined. The central role of a multidisciplinary approach involving all Israel stakeholders, especially the families, is also discussed. Furthermore, the key role of 6Faculty of Health Science, Institute of Physiotherapy, Jagiellonian University Medical functional outcome tools, specifically patient reported outcomes, in the continuous College, Krakow, Poland monitoring and evaluation of these deformities is addressed. Children with 7 Arthrogryposis Treatment Centre, University arthrogryposis present multiple problems that necessitate a multidisciplinary Children's Hospital, Krakow, Poland approach. Specific guidelines are necessary in order to inform patients, families, and Correspondence health care givers on the best approach to address these complex conditions Reggie C. -
Periacetabular Osteotomy (PAO) of the Hip
UW HEALTH SPORTS REHABILITATION Rehabilitation Guidelines For Periacetabular Osteotomy (PAO) Of The Hip The hip joint is composed of the femur (the thigh bone) and the Lunate surface of acetabulum acetabulum (the socket formed Articular cartilage by the three pelvic bones). The Anterior superior iliac spine hip joint is a ball and socket joint Head of femur Anterior inferior iliac spine that not only allows flexion and extension, but also rotation of the Iliopubic eminence Acetabular labrum thigh and leg (Fig 1). The head of Greater trochanter (fibrocartilainous) the femur is encased by the bony Fat in acetabular fossa socket in addition to a strong, (covered by synovial) Neck of femur non-compliant joint capsule, Obturator artery making the hip an extremely Anterior branch of stable joint. Because the hip is Intertrochanteric line obturator artery responsible for transmitting the Posterior branch of weight of the upper body to the obturator artery lower extremities and the forces of Obturator membrane Ischial tuberosity weight bearing from the foot back Round ligament Acetabular artery up through the pelvis, the joint (ligamentum capitis) Lesser trochanter Transverse is subjected to substantial forces acetabular ligament (Fig 2). Walking transmits 1.3 to Figure 1 Hip joint (opened) lateral view 5.8 times body weight through the joint and running and jumping can generate forces across the joint fully form, the result can be hip that is shared by the whole hip, equal to 6 to 8 times body weight. dysplasia. This causes the hip joint including joint surfaces and the to experience load that is poorly previously-mentioned acetabular The labrum is a circular, tolerated over time, resulting in labrum. -
The Orthopaedic Management of Arthrogryposis Multiplex Congenita
Current Concept Review The Orthopaedic Management of Arthrogryposis Multiplex Congenita Harold J. P. van Bosse, MD and Dan A. Zlotolow, MD Shriners Hospital for Children, Philadelphia, PA Abstract: Arthrogryposis multiplex congenita (AMC) describes a baby born with multiple joint contractures that results from fetal akinesia with at least 400 different causes. The most common forms of AMC are amyoplasia (classic ar- throgryposis) and the distal arthrogryposes. Over the past two decades, the orthopaedic treatment of children with AMC has evolved with a better appreciation of the natural history. Most adults with arthrogryposis are ambulatory, but less than half are fully independent in self-care and most are limited by upper extremity dysfunction. Chronic and epi- sodic pain in adulthood—particularly of the foot and back—is frequent, limiting both ambulation and standing. To improve upon the natural history, upper extremity treatments have advanced to improve elbow motion and wrist and thumb positioning. Attempts to improve the ambulatory ability and decrease future pain include correction of hip and knee contractures and emphasizing casting treatments of foot deformities. Pediatric patients with arthrogryposis re- quire a careful evaluation, with both a physical examination and an assessment of needs to direct their treatment. Fur- ther outcomes studies are needed to continue to refine procedures and define the appropriate candidates. Key Concepts: • Arthrogryposis multiplex congenita (AMC) is a term that describes a baby born with multiple joint contractures. Amyoplasia is the most common form of AMC, accounting for one-third to one-half of all cases, with the distal arthrogryposes as the second largest AMC type. -
Spinopelvic Mobility As It Relates to Total Hip Arthroplasty Cup Positioning: a Case Report and Review of the Literature
REVIEW Spinopelvic Mobility as it Relates to Total Hip Arthroplasty Cup Positioning: A Case Report and Review of the Literature ABSTRACT Alexander M. Crawford, MD1 Hip-spine syndrome occurs when arthroses of the hip and spine coexist. Patrick K. Cronin, MD1 Hip-spine syndrome can result in abnormal spinopelvic mobility, which is Jeffrey K. Lange, MD2 becoming increasingly recognized as a cause of dislocation following total James D. Kang, MD3 hip arthroplasty (THA). The purpose of this article is to summarize the cur- rent understanding of normal and abnormal spinopelvic mobility as it re- lates to THA component positioning and to provide actionable recommen- dations to prevent spinopelvic mobility-related dislocations. In so doing, we also provide a recommended workup and case-example of a patient AUTHOR AFFILIATIONS with abnormal spinopelvic mobility. 1Harvard Combined Orthopaedic Residency Program, Harvard Medical LEVEL OF EVIDENCE Level V Narrative Review School, Boston, MA 2Department of Adult Reconstruction and Total Joint Arthroplasty, Brigham KEYWORDS Spinopelvic mobility, hip-spine syndrome, fixed sagittal plane and Women’s Hospital, Boston, MA imbalance, total hip arthroplasty 3Department of Orthopaedic Spine Surgery, Brigham and Women’s Hospital, Boston, MA Dislocation following total hip arthroplasty (THA) causes significant morbidity for pa- CORRESPONDING AUTHOR tients, and accounts for approximately 17% of all revision hip replacement surgeries.1 THA Alex Crawford, MD instability can have multiple causes, including component malposition, soft tissue imbal- Massachusetts General Hospital ance, impingement, and late wear.2 Acetabular component positioning has been one major Department of Orthopaedic Surgery consideration historically for optimizing construct stability. The classic ‘safe zone’ for cup 55 Fruit St, White 535 position described by Lewinneck et al. -
Physical Assessment of the Newborn: Part 3
Physical Assessment of the Newborn: Part 3 ® Evaluate facial symmetry and features Glabella Nasal bridge Inner canthus Outer canthus Nasal alae (or Nare) Columella Philtrum Vermillion border of lip © K. Karlsen 2013 © K. Karlsen 2013 Forceps Marks Assess for symmetry when crying . Asymmetry cranial nerve injury Extent of injury . Eye involvement ophthalmology evaluation © David A. ClarkMD © David A. ClarkMD © K. Karlsen 2013 © K. Karlsen 2013 The S.T.A.B.L.E® Program © 2013. Handout may be reproduced for educational purposes. 1 Physical Assessment of the Newborn: Part 3 Bruising Moebius Syndrome Congenital facial paralysis 7th cranial nerve (facial) commonly Face presentation involved delivery . Affects facial expression, sense of taste, salivary and lacrimal gland innervation Other cranial nerves may also be © David A. ClarkMD involved © David A. ClarkMD . 5th (trigeminal – muscles of mastication) . 6th (eye movement) . 8th (balance, movement, hearing) © K. Karlsen 2013 © K. Karlsen 2013 Position, Size, Distance Outer canthal distance Position, Size, Distance Outer canthal distance Normal eye spacing Normal eye spacing inner canthal distance = inner canthal distance = palpebral fissure length Inner canthal distance palpebral fissure length Inner canthal distance Interpupillary distance (midpoints of pupils) distance of eyes from each other Interpupillary distance Palpebral fissure length (size of eye) Palpebral fissure length (size of eye) © K. Karlsen 2013 © K. Karlsen 2013 Position, Size, Distance Outer canthal distance -
Short Stature, Platyspondyly, Hip Dysplasia, and Retinal
CORE Metadata, citation and similar papers at core.ac.uk Provided by Springer - Publisher Connector Sangsin et al. BMC Medical Genetics (2016) 17:96 DOI 10.1186/s12881-016-0357-4 CASE REPORT Open Access Short stature, platyspondyly, hip dysplasia, and retinal detachment: an atypical type II collagenopathy caused by a novel mutation in the C-propeptide region of COL2A1: a case report Apiruk Sangsin1,2,3,4, Chalurmpon Srichomthong1,2, Monnat Pongpanich5,6, Kanya Suphapeetiporn1,2,7* and Vorasuk Shotelersuk1,2 Abstract Background: Heterozygous mutations in COL2A1 create a spectrum of clinical entities called type II collagenopathies that range from in utero lethal to relatively mild conditions which become apparent only during adulthood. We aimed to characterize the clinical, radiological, and molecular features of a family with an atypical type II collagenopathy. Case presentation: A family with three affected males in three generations was described. Prominent clinical findings included short stature with platyspondyly, flat midface and Pierre Robin sequence, severe dysplasia of the proximal femora, and severe retinopathy that could lead to blindness. By whole exome sequencing, a novel heterozygous deletion, c.4161_4165del, in COL2A1 was identified. The phenotype is atypical for those described for mutations in the C-propeptide region of COL2A1. Conclusions: We have described an atypical type II collagenopathy caused by a novel out-of-frame deletion in the C-propeptide region of COL2A1. Of all the reported truncating mutations in the C-propeptide region that result in short-stature type II collagenopathies, this mutation is the farthest from the C-terminal of COL2A1. Keywords: COL2A1, C-propeptide region, Exome sequencing, Type II collagenopathies Background mutations in the triple-helical or N-propeptide regions, Patients with COL2A1 mutations are collectively called those in the C-propeptide region generally produce atypical type II collagenopathies. -
Anatomic Study of Innervation of the Anterior Hip Capsule: Implication
Regional Anesthesia & Pain Medicine: first published as 10.1097/AAP.0000000000000701 on 1 February 2018. Downloaded from CHRONIC AND INTERVENTIONAL PAIN ORIGINAL ARTICLE Anatomic Study of Innervation of the Anterior Hip Capsule Implication for Image-Guided Intervention Anthony J. Short, MBBS,* Jessi Jo G. Barnett,† Michael Gofeld, MD,‡ Ehtesham Baig, MD,‡ KarenLam,MD,‡ Anne M.R. Agur, PhD,† and Philip W.H. Peng, MBBS, FRCPC, Founder (Pain Medicine)‡§ develop painful hip OA by the age of 85 years.1 The management Background and Objectives: The purpose of this cadaveric study was strategies consist of pharmacologic treatments, physical therapy, to determine the pattern of anterior hip capsule innervation and the associ- interventional techniques, and surgery.2 Total hip arthroplasty is ated bony landmarks for image-guided radiofrequency denervation. considered for patients with advanced OA and moderate to severe Methods: Thirteen hemipelvises were dissected to identify innervation of symptoms.3 New, noninvasive treatment options need to be devel- the anterior hip capsule. The femoral (FN), obturator (ON), and accessory oped for patients who cannot undergo surgery and for those with obturator (AON) nerves were traced distally, and branches supplying the severe postoperative pain. Radiofrequency denervation (RFD), anterior capsule documented. The relationships of the branches to bony known to be effective for facet and sacroiliac joint arthritis,4 is landmarks potentially visible with ultrasound were identified. now emerging as a possible treatment for chronic hip pain. In a re- Results: The anterior hip capsule received innervation from the FNs and view article, Gupta et al5 described 8 case reports/case series ONs in all specimens and the AON in 7 of 13 specimens. -
Tragelaphus Spekii
ORIGINAL COMMUNICATION Anatomy Journal of Africa. 2021. Vol 10 (1):1974-1979 GROSS ANATOMICAL STUDIES ON THE HIND LIMB OF THE SITATUNGA (Tragelaphus spekii). Kenechukwu Tobechukwu Onwuama, Sulaiman Olawoye Salami, Esther Solomon Kigir, Alhaji Zubair Jaji Department of Veterinary Anatomy, University of Ilorin, Ilorin, Nigeria Abbreviated title: Hind limb bones of the Sitatunga Corresponding address: Kenechukwu Tobechukwu Onwuama. Telephone number: 08036425961. E-mail address: [email protected] ABSTRACT The Sitatunga, Tragelaphus spekii, is a swamp dwelling antelope resident in West Africa. This study was carried out to document unique morphological and numerical information on the hind limb bones of this ruminant. Two (2) adults of both sexes were obtained as carcass at different times after post-mortem examination and prepared to extract the bones via cold water maceration for use in the study. The presence of a sharp pointed ilio-pubic eminence at the junction between the cranial border of the ilium and pubis; less prominent ischial tuber, inconspicuous ischiatic arch and a large oval obturator foramen were unique features of the Ossa coxarum that distinguished it from that of small ruminants. The Femur’s medial condyle was obliquely orientated, the fibula was absent while the long Tibia was typical of ruminant presentation. It was observed that the morphological features of the tarsals and Pes were also typical. However, the last Phalanges presented characteristic long triangular shaped bones with sharp pointed ends. The total number of bones making up the forelimb was accounted to be 45. In conclusion, this study has provided a baseline data for further biological, archeological and comparative anatomical studies. -
Congenital Hip Dislocation
Congenital Hip Dislocation What is a congenital hip dislocation? A congenital hip dislocation is an abnormal formation of the hip joint that is present at birth. Children with congenital hip dislocations may have instability of the hip, since the femoral head (top of the femur, or thighbone) does not fit tightly into the acetabulum (socket). The ligaments of the hip joint may also be loose. Children with congenital hip dislocation may have legs of different lengths and/or decreased movement on one leg. Congenital hip dislocation Normal hip Dislocated hip Femoral head out of Acetabulum acetabulum Femur Diagrams courtesy of the National Library of Medicine What causes congenital hip dislocation? The exact cause of congenital hip dislocation is not known. Some families have been reported to have a hereditary form of congenital hip dislocation (meaning multiple family members are affected). Congenital hip dislocation is more common in girls and babies born in the breech position (feet first); the left hip is also more often involved than the right hip. How is congenital hip dislocation treated? Shortly after birth, babies with congenital hip dislocation may be fitted with a device to help hold the hip in place. Surgery may be necessary if the dislocation is diagnosed at an older age or if earlier treatment options did not work. Left untreated, congenital hip dislocation may lead to problems with walking or activity, as well as pain and arthritis (inflammation of the hip joint) by early adulthood. Your child’s doctor(s) will discuss appropriate treatment options with you. For more information About.com ADAM Healthcare Center - http://adam.about.com/encyclopedia/infectiousdiseases/Developmental-dysplasia-of-the-hip.htm MedlinePlus Medical Encyclopedia - http://www.nlm.nih.gov/medlineplus/ency/article/000971.htm Source: About.com ADAM Healthcare Center .