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1.
J Pediatr Orthop ; 38(6): 305-311, 2018 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27328120

RESUMO

BACKGROUND: This study aimed to report the radiographic presentation of involved hips in children with hereditary multiple exostoses (HME). This included radiographic hip measurements, osteochondromas location, and relationship with hip subluxation. METHODS: Anteroposterior pelvis radiographs of children with HME, seen between 2003 and 2014, were retrospectively reviewed. Only patients who were skeletally immature at the first visit were included. One radiograph per patient per year was reviewed. Radiographs were examined for the presence of osteochondromas and their locations. Different parameters were evaluated: femoral neck-shaft angle, Reimer migration percentage (MP), Sharp acetabular angle, Wiberg angle, femoral head-neck ratio (coronal plane), and Shenton line. All measured radiographs were divided into 3 age groups:≤8,>8 and <13, and ≥13 years. Differences of the measured parameters with age were evaluated. Children with hip subluxation were identified and any relationship with osteochondromas locations, as well as MP changes over time, was recorded. Radiographs of children with a minimum 2-year follow-up were identified and changes of their hip measurements and osteochondromas' presence over time were recorded. RESULTS: A total of 51 children (102 hips) with HME were identified. In most locations, there was an overall increase of the occurrence of osteochondromas in the older age groups. However, in the medial femoral neck, a significantly less numbers of osteochondromas were found after 13 years of age (P=0.018). There was a decrease in MP with age (P<0.05). There was also an increase in Sharp and Wiberg angles in the older patients (P<0.05). Hips with broken Shenton line decreased in number with age (P 0.028). Hip subluxation was encountered in 23 hips. No specific location of osteochondromas was found to have a relationship with subluxation. Thirty-six children had a minimum follow-up of 2 years (mean age at first visit 8.5 y and at last visit 13.1 y). In these children, an increased occurrence of lesions was found in medial femoral neck and ischium (P<0.05) between the first and the last visit. CONCLUSIONS: In children with HME, radiographic evaluation of the hip is necessary based on the high percentage of hip involvement. When hip osteochondromas are found, radiographic surveillance is recommended to detect hip subluxation. Surgery may certainly be necessary for symptomatic osteochondromas. However, given the possibility of improvement in hip parameters with age, early surgical treatment to improve hip longevity does not seem to be warranted. LEVEL OF EVIDENCE: Level IV-prognostic study.


Assuntos
Exostose Múltipla Hereditária/diagnóstico por imagem , Luxação do Quadril/diagnóstico por imagem , Articulação do Quadril/diagnóstico por imagem , Acetábulo , Adolescente , Criança , Pré-Escolar , Exostose Múltipla Hereditária/epidemiologia , Feminino , Fêmur , Cabeça do Fêmur , Colo do Fêmur , Luxação do Quadril/epidemiologia , Humanos , Masculino , Osteocondroma , Radiografia , Estudos Retrospectivos
2.
J Pediatr Orthop ; 38(5): 266-273, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-27328121

RESUMO

BACKGROUND: Patellofemoral instability (PFI) has been the most reported knee abnormality in people with Down syndrome. Other reported knee abnormalities have been associated with PFI and different management approaches have been described with variable outcomes. The aim of this study was to describe the anatomic variations of the knee in children with Down syndrome. A comparison between knees with and without PFI was performed and our experience in treating knee abnormalities in Down syndrome was also reported. METHODS: Records of all children with Down syndrome were reviewed. Two groups were identified (knees with and without PFI). Radiographic measurements included the mechanical and anatomic lateral distal femoral angles, medial proximal tibial angle, angle of depression of medial tibial plateau, lateral tibial translation, and distal femoral physis-joint angle. On the lateral view, Insall-Salvati and Blackburne-Peel ratios were measured. The sulcus angle was measured on the tangential view. Measurements were compared between the 2 groups (with and without PFI).Knees with PFI were divided into 3 subgroups based on their treatment (group A: surgical valgus correction, group B: surgical soft tissue procedures for PFI, and group C: conservative treatment). Preoperative radiographs were used for the surgical group and last available radiographs were used for the conservative group. Clinical and radiographic data were compared between the groups. For groups A and B, clinical and radiographic data were also compared between preoperative and last visits. RESULTS: Of the 581 children with Down syndrome, 5% (31 children: 22 females, 9 males) had PFI in 56 knees. Mean age at diagnosis was 11.5±3.5 years. Of the remaining 550 children, 75 children had radiographs for 130 knees. Knees with PFI had significantly more valgus and a larger distal femoral physis-joint angle. Depression of the medial tibial plateau and lateral tibial translation were noted in knees with PFI. Insall-Salvati ratio was higher and the sulcus angle was larger in the PFI group.Of the 56 knees with PFI; 10 knees were in group A, 11 knees in group B, 33 knees in group C, and the remaining 2 knees had combined procedures. Preoperative mechanical and anatomic lateral distal femoral angles were smaller in group A than in group B or C. Grades of PFI improved in group B after surgery. This improvement was not noted in group A. CONCLUSIONS: In children with Down syndrome, different variations of the knee anatomy can be found. Although PFI might be the most evident knee abnormality, other underlying deformities are common. Treatment of the PFI should be planned through a comprehensive anatomic approach that addresses all aspects of knee deformity. LEVEL OF EVIDENCE: Level IV-prognostic and therapeutic study.


Assuntos
Síndrome de Down/complicações , Deformidades Congênitas dos Membros , Procedimentos Ortopédicos , Articulação Patelofemoral , Adolescente , Criança , Feminino , Lâmina de Crescimento , Humanos , Deformidades Congênitas dos Membros/complicações , Deformidades Congênitas dos Membros/diagnóstico , Masculino , Procedimentos Ortopédicos/métodos , Procedimentos Ortopédicos/estatística & dados numéricos , Avaliação de Processos e Resultados em Cuidados de Saúde , Articulação Patelofemoral/anormalidades , Articulação Patelofemoral/diagnóstico por imagem , Radiografia/métodos , Estudos Retrospectivos
3.
Pediatr Neurosurg ; 53(1): 1-6, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-28866663

RESUMO

BACKGROUND/AIMS: The physiological interaction between the intrathecal baclofen (ITB) delivery system and the ventriculoperitoneal (VP) shunting system in a patient who had both systems implanted has not been reported previously. The aim of our report is to evaluate the effect that one system's infection might have on the other. METHODS: Records of children who were followed at our institution between 2004 and 2015 for management of their ITB systems were reviewed. In this group, children who had VP shunts were identified, and those who had any of their ITB or VP systems infected were included. RESULTS: Out of 313 children managed with ITB therapy at our institution, 31 (24%) children had VP shunts. Two patients had infection in both systems, and 3 patients had infection in 1 system. CONCLUSION: This report suggests that if aspiration from both systems showed positive cultures, the treatment would be removal of both systems. If the primarily not infected system does not show positive cultures, it does not need to be removed. Close follow-up is recommended, and any sign of infection or malfunction of the primarily not infected device should be approached with a high level of suspicion.


Assuntos
Baclofeno/administração & dosagem , Contaminação de Equipamentos/prevenção & controle , Bombas de Infusão Implantáveis/microbiologia , Relaxantes Musculares Centrais/administração & dosagem , Derivação Ventriculoperitoneal , Adolescente , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Recém-Nascido , Bombas de Infusão Implantáveis/normas , Injeções Espinhais/normas , Masculino , Derivação Ventriculoperitoneal/normas , Adulto Jovem
4.
J Pediatr Orthop B ; 26(4): 383-387, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27548438

RESUMO

This study reports the recent experience in the management of scoliosis in Down's syndrome. Curve patterns, progression in brace, and surgical outcomes were recorded. Cardiac surgery history was compared between children with and without scoliosis. Out of 581 children with Down's syndrome, 62 children had scoliosis. The mean age of the children was 13.8 years. The mean magnitude was 31°. Bracing was successful in five of seven patients. Ten children had posterior spinal fusion with follow-up of 2.6 years (1-7.3). One deep wound infection was recorded with no revision. No difference was found in cardiac surgery history between children with and without scoliosis. LEVEL OF EVIDENCE: Type IV - prognostic and therapeutic study.


Assuntos
Síndrome de Down/complicações , Escoliose/cirurgia , Adolescente , Braquetes , Estudos de Casos e Controles , Criança , Feminino , Humanos , Masculino , Radiografia , Estudos Retrospectivos , Escoliose/complicações , Escoliose/diagnóstico por imagem , Fatores Sexuais , Fusão Vertebral , Resultado do Tratamento
5.
Rev. colomb. ortop. traumatol ; 25(2)jun. 2011. ilus
Artigo em Espanhol | LILACS | ID: lil-639092

RESUMO

Las plicas sinoviales de la articulación radiocapitelar pueden causar crepitación dolorosa de la articulación del codo y se deben diferenciar de otras causas de crepitación dolorosa del codo como los cuerpos libres intraarticulares, la inestabilidad o la luxación medial de la cabeza del tríceps sobre el epicóndilo medial. El dolor sobre la cara lateral del codo, acompañado de sensación de resalto en flexión y pronación, es un hallazgo común en los pacientes con dicha patología. El tratamiento con cirugía artroscópica del codo generalmente confirma la presencia de la plica sinovial asociada a un área adyacente de sinovitis y una lesión del cartílago de la cabeza radial y el capitelo. Se presenta el caso de una paciente joven con una plica sinovial dolorosa con una condromalacia radiocapitelar asociada.


Assuntos
Condromatose , Articulação do Cotovelo , Membrana Sinovial , Sinovite
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